β-catenin (CTNNB1) is an oncogenic transcription factor that is important in cell-cell adhesion and transcription of cell proliferation and survival genes that drive the pathogenesis of many different types of cancers. However, direct pharmacological targeting of CTNNB1 has remained challenging. Here, we have performed a screen with a library of cysteine-reactive covalent ligands to identify the monovalent degrader EN83 that depletes CTNNB1 in a ubiquitin-proteasome-dependent manner. We show that EN83 directly and covalently targets CTNNB1 three cysteines C466, C520, and C619, leading to destabilization and degradation of CTNNB1. Through structural optimization, we generate a highly potent and relatively selective destabilizing degrader that acts through the targeting of only C619 on CTNNB1. Our results show that chemoproteomic approaches can be used to covalently target and degrade challenging transcription factors like CTNNB1 through destabilization-mediated degradation.
Covalent Degrader of the Oncogenic Transcription Factor β-Catenin.
致癌转录因子β-catenin的共价降解剂
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作者:Gowans Flor A, Forte Nafsika, Hatcher Justin, Huang Oscar W, Wang Yangzhi, Altamirano Poblano Belen E, Wertz Ingrid E, Nomura Daniel K
| 期刊: | Journal of the American Chemical Society | 影响因子: | 15.600 |
| 时间: | 2024 | 起止号: | 2024 Jun 6 |
| doi: | 10.1021/jacs.4c05174 | 研究方向: | 肿瘤 |
| 信号通路: | Wnt/β-Catenin | ||
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