基因
抗药性
机制(生物学)
突变
抗性(生态学)
计算生物学
癌症研究
后天抵抗
医学
材料科学
生物
化学
遗传学
生物信息学
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2026-04-01
卷期号:16 (4): 620-622
标识
DOI:10.1158/2159-8290.cd-26-0153
摘要
The study by Fece de la Cruz, Varkaris, and colleagues uncovered a critical mechanism underlying resistance to the p53-Y220C reactivator rezatapopt in the PYNNACLE clinical trial. Specifically, rezatapopt treatment was shown to select for secondary mutations in the TP53 gene on the Y220C-mutant background, thereby abrogating its therapeutic efficacy. See related article by Fece de la Cruz et al., p. 677.
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