ZEBRAFISH IN DRUG DISCOVERY

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  • SCIENCE & TECHNOLOGY

    ZEBRAFISH IN DRUG DISCOVERY

    ACS MEETING NEWS: Small fish can impact drug and target screening in a big way

    CARMEN DRAHL, C&EN WASHINGTON

    ZEBRAFISH, little freshwater tropical fish that populate pet-store aquariums, are making a splash in several arenas of drug discovery research.

    Chemists' burgeoning interest in using zebrafish to complement other animal models and cell-based assays motivated an afternoon session sponsored by the Divi-sion of Chemical Toxicology at the Ameri-can Chemical Society national meeting in Boston last month, according to organizer Peter C. Dedon, a professor of toxicology and biological engineering at Massachu-setts Institute of Technology.

    The session demonstrated the utility of zebrafish in a wide range of applications in drug discovery. Participants chronicled their use of zebrafish to assess drug toxicity and

    efficacy, to find bioactive small molecules, and even to find genes coding for potential new drug targets. Speakers advised against drawing too many parallels between results in zebrafish and expectations in humans and other mammals, however, without the proper experimental evidence. "This eclec-tic group of zebrafish experts brings a lot of perspective for those who want to learn more about new model systems for drug and toxicity testing," Dedon said.

    Interest in using zebrafish is on the rise for several reasons. Zebrafish are small and inexpensive to maintain, and they produce hundreds of offspring in every mating, eas-ily accumulating statistically significant numbers of animals. What's more, zebra-fish embryos are transparent and develop

    SWIMMING WITH THE FISHES Zebrafish embryos can be housed in individual microplate wells for live-animal assays.

    outside the uterus, making it easy to monitor developing fish. In fact, zebrafish embryos are tiny enough to be raised in microplate wells for high-throughput whole-animal assays.

    Many test compounds can diffuse into ze-brafish embryos, simplifying drug adminis-tration. Researchers can also readily identi-fy zebrafish with gene mutations. Lastly, as vertebrates, zebrafish and other fish have most of the same organs and organ systems that mammals do, making them more rele-vant in whole-animal assays than fruit flies or roundworms, which have also been used in early drug discovery screening.

    Without the complex physiological en-vironment of an intact organism, in vitro tests, such as cell- or tissue-based assays, may not always be representative of the in vivo response. Drug action involves metab-olism, as well as interplay among different tissues. Zebrafish present a practical op-tion to conduct high-throughput screening in a whole organism at a very early stage of drug discovery.

    ALONG THESE LINES, Leonard I. Zon, director of the stem cell program at Children's Hospital Boston, described at the meeting how his lab has used zebra-fish to scour massive compound libraries for a specific biological outcome. Zon, a hematology/oncology specialist, sought a compound that could increase blood stem cell numbers. "Many patients who have leukemia get a cord blood transplant, but there aren't many stem cells in a cord," he said. That means the precious cells are less likely to take hold, especially in adult leuke-mia patients. "A way to amplify cord blood stem cells even twofold could dramatically increase the chances of a successful trans-plant," Zon explained.

    His team exposed zebrafish embryos to a 2,500-compound library and found that precursors to the lipid prostaglandin E2 increased zebrafish's blood stem cell num-bers, whereas nonsteroidal anti-inflamma-tory drugs that block prostaglandin synthe-

    "In part because of breakthroughs in zebrafish technology, which allow rapid and precise genetic

    control, interest in zebrafish as a model is surging."

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    sis decreased the number of blood stem cells. Importantly, the team was able to extend these results to adult zebrafish and validate the results in mice. The researchers now are planning a clinical trial.

    Jacqueline Lees, a biology professor at MIT, put zebrafish produced by her MIT colleague Nancy Hopkins to use in another screen, in this case searching for new cancer and cell cycle control genes. Lees described her search, which involved sifting through a library of zebrafish embryos with precisely generated and cata-loged mutations. "It is in part because of breakthroughs in zebra-fish technology, which allow rapid and precise genetic control, that the interest in zebrafish as a model is surging," commented Dedon. Lees's group searched for mutations that lead to visible external tumors or a shorter life span. Sure enough, the screen turned up eight genes that predispose fish to tumors, one of which was a ze-brafish relative of a known mammalian tumor suppressor gene.

    CAGES OR TANKS? Zebrafish are an economical, efficient complement to

    lab mice for researchers

    LAB MOUSE ZEBRAFISH Average life span ,l-3;years 1-3 years Age of sexual maturity irlV2 months - . 2-3 months Embryos per mating 1-10 'x - . . 100-300 Gestation period ;l9-21days ' . , 5 days Adult weight :20g - * . . 0.5-0.75 g Maintenance cost per day $L00" $0.01

    SOURCES: Jackson Laboratory, Phylonix

    Traversing the drug discovery landscape from a gene to a drug target is no easy task, but this technology has potential to contrib-ute to the search, according to Dedon. "Lees's research is laying the foundation that will be relevant to the drug industry in the future," Dedon said.

    After large-scale compound screens yield a few hits, it's impor-tant to collect data on drug toxicity and efficacy as early in the drug development process as possible to avoid costly, late-stage derail-ing of a promising drug candidate. Patricia McGrath, president and chief executive officer of Cambridge, Mass.-based contract research firm Phylonix Pharmaceuticals, and her colleagues have come up with ways to get this information out of zebrafish.

    At the Boston meeting, McGrath described a variety of tech-niques for quantifying drug effects rapidly and precisely in specific organs and tissues. Some of the tests seemed plucked right out of a hospital emergency room. For example, zebrafish electrocardio-grams (ECGs) are handy for gauging drugs' cardiovascular effects. "We only need two electrodes as opposed to four," said McGrath, referring to differences in the number of chambers in a zebrafish's heart and a human's. "The zebrafish ECG pattern is very similar to ours," she added.

    It's not unexpected that a zebrafish's heart might be similar to a person's, but it's a little more surprising that scrutinizing a fish might help cancer patients prevent the hearing loss associated with many cancer treatments. It so happens that zebrafish have clusters of sensory hair cells spanning their bodies, and these cells, which help fish gather in schools and fend off predators, are similar to human inner ear hair cells.

    Researchers at Phylonix exploited the fact that zebrafish em-bryos are clear and found a specific stain for the sensory hair cells

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  • SCIENCE & TECHNOLOGY

    FINGER ON THE PULSE It takes only two electrodes to get an electrocardiogram of a zebrafish.

    that makes it easy to monitor live fish for changes in these cells. The researchers administered chemo-therapeutic agents to the fish and ob-served hair cell loss, but they were able to prevent that loss by pretreating the fish with known protec-tive compounds. These results validate the test as a way to evaluate both the toxicity of new oncology drugs and the protective properties of new agents for preventing hearing loss.

    Screens such as these form the back-bone of Phylonix' recent contract with the Environmental Protection Agency's Tox-

    | Cast project, which 2 aims to assess new ways to characterize

    and pinpoint toxic-ity (G&EN, Aug. 6, page 34; C&EN Online Latest News, Aug. 8). Zebrafish screens are the only whole-animal assays that EPA has selected for ToxCast, illustrating the growing interest in using zebrafish to predict effects and toxicities of com-pounds in humans.

    Sometimes it isn't the drug candidate

    itself that's toxic, but its breakdown products. Cytochrome P450S are the major oxidative enzymes involved in drug metabolism. These enzymes chemically modify and degrade drugs, usually by inserting an oxygen atom into the drug molecule. In Boston, John Stegeman of Woods Hole Ocanographie Institution described his efforts to compare

    zebrafish cytochrome P450 genes with those of other animals. He cautioned that there is not always a direct matchup between P450 genes in zebrafish and in mammals.

    THE IMPLICATIONS of Stegeman's con-clusions are critical to metabolism stud-ies that rely on zebrafish-based assays, according to Fred Guengerich, chair of the ACS Division of Chemical Toxicology and a cytochrome P450 expert at Van-derbilt University. "If you see toxicity in zebrafish, and it is related to metabolism, the result may or may not be the same in people," he said.

    Zebrafish are an up-and-coming com-plement to the drug discovery arsenal. Ul-timately, however, the fish's strengths for drug discovery research must be matched by the potential of the research results to translate into contexts relevant to humans, according to Guengerich. "The real value of using zebrafish as a model is as a way to define molecular mechanisms, and this is information that we can use intelligently in mammals, ultimately on human systems," he said.

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    ZEBRAFISH IN DRUG DISCOVERY

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