The design and development of covalent protein-protein interaction inhibitors for cancer treatment

被引:71
|
作者
Cheng, Sha-Sha [1 ]
Yang, Guan-Jun [1 ]
Wang, Wanhe [2 ,3 ]
Leung, Chung-Hang [1 ]
Ma, Dik-Lung [2 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Hong Kong Baptist Univ, Dept Chem, Kowloon, Hong Kong 999077, Peoples R China
[3] Northwestern Polytech Univ, Inst Med Res, Xian 710072, Peoples R China
基金
中国国家自然科学基金;
关键词
Protein-protein interaction; Covalent inhibitors; Cancer therapy; SMALL-MOLECULE INHIBITORS; DRUG DISCOVERY; SELECTIVE-INHIBITION; BINDING-SITES; POTENT; IDENTIFICATION; REACTIVITY; CYSTEINE; MECHANISM; DATABASE;
D O I
10.1186/s13045-020-00850-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Protein-protein interactions (PPIs) are central to a variety of biological processes, and their dysfunction is implicated in the pathogenesis of a range of human diseases, including cancer. Hence, the inhibition of PPIs has attracted significant attention in drug discovery. Covalent inhibitors have been reported to achieve high efficiency through forming covalent bonds with cysteine or other nucleophilic residues in the target protein. Evidence suggests that there is a reduced risk for the development of drug resistance against covalent drugs, which is a major challenge in areas such as oncology and infectious diseases. Recent improvements in structural biology and chemical reactivity have enabled the design and development of potent and selective covalent PPI inhibitors. In this review, we will highlight the design and development of therapeutic agents targeting PPIs for cancer therapy.
引用
收藏
页数:14
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