37
Chronic Myeloid Leukemia (CML) Matt Walter Markey Program October 21, 2014

Chronic Myeloid Leukemia (CML) - The Division of Biology ...dbbs.wustl.edu/curstudents/Documents/Markey/10-21-2014_Walter C… · Chronic Myeloid Leukemia (CML) Matt Walter ... Chronic

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Chronic Myeloid Leukemia(CML)

Matt WalterMarkey ProgramOctober 21 2014

CML paradigm for cancer treatment

bull Identify primary genetic abnormalitybull Develop an agent that targets that abnormality

bull Monitor for efficacybull Overcoming resistance

Chronic Myeloid Leukemia Session Overview

1 Matt Walter = Hematopoiesis overview2 Dan Link = Signaling animal models3 Peter Westervelt = Clinical overview 4 Steve Oh = Imatinib preclinicalclinical5 Geoff Uy = Imatinib resistance 6 Rizwan Romee = Bone marrow transplant 7 Jerry Radich = Guest speaker on CML8 Last class = round table lunch

Patient interviews

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

Hematopoiesis

Hematopoietic growth factor (HGF) signaling

NEJM (2006) 35419 p2034

ReceptorTyrosine Kinase(RTK)

(ABL non‐Receptor TK)

Frequent targets for mutation in leukemia

Classification of LeukemiasLymphoid Myeloid

CLLChronicLymphocytic Leukemia

CMLChronicMyeloid Leukemia

ALLAcuteLymphocytic Leukemia

AMLAcuteMyeloid Leukemia

10100000 1100000 2100000(~6000 newyear)

5100000

Acute = fast clinical progression Block in differentiation(weeks to months)

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

CML paradigm for cancer treatment

bull Identify primary genetic abnormalitybull Develop an agent that targets that abnormality

bull Monitor for efficacybull Overcoming resistance

Chronic Myeloid Leukemia Session Overview

1 Matt Walter = Hematopoiesis overview2 Dan Link = Signaling animal models3 Peter Westervelt = Clinical overview 4 Steve Oh = Imatinib preclinicalclinical5 Geoff Uy = Imatinib resistance 6 Rizwan Romee = Bone marrow transplant 7 Jerry Radich = Guest speaker on CML8 Last class = round table lunch

Patient interviews

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

Hematopoiesis

Hematopoietic growth factor (HGF) signaling

NEJM (2006) 35419 p2034

ReceptorTyrosine Kinase(RTK)

(ABL non‐Receptor TK)

Frequent targets for mutation in leukemia

Classification of LeukemiasLymphoid Myeloid

CLLChronicLymphocytic Leukemia

CMLChronicMyeloid Leukemia

ALLAcuteLymphocytic Leukemia

AMLAcuteMyeloid Leukemia

10100000 1100000 2100000(~6000 newyear)

5100000

Acute = fast clinical progression Block in differentiation(weeks to months)

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Chronic Myeloid Leukemia Session Overview

1 Matt Walter = Hematopoiesis overview2 Dan Link = Signaling animal models3 Peter Westervelt = Clinical overview 4 Steve Oh = Imatinib preclinicalclinical5 Geoff Uy = Imatinib resistance 6 Rizwan Romee = Bone marrow transplant 7 Jerry Radich = Guest speaker on CML8 Last class = round table lunch

Patient interviews

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

Hematopoiesis

Hematopoietic growth factor (HGF) signaling

NEJM (2006) 35419 p2034

ReceptorTyrosine Kinase(RTK)

(ABL non‐Receptor TK)

Frequent targets for mutation in leukemia

Classification of LeukemiasLymphoid Myeloid

CLLChronicLymphocytic Leukemia

CMLChronicMyeloid Leukemia

ALLAcuteLymphocytic Leukemia

AMLAcuteMyeloid Leukemia

10100000 1100000 2100000(~6000 newyear)

5100000

Acute = fast clinical progression Block in differentiation(weeks to months)

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

Hematopoiesis

Hematopoietic growth factor (HGF) signaling

NEJM (2006) 35419 p2034

ReceptorTyrosine Kinase(RTK)

(ABL non‐Receptor TK)

Frequent targets for mutation in leukemia

Classification of LeukemiasLymphoid Myeloid

CLLChronicLymphocytic Leukemia

CMLChronicMyeloid Leukemia

ALLAcuteLymphocytic Leukemia

AMLAcuteMyeloid Leukemia

10100000 1100000 2100000(~6000 newyear)

5100000

Acute = fast clinical progression Block in differentiation(weeks to months)

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Hematopoietic growth factor (HGF) signaling

NEJM (2006) 35419 p2034

ReceptorTyrosine Kinase(RTK)

(ABL non‐Receptor TK)

Frequent targets for mutation in leukemia

Classification of LeukemiasLymphoid Myeloid

CLLChronicLymphocytic Leukemia

CMLChronicMyeloid Leukemia

ALLAcuteLymphocytic Leukemia

AMLAcuteMyeloid Leukemia

10100000 1100000 2100000(~6000 newyear)

5100000

Acute = fast clinical progression Block in differentiation(weeks to months)

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Classification of LeukemiasLymphoid Myeloid

CLLChronicLymphocytic Leukemia

CMLChronicMyeloid Leukemia

ALLAcuteLymphocytic Leukemia

AMLAcuteMyeloid Leukemia

10100000 1100000 2100000(~6000 newyear)

5100000

Acute = fast clinical progression Block in differentiation(weeks to months)

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

TerminallydifferentiatedBlood

ChronicMyeloidLeukemia(CML)

ChronicLymphocyticLeukemia(CLL)

EssentialThrombocytosis(ET)

PolycythemiaVera(PV)

Chronic Myelo‐MonocyticLeukemia(CMML)

Myeloproliferative Neoplasms (MPN)

Chronic Leukemias amp MPNs differentiation occurs

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

EssentialThrombocytosis(ET) (JAK2)

PolycythemiaVera(PV) (JAK2)

ChronicMyeloidLeukemia(CML) (BCRABL)

Genetics of Myeloproliferative Neoplasms (MPN)

Mastocytosis(KIT)

MyeloidNeoplasm withEosinophilia(PDGFRAB)

Mutationrearrangement of tyrosine kinase genes

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

CMLbull 141 () average age 45bull Increased blood WBC (gt25kuL) bull Minimalno fibrosis or dysplasia

Westervelt

Granulocyte maturation

Normal peripheral blood

Peter Maslak ASH Image Bank 2011 2011-1083

CML blood

Normal BM

basophil

eosinophil

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

CML chronic Blastic phase(block in differentiation)

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

CMLbull Chronic phasendash Driven by BCR‐ABLndash 50 no symptoms found on routine CBC

ndash uarrWBC PB BM spleenndash Fatigue weight loss abdominal fullness bleeding sweats large spleenliver

ndash 75 had accelerated phase 3‐18 months prior to blastic phase

bull Blast phasendash Acquire secondary mutations

ndash 13 = ALL 23 = AMLndash Decreased response to treatment and duration not long lasting

Westervelt

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

BCRABL fusion in CML

bull Cytogenetics = t(922) Philadelphia chromosome + (Ph+) (100 BCR‐ABLtranscript)

bull BCR‐ABL transcript +

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Tjio reports 46 chromosomes = normal

ldquodark agesrdquoTechnical problems

Flemming draws first chromosome

Waldeyer coins ldquochromosomerdquo

Painter reports 48 chromosomes = normal

1 better cultures2 hypotonic solution3 colchicine

Down+21

syndromes

TurnerXOKlinefelterXXY

1890

von Hansemann observesmitotic aberrations in tumor cells

1960

Nowell amp Hungerford = Ph chromosome amp CML

ldquoThe findings suggest a causal relationship between the chromosomal abnormality observed and chronic granulocytic leukemiardquo

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

1973

Rowley reportsPh chr = t(922)

1960

Nowell amp Hungerford = Ph chromosome amp CML

1983‐84 1998‐2001

Druker uses Gleevec to treat CML

Heisterkamp Stephenson Groffen Grosveld clone genes at breakpoints (BCR ABL)

Chromosome Gene Drug

Baltimore v‐Abl1980

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

v‐ABL oncogene

Lymphosarcoma virus‐induced thymic‐independent disease in miceAbelson HT Rabstein LS Cancer Res 1970 Aug30(8)2213‐22

Cell 1979 Dec18(4)955‐62

Cell 1980 Dec22(3)777‐85

v‐Abl

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

ndash p190 = 20‐30 ALL (most B‐cell)ndash p210 (p230) = 99 CML

bull ABL = Loss of N‐terminal Cap region of ABL normally inhibits kinase activity

bull BCR = Gain coil‐coil of BCR allows dimerization of BCR‐ABLndash Results in constitutive activation of the ABL tyrosine kinase

ndash Effects on cellular proliferation survival and motilityDan Link

(coil‐coil)

Heisterkamp Oncogene 2002 21(56)8536‐40

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Bone Marrow Cells

Semi-solid media(methylcellulose)

Culture with specific growth factors for 7-14 days

CFU-GM(GM-CSF)

BFU-E(Epo)

Colony‐forming Cell Assay (progenitors)

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Methylcellulose cultures

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Hematopoietic Stem Cell Assaysbull HSC Definition capable of long‐term (6 months) repopulation of ALL hematopoietic lineages

bull Bone marrow transplantation (gold standard)ndash Xenotransplantation models to assay human HSC

bull Long term culture‐initiating cell (LTC‐IC) assay

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID miceNODSCID gamma (NSG)

(immunodeficient)

Analyze after 3-6 months for blood cells

Mousehematopoietic donor cells (CD452)

congenic recipient mice

(CD451)

Analyze after 3-6 months for blood cells

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Better assays needed to study hematopoiesis

bull Methylcellulose and transplant assays are still the gold standard but is there a faster cheaper way to study these cells

bull How can you prospectively identify the cells and isolate them to study

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Flow cytometry

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

radiation

Murine or Xenotransplantation

Human hematopoietic cells

NODSCID mice(immunodeficient)

Analyze after 3-6 months for blood cells

CD34+ xenotransplant assays = 15000 HSCsCD34+CD38- = 1617 HSCs

Mousehematopoietic cells

congenic mice(CD451CD452)

Kit+Lineage-Sca+ (KLS) cells = 110 HSCsCD150+CD48- (SLAM) cells = 12 HSCs

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

GOALS 1) prospectively identify cells using flow cytometry (Weissman group = 1st mouse 2nd human hematopoiesis) 2) Define what cell is transformed in CML (chronic phase and blast crisis)

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

929 citations

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

288 single cells of each type

CMP MEP GMPCMP

MEP

GMP No Epo+Tpo

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

200 cells each

Cytospin of 5 pooled colonies

CMP MEP GMP

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

1000 cells on stroma

Single cell sorted

Lineage commitment at CMP single cell level

CMP

MEP

GMP

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Regulation of Hematopoiesis

bull Transcription factorsndash Regulate RNA expression of target genesndash Critical determinants of lineage commitment and terminal differentiation

bull Frequent targets for mutation in leukemia

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

PNAS (2002)9918 p11872

HUMAN PROGENITOR ASSAY

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

NEJM (2006) 35419 p2034

Stem cell

Progenitors

Terminallydifferentiated

Bonemarrow

Blood

What cell is transformed in CML

Link

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Lancet (2007)370 p342

CML therapyOhUyRomeeRadich

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Targeted therapy (chronic phase)bull Imatinib = discovered in high‐throughput screen of kinase inhibitors

NEJM 2003 Oct 9349(15)1399‐401

WesterveltOhUyRadich

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues

Issues

bull Cure vs control of chronic phase CMLbull Resistance in chronic phase CMLbull Treatment of blastic phase CML

  • Chronic Myeloid Leukemia(CML)
  • CML paradigm for cancer treatment
  • Chronic Myeloid Leukemia Session Overview
  • Slide Number 4
  • Hematopoietic growth factor (HGF) signaling
  • Slide Number 6
  • Chronic Leukemias amp MPNs differentiation occurs
  • Genetics of Myeloproliferative Neoplasms (MPN)
  • CML
  • Slide Number 10
  • CML
  • BCRABL fusion in CML
  • Slide Number 13
  • Slide Number 14
  • Slide Number 15
  • Slide Number 16
  • Slide Number 17
  • Slide Number 18
  • Methylcellulose cultures
  • Hematopoietic Stem Cell Assays
  • Slide Number 21
  • Better assays needed to study hematopoiesis
  • Flow cytometry
  • Slide Number 24
  • Slide Number 25
  • Slide Number 26
  • Slide Number 27
  • Slide Number 28
  • Slide Number 29
  • Regulation of Hematopoiesis
  • Slide Number 31
  • Slide Number 32
  • Slide Number 33
  • Slide Number 34
  • CML therapy
  • Targeted therapy (chronic phase)
  • Issues