成纤维细胞生长因子受体
PI3K/AKT/mTOR通路
癌症研究
蛋白激酶B
蛋白激酶结构域
激酶
药理学
信号转导
计算生物学
成纤维细胞生长因子
化学
生物信息学
受体
生物
细胞生物学
生物化学
基因
突变体
作者
Abhishek Tripathi,Daneng Li,Sumanta K. Pal
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2023-09-06
卷期号:13 (9): 1964-1965
被引量:1
标识
DOI:10.1158/2159-8290.cd-23-0728
摘要
Summary: Facchinetti and colleagues provide key insights into the evolution of resistance to fibroblast growth factor receptor (FGFR) inhibitors, including the development of kinase domain mutations and activation of the PI3K–AKT signaling axis. In a separate study, Subbiah and colleagues report extensive preclinical data and initial clinical data for RLY-4008, an FGFR2-selective inhibitor that is poised to minimize toxicity and overcome resistance through greater potency and selectivity. See related article by Facchinetti et al., p. 1998 (5). See related article by Subbiah et al., p. 2012 (7).
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