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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.

More information Original publication

DOI

10.1016/j.tips.2024.06.001

Type

Journal article

Publication Date

2024-08-01T00:00:00+00:00

Volume

45

Pages

723 - 738

Total pages

15

Keywords

oncology, pharmacology, physiology, readout, therapeutics, Humans, Drug Discovery, Neoplasms, Antineoplastic Agents, Phenotype, Animals, Drug Screening Assays, Antitumor