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
Mutations in epidermal growth factor receptor (EGFR) kinase domain consistently activate downstream signaling pathways, such as the PI3K/AKT/mTOR and RAS/RAF/MEK, thereby promoting tumor growth. Although the majority of non-small cell lung cancer (NSCLC) patients harboring EGFR mutations are sensitive to existing EGFR tyrosine kinase inhibitors (EGFR-TKIs), there remains an unmet clinical need for effective therapies targeting EGFR Ex20ins mutations, making direct targeting EGFR Ex20ins mutations a promising therapeutic strategy.
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