Recent advances in the development of Mcl-1 inhibitors for cancer therapy

被引:102
作者
Hird, Alexander W. [1 ]
Tron, Adriana E. [1 ]
机构
[1] AstraZeneca Boston, IMED Biotech Unit, Oncol, 35 Gatehouse Dr, Waltham, MA 02451 USA
关键词
Apoptosis; Protein-protein interactions; Mcl-1; BH-3 mimetic drugs; Drug development; Cancer; DEPENDENT KINASE INHIBITOR; ANTI-APOPTOTIC MCL-1; MULTIPLE-MYELOMA CELLS; DOWN-REGULATION; ACQUIRED-RESISTANCE; SIGNALING PATHWAY; FAMILY PROTEINS; HIGH-AFFINITY; BCL-2; SURVIVAL;
D O I
10.1016/j.pharmthera.2019.02.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dysregulation of the mitochondrial apoptotic pathway controlled by members of the Bcl-2 protein family plays a central role in cancer development and resistance to conventional cytotoxic as well as targeted therapies. Hence, selective inhibition of pro-survival Bcl-2 family of proteins to activate apoptosis in malignant cells represents an exciting anti-cancer strategy. The remarkable clinical performance of the selective Bcl-2 antagonist venetoclax has highlighted the potential for selective inhibitors of the other pro-survival members of the Bcl-2 family, particularly Mc1-1. Here we review the latest progress on the discovery and development of selective inhibitors of Mc1-1 that are undergoing clinical evaluation for cancer therapy. (C) 2019 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:59 / 67
页数:9
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