Small molecules targeting protein-protein interactions for cancer therapy

被引:28
|
作者
Wu, Defa [1 ,2 ,3 ]
Li, Yang [1 ,2 ,3 ]
Zheng, Lang [1 ,2 ,3 ]
Xiao, Huan [1 ,2 ,3 ]
Ouyang, Liang [1 ,2 ,3 ]
Wang, Guan [1 ,2 ,3 ]
Sun, Qiu [1 ,2 ,3 ,4 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Dept Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Innovat Ctr Nursing Res, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Sch Nursing, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, West China Med Publishers, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Protein-protein interactions; Cancer; Small molecules; Structure-activity relationships; STRUCTURE-BASED DESIGN; MICROTUBULE-STABILIZING AGENTS; NF-KAPPA-B; STRUCTURAL BASIS; C-MYC; MDM2; INHIBITOR; BINDING-SITES; CELL-DEATH; IAP PROTEINS; P53; PATHWAY;
D O I
10.1016/j.apsb.2023.05.035
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein-protein interactions (PPIs) are fundamental to many biological processes that play an important role in the occurrence and development of a variety of diseases. Targeting the interaction between tumour-related proteins with emerging small molecule drugs has become an attractive approach for treatment of human diseases, especially tumours. Encouragingly, selective PPI-based therapeutic agents have been rapidly advancing over the past decade, providing promising perspectives for novel therapies for patients with cancer. In this review we comprehensively clarify the discovery and development of small molecule modulators of PPIs from multiple aspects, focusing on PPIs in disease, drug design and discovery strategies, structure-activity relationships, inherent dilemmas, and future directions.
引用
收藏
页码:4060 / 4088
页数:29
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