The Molecular Basis of Ubiquitin-Conjugating Enzymes (E2s) as a Potential Target for Cancer Therapy

被引:33
作者
Du, Xiaodi [1 ]
Song, Hongyu [1 ]
Shen, Nengxing [1 ]
Hua, Ruiqi [1 ]
Yang, Guangyou [1 ]
机构
[1] Sichuan Agr Univ, Coll Vet Med, Dept Parasitol, Chengdu 611130, Peoples R China
基金
中国国家自然科学基金;
关键词
ubiquitin-conjugating enzymes; E2s; cancer; target; NF-κ B; inhibitors; NF-KAPPA-B; EPITHELIAL-MESENCHYMAL TRANSITION; PROMOTES GASTRIC-CANCER; FANCONI-ANEMIA PATHWAY; CELL LUNG-CANCER; WNT/BETA-CATENIN; TNF-ALPHA; COLORECTAL-CANCER; DNA-REPAIR; K11-LINKED POLYUBIQUITINATION;
D O I
10.3390/ijms22073440
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
Ubiquitin-conjugating enzymes (E2s) are one of the three enzymes required by the ubiquitin-proteasome pathway to connect activated ubiquitin to target proteins via ubiquitin ligases. E2s determine the connection type of the ubiquitin chains, and different types of ubiquitin chains regulate the stability and activity of substrate proteins. Thus, E2s participate in the regulation of a variety of biological processes. In recent years, the importance of E2s in human health and diseases has been particularly emphasized. Studies have shown that E2s are dysregulated in variety of cancers, thus it might be a potential therapeutic target. However, the molecular basis of E2s as a therapeutic target has not been described systematically. We reviewed this issue from the perspective of the special position and role of E2s in the ubiquitin-proteasome pathway, the structure of E2s and biological processes they are involved in. In addition, the inhibitors and microRNAs targeting E2s are also summarized. This article not only provides a direction for the development of effective drugs but also lays a foundation for further study on this enzyme in the future.
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页数:28
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