Ludwig Institute for Cancer Research Ltd., Oxford, UK.
Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Nat Chem Biol. 2015 Dec;11(12):942-8. doi: 10.1038/nchembio.1963. Epub 2015 Nov 17.
The upswing in US Food and Drug Administration and European Medicines Agency drug approvals in 2014 may have marked an end to the dry spell that has troubled the pharmaceutical industry over the past decade. Regardless, the attrition rate of drugs in late clinical phases remains high, and a lack of target validation has been highlighted as an explanation. This has led to a resurgence in appreciation of phenotypic drug screens, as these may be more likely to yield compounds with relevant modes of action. However, cell-based screening approaches do not directly reveal cellular targets, and hence target deconvolution and a detailed understanding of drug action are needed for efficient lead optimization and biomarker development. Here, recently developed functional genomics technologies that address this need are reviewed. The approaches pioneered in model organisms, particularly in yeast, and more recently adapted to mammalian systems are discussed. Finally, areas of particular interest and directions for future tool development are highlighted.
2014 年,美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)批准的药物数量呈上升趋势,这可能标志着困扰制药行业过去十年的干旱期已经结束。尽管如此,晚期临床阶段药物的淘汰率仍然很高,缺乏目标验证已被认为是一个解释。这导致人们重新开始重视表型药物筛选,因为这些筛选方法更有可能产生具有相关作用模式的化合物。然而,基于细胞的筛选方法并不能直接揭示细胞靶标,因此需要对靶标进行分解,以及对药物作用有详细的了解,以实现有效的先导化合物优化和生物标志物开发。本文综述了最近开发的能够满足这一需求的功能基因组学技术。讨论了在模式生物(尤其是酵母)中开创的方法,以及最近在哺乳动物系统中采用的方法。最后,突出了特别关注的领域和未来工具开发的方向。