癌症研究
化学
细胞凋亡
磷酸化
突变
原癌基因蛋白质c-ret
激酶
后天抵抗
细胞生物学
药理学
细胞培养
癌症
作者
Gangpeng Yang,Xiaowen Niu,Xiaoxu Zhao,Mingjin Xu,Tingyao Li,Li Tan,Haowen Ma,Zhang Zhang,Qian Cai
标识
DOI:10.1021/acs.jmedchem.6c01861
摘要
Abstract Pharmacological invention of RET offers a compelling strategy to treat patients harboring RET fusions or mutations. Selective RET inhibitors, including pralsetinib and selpercatinib, have demonstrated substantial clinical benefits. However, this efficacy is often compromised by the occurrence of resistance, particularly RET solvent front mutations G810C/R. To address this problem, we performed a systematic structure−activity optimization based on our reported RET inhibitors. Our efforts yielded F73, a next generation RET inhibitor with potent activity against RET mutations including V804M and G810C/R. F73 effectively suppressed RET phosphorylation and downstream SHC activation in Ba/Fa3 cells harboring various RET resistance mutations. Furthermore, it induced apoptosis and cell-cycle arrest in a dose-dependent manner in CCDC6-RET and CCDC6-RET-G810R Ba/F3 cells. Notably, F73 exhibited robust antitumor efficacy in Ba/F3-RET-G810R xenograft models, outperforming selpercatinib, thus supporting its potential to overcome resistance mediated by RET gatekeeper (V804M) and solvent-front (G810C/R) mutations.
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