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Introduction to special issueAre We There Yet?Barbara R. Jasny and Leslie Roberts
In some cases, the roadblocks have arisen from the sheer complexity of the biology, as Couzin describes in a News story (p. 591). When the mutated BRCA genes were discovered in the mid-1990s, researchers thought they were close to solving the enigma of breast cancer. A decade later, that disease remains mysterious, but the BRCA genes are illuminating a network of defects that drive a variety of other cancers. Meanwhile, a report from the New York Breast Cancer Study Group (p. 643) and the associated Perspective (Levy-Lehad and Plon, p. 574) describe the genetic and nongenetic factors influencing the risk of breast cancer in a large cohort. Increasing evidence suggests that genetic changes may partially explain why people of different ancestry experience disease or metabolize drugs differently. But, as Holden reports in a News story (p. 594), scientists are sharply divided on whether such genetic clues are firm enough to guide medical practice. Even when the biology is clear and a gene test can help flag fatal drug reactions, as Marshall describes in a News story (p. 588), physicians may be reluctant to embrace the technology. In other areas, genomic knowledge is slowly wending its way into medical practice. For instance, researchers are using the rapidly expanding knowledge about the genomes of microorganisms to speed efforts to develop vaccines, as Rappuoli and Covacci (p. 602) describe, promising widespread benefits in the fight against infectious diseases. Molecular imaging is providing increasing power to studies of animal models of disease and is beginning to be used in clinical trials as a noninvasive means of monitoring disease progress and response to therapeutic agents (Herschman, p. 605). On the Signal Transduction Knowledge Environment Web site, Perspectives describe the therapeutic potential of antisense strategies (Opalinska and Gewirtz) and the application of microarray analysis to pharmacogenomics (Levy). Translating genomic information into successful clinical trials will require advances on several fronts. Despite extensive preclinical studies, the vast majority of clinical trials fail because the drugs don't work as anticipated in patients or lead to intolerable side effects. According to Duyk (p. 603), the lack of basic information about physiology is a major roadblock to predicting which drugs are likely to succeed. The payoff from genomics should benefit all nations, not just the rich. Some of these benefits are beginning to be felt in the developing world, notes Weatherall (p. 597), especially in regard to monogenic and infectious diseases. But we will not truly be "there" in genomic medicine until we have followed Sydney Brenner's prescription (p. 533) to "stand up for all humanity."
The editors suggest the following Related Resources on Science sites:In Science Magazine
In Science Signaling
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Science. ISSN 0036-8075 (print), 1095-9203 (online)