Biochemical &Cellular Pharmacology, Genentech, South San Francisco, California 94080, USA.
Discovery Sciences, Primary Pharmacology Group, Pfizer, Groton, Connecticut 06340, USA.
Nat Rev Drug Discov. 2017 Aug;16(8):531-543. doi: 10.1038/nrd.2017.111. Epub 2017 Jul 7.
Phenotypic drug discovery (PDD) approaches do not rely on knowledge of the identity of a specific drug target or a hypothesis about its role in disease, in contrast to the target-based strategies that have been widely used in the pharmaceutical industry in the past three decades. However, in recent years, there has been a resurgence in interest in PDD approaches based on their potential to address the incompletely understood complexity of diseases and their promise of delivering first-in-class drugs, as well as major advances in the tools for cell-based phenotypic screening. Nevertheless, PDD approaches also have considerable challenges, such as hit validation and target deconvolution. This article focuses on the lessons learned by researchers engaged in PDD in the pharmaceutical industry and considers the impact of 'omics' knowledge in defining a cellular disease phenotype in the era of precision medicine, introducing the concept of a chain of translatability. We particularly aim to identify features and areas in which PDD can best deliver value to drug discovery portfolios and can contribute to the identification and the development of novel medicines, and to illustrate the challenges and uncertainties that are associated with PDD in order to help set realistic expectations with regard to its benefits and costs.
表型药物发现(PDD)方法不依赖于对特定药物靶点身份的了解,也不依赖于对其在疾病中作用的假设,这与过去三十年来制药行业广泛使用的基于靶点的策略形成对比。然而,近年来,基于 PDD 方法有可能解决疾病中尚未完全理解的复杂性及其提供一流药物的承诺,以及基于细胞表型筛选的工具的重大进展,人们对 PDD 方法的兴趣再次高涨。然而,PDD 方法也存在相当大的挑战,例如命中验证和目标分解。本文重点介绍了制药行业从事 PDD 研究的研究人员所获得的经验教训,并考虑了“组学”知识在定义精准医学时代细胞疾病表型方面的影响,引入了可译性链的概念。我们特别旨在确定 PDD 能够为药物发现组合带来最佳价值的特征和领域,并有助于确定和开发新的药物,并说明与 PDD 相关的挑战和不确定性,以便帮助对其收益和成本设定现实的期望。