Progress in the Discovery of Small Molecule Modulators of DeSUMOylation

被引:11
作者
Chen, Shiyao [1 ]
Dong, Duoling [1 ]
Xin, Weixiang [1 ]
Zhou, Huchen [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai, Peoples R China
关键词
SUMO-SPECIFIC PROTEASE; SQUAMOUS-CELL CARCINOMA; UBIQUITIN E3 LIGASE; SUMOYLATION; SENP5; IDENTIFICATION; MODIFIER; CONJUGATION; GENE; INHIBITORS;
D O I
10.21775/cimb.035.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SUMOylation and DeSUMOylation are reversible protein post-translational modification (PTM) processes involving small ubiquitin-like modifier ( SUMO) proteins. These processes have indispensable roles in various cellular processes, such as subcellular localization, gene transcription, and DNA replication and repair. Over the past decade, increasing attention has been given to SUMO-related pathways as potential therapeutic targets. The Sentrin/SUMO-specific protease (SENP), which is responsible for deSUMOylation, has been proposed as a potential therapeutic target in the treatment of cancers and cardiac disorders. Unfortunately, no SENP inhibitor has yet reached clinical trials. In this review, we focus on advances in the development of SENP inhibitors in the past decade.
引用
收藏
页码:17 / 34
页数:18
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