化学
转移
细胞迁移
泛素连接酶
运动性
癌症研究
泛素
癌细胞
癌症
细胞生长
细胞
细胞生物学
生物化学
遗传学
生物
基因
作者
Jinxin Che,Zegao Jin,Fangjie Yan,Jieqiong You,Jiangfeng Xie,Binhui Chen,Gang Cheng,Hong Zhu,Qiaojun He,Yongzhou Hu,Bo Yang,Ji Cao,Xiaowu Dong
标识
DOI:10.1021/acs.jmedchem.1c00586
摘要
The gain of cell motility is an essential prerequisite for cancer metastasis. The ubiquitin ligase subunit WD repeat and SOCS box-containing 1 (WSB1) has been demonstrated to regulate hypoxia-driven tumor cell migration. However, there is still a lack of methods for discovering inhibitors targeting the WSB1 axis. Here, we employed phenotypic screening models and identified compound 4 that displayed migration inhibitory activity against WSB1-overexpressing cells. Further studies indicated that it may function as a WSB1 degrader, thus leading to the accumulation of the Rho guanosine diphosphate dissociation inhibitor 2 (RhoGDI2) protein, reversing the expression of downstream F-actin and formation of membrane ruffles, and disturbing the migration capacity of cancer cells. Moreover, compound 4 exhibited a promising in vivo anticancer metastatic effects. Our findings show the discovery of a new WSB1 degrader, providing a unique solution for the treatment of cancer metastasis.
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