Wang Zhenjie, Che Siyao, Yu Zhiqiang
Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, PR China; Office of Drug Clinical Trials, The People's Hospital of Gaozhou, Maoming, 525200, PR China.
Hepatological Surgery Department, The People's Hospital of Gaozhou, Maoming, 525200, PR China.
Eur J Pharm Sci. 2024 Jul 1;198:106793. doi: 10.1016/j.ejps.2024.106793. Epub 2024 May 11.
The revolutionary Proteolysis Targeting Chimera (PROTACs) have the exciting potential to reshape the pharmaceutical industry landscape by leveraging the ubiquitin-proteasome system for targeted protein degradation. Breast cancer, the most prevalent cancer in women, could be treated using PROTAC therapy. Although substantial work has been conducted, there is not yet a comprehensive overview or progress update on PROTAC therapy for breast cancer. Hence, in this article, we've compiled recent research progress focusing on different breast cancer target proteins, such as estrogen receptor (ER), BET, CDK, HER2, PARP, EZH2, etc. This resource aims to serve as a guide for future PROTAC-based breast cancer treatment design.
革命性的蛋白酶靶向嵌合体(PROTACs)具有令人兴奋的潜力,可通过利用泛素-蛋白酶体系统实现靶向蛋白质降解,从而重塑制药行业格局。乳腺癌是女性中最常见的癌症,可使用PROTAC疗法进行治疗。尽管已经开展了大量工作,但尚未有关于PROTAC疗法治疗乳腺癌的全面概述或进展更新。因此,在本文中,我们汇总了针对不同乳腺癌靶蛋白(如雌激素受体(ER)、BET、细胞周期蛋白依赖性激酶(CDK)、人表皮生长因子受体2(HER2)、聚(ADP-核糖)聚合酶(PARP)、增强子结合蛋白z(EZH2)等)的最新研究进展。本资源旨在为未来基于PROTAC的乳腺癌治疗设计提供指导。