微管蛋白
体内
化学
小脑
微管
蛋白酶体
体外
细胞培养
A549电池
药物发现
癌症研究
细胞生物学
泛素
生物化学
生物
泛素连接酶
遗传学
基因
作者
Hua Yang,Jinling Qin,Yuanyuan Pei,Sumeng Guan,Mei Zhao,Yingge Wang,Yongfang Yao,Yongtao Duan,Moran Sun
标识
DOI:10.1016/j.ejmech.2023.116067
摘要
Overexpression of β3-tubulin is a common occurrence in human tumors and is associated with resistance to microtubule-targeting agents. PROTAC strategy has demonstrated significant potential in overcoming drug resistance. Herein, we report the discovery of W13 as the first PROTAC against tubulin, which was created by connecting a CRBN ligand to the widely recognized microtubule-destabilizing agent CA-4. Notably, it retains the inhibitory activity of the parental CA-4 and further exhibits substantial degradation of α/β/β3-tubulin in both A549 and A549/Taxol cell lines. The degradation of tubulin was subsequently verified to be mediated by the ubiquitin-proteasome system. Importantly, tumor xenograft research clearly showed W13's promising antitumor activity against human lung cancer. Taken together, the discovery of W13 demonstrated the practicality and feasibility of PROTAC targeting tubulin, hence establishing a potential therapeutic approach for treating NSCLC caused by the overexpression of β3-tubulin.
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