自噬
程序性细胞死亡
体内
细胞
蛋白激酶B
医学
细胞生长
癌症研究
细胞培养
全景望远镜
细胞凋亡
细胞生物学
药理学
化学
生物
信号转导
组蛋白脱乙酰基酶
基因
组蛋白
遗传学
生物化学
生物技术
作者
Hui Lü,Wenying Fu,Yiqun Xia,Ying Yan,Chih-Hung Shu,Yinghua Chen,Chenxin Xu,Peisen Zheng,Xin Shen,Ri Cui,Peng Zou,Duojiao Ni
标识
DOI:10.1038/s41420-025-02657-9
摘要
Adagrasib, a KRASG12C inhibitor, recently received accelerated approval from the US FDA for the treatment of patients diagnosed with KRASG12C-mutated non-small cell lung cancer. Although adagrasib has demonstrated excellent clinical efficacy and good safety, the molecular mechanism underlying the antitumor activity of adagrasib remains elusive. Here, we report that adagrasib treatment markedly inhibited the growth of cells harboring the KRASG12C mutation, whereas the non-KRASG12C cell lines H1299 and PC-9 were also sensitive to adagrasib, indicating that adagrasib exerted off-target effects. Mechanism studies indicated that adagrasib treatment reduced the level of NRF2 via upregulating its ubiquitination, and NRF2 overexpression can reverse the adagrasib-induced cell death in H23 and H1299 cells. Furthermore, adagrasib treatment significantly increased the cellular ROS level and thereby activating autophagy and AKT signaling pathways in H23 and H1299 cells. Importantly, combination of adagrasib with panobinostat demonstrated enhanced antitumor activity in vitro and in vivo. Overall, our data elucidate a novel mechanism of adagrasib, which will be critical for the clinical application of adagrasib.
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