Wan Yichao, Dai Ningning, Tang Zilong, Fang Hao
Key Laboratory of Theoretical Organic Chemistry and Functional Molecule, Ministry of Education, Hunan Provincial Key Laboratory of Controllable Preparation and Functional Application of Fine Polymers, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan, Hunan 411201, PR China.
Department of Medicinal Chemistry, Key Laboratory of Chemical Biology, Ministry of Education, School of Pharmacy, Shandong University, Jinan, Shandong 250012, PR China.
Eur J Med Chem. 2018 Feb 25;146:471-482. doi: 10.1016/j.ejmech.2018.01.076. Epub 2018 Jan 31.
The anti-apoptotic members of B-cell lymphoma-2 (Bcl-2) proteins family, such as Bcl-2 and myeloid cell leukemia-1 (Mcl-1), are the key regulators of the intrinsic pathway of apoptosis and overexpressed in many tumor cells, which have been confirmed as potential drug targets for cancers. A number of Bcl-2 proteins inhibitors have been developed and conducted clinical trials, but no Mcl-1 inhibitors are presented in the clinics. In addition, Mcl-1 is an important reason for the resistance to radio- and chemotherapies, including inhibitors that target other Bcl-2 family members. For example, the recently launched Bcl-2-selective inhibitor ABT-199 displays highly potency in the treatment of chronic lymphocytic leukemia (CLL), but it cannot induce the apoptosis controlled by Mcl-1 in some tumor cell lines. Therefore, developing potent Mcl-1 inhibitors become urgently needed in clinical therapy. This review briefly introduces the structure of Mcl-1 protein, the role in cancers and focuses on the progress of small-molecule Mcl-1 inhibitors from 2012 to 2017.
B细胞淋巴瘤-2(Bcl-2)蛋白家族的抗凋亡成员,如Bcl-2和髓样细胞白血病-1(Mcl-1),是细胞凋亡内在途径的关键调节因子,在许多肿瘤细胞中过表达,已被确认为癌症的潜在药物靶点。许多Bcl-2蛋白抑制剂已被开发并进行临床试验,但临床上尚无Mcl-1抑制剂。此外,Mcl-1是对放疗和化疗产生耐药性的一个重要原因,包括针对其他Bcl-2家族成员的抑制剂。例如,最近推出的Bcl-2选择性抑制剂ABT-199在治疗慢性淋巴细胞白血病(CLL)方面显示出高效力,但它不能在某些肿瘤细胞系中诱导由Mcl-1控制的细胞凋亡。因此,开发有效的Mcl-1抑制剂在临床治疗中变得迫切需要。本文综述简要介绍了Mcl-1蛋白的结构、在癌症中的作用,并重点关注了2012年至2017年小分子Mcl-1抑制剂的研究进展。