Key Laboratory of Structure-Based Drugs Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
J Med Chem. 2024 Apr 25;67(8):5963-5998. doi: 10.1021/acs.jmedchem.3c01998. Epub 2024 Apr 10.
As a tripartite cell death switch, B-cell lymphoma protein 2 (Bcl-2) family members precisely regulate the endogenous apoptosis pathway in response to various cell signal stresses through protein-protein interactions. Myeloid leukemia-1 (Mcl-1), a key anti-apoptotic Bcl-2 family member, is positioned downstream in the endogenous apoptotic pathway and plays a central role in regulating mitochondrial function. Mcl-1 is highly expressed in a variety of hematological malignancies and solid tumors, contributing to tumorigenesis, poor prognosis, and chemoresistance, making it an attractive target for cancer treatment. This Perspective aims to discuss the mechanism by which Mcl-1 regulates apoptosis and non-apoptotic functions in cancer cells and to outline the discovery and optimization process of potent Mcl-1 modulators. In addition, we summarize the structural characteristics of potent inhibitors that bind to Mcl-1 through multiple co-crystal structures and analyze the cardiotoxicity caused by current Mcl-1 inhibitors, providing prospects for rational targeting of Mcl-1.
作为一个三方细胞死亡开关,B 细胞淋巴瘤蛋白 2(Bcl-2)家族成员通过蛋白质-蛋白质相互作用,精确调节内源性凋亡途径,以响应各种细胞信号应激。髓样白血病 1(Mcl-1)是内源性凋亡途径中的关键抗凋亡 Bcl-2 家族成员,在调节线粒体功能方面发挥核心作用。Mcl-1 在多种血液恶性肿瘤和实体瘤中高度表达,有助于肿瘤发生、预后不良和化疗耐药,使其成为癌症治疗的一个有吸引力的靶点。本观点旨在讨论 Mcl-1 调节癌细胞凋亡和非凋亡功能的机制,并概述强效 Mcl-1 调节剂的发现和优化过程。此外,我们总结了通过多个共晶体结构与 Mcl-1 结合的强效抑制剂的结构特征,并分析了当前 Mcl-1 抑制剂引起的心脏毒性,为 Mcl-1 的合理靶向提供了前景。