可药性
表型筛选
药物发现
计算生物学
表型
癌症
生物
疾病
药物开发
药品
生物信息学
医学
药理学
遗传学
基因
病理
作者
Wang Zhen-yi,Alžbeta Hulı́ková,Pawel Swietach
标识
DOI:10.1016/j.tips.2024.06.001
摘要
Before molecular pathways in cancer were known to a depth that could predict targets, drug development relied on phenotypic screening, where the effectiveness of candidate chemicals is judged from functional readouts without considering the mechanisms of action. The unraveling of tumor-specific pathways has brought targets for molecularly driven drug discovery, but precedents in the field have shown that awareness of pathways does not necessarily predict therapeutic efficacy, and many cancers still lack druggable targets. Phenotypic screening therefore retains a niche in drug development where a targeted approach is not informative. We analyze the unique advantages of phenotypic screens, and how technological advances have improved their discovery power. Notable advances include the use of larger biological panels and refined protocols that address the disease-relevance and increase data content with imaging and omic approaches.
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