Pharmacologically targeting tumor suppressors necessitates an unprecedented strategy of restoring, rather than conventionally inhibiting, protein function, and p53, the most commonly mutated protein in cancer, has thus remained undruggable. In this study, we address long-standing misconceptions in the field and gaps in the scientific logic for a p53 function-restoration strategy, identify four barriers for drugging mutant p53, and accordingly propose effectiveness evaluation criteria, clinical-translating norms, and prospects for mutant p53 rescue compounds. ©2024 American Association for Cancer Research.
Huaxin Song, Shujun Xiao, Jiaqi Wu, Min Lu. Drugging p53: Barriers, Criteria, and Prospects. Cancer discovery. 2024 Nov 01;14(11):2055-2060
PMID: 39485253
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