癌症研究
表皮生长因子受体
酪氨酸激酶
PI3K/AKT/mTOR通路
蛋白激酶结构域
表皮生长因子受体抑制剂
蛋白激酶B
靶向治疗
MAPK/ERK通路
医学
激酶
生物
信号转导
癌症
基因
内科学
遗传学
突变体
作者
Wenjian Zhu,Junping Pei,Xiaoyun Lu
标识
DOI:10.1080/13543776.2024.2446220
摘要
An increasing number of EGFR Ex20ins inhibitors are being developed and reported. Existing inhibitors are focused on enhancing the efficacy of EGFR Ex20ins inhibitors and addressing the challenge of targeted resistance by optimizing the second - or third-generation EGFR inhibitors and developing innovative skeleton molecules. Moreover, the development of targeted protein degraders, allosteric inhibitors, and combination therapies provide additional approaches to address EGFR Ex20ins mutations. However, bypass resistance, selectivity, and drug sensitivity still pose challenges in this field.
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