克拉斯
医学
癌症研究
突变体
可药性
内质网
病毒癌基因
腺癌
癌症
内科学
生物
细胞生物学
遗传学
基因
结直肠癌
作者
Jun Zhao,Yuanyuan Zeng,Andrew Z. Wang,Weina Zhang,Jiaying Li,Jingqiang Zhu,Zhihong Liu,J-a. Huang
标识
DOI:10.1016/j.jtho.2023.09.295
摘要
Kirsten rat sarcoma (KRAS) is a frequently mutated oncogene in lung adenocarcinoma (LUAD). Recently, KRASG12C was identified to be druggable and KRASG12C inhibitors such as sotorasib and adagrasib had shown great clinical application prospect. However, only KRASG12C inhibitors are clinically used recently, and diverse mechanisms may cause resistance to KRASG12C inhibitors, suggesting that it is urgent to develop new chemotherapeutic strategies based on the biological characteristics of pan-KRASG12 mutant LUAD.
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