The Emerging Role of Deubiquitinases in Radiosensitivity

被引:5
|
作者
Cao, Xiang [1 ,2 ]
Yan, Zhenyu [1 ,2 ]
Chen, Zihan [3 ]
Ge, Yizhi [1 ,2 ]
Hu, Xinyu [1 ,2 ]
Peng, Fanyu [1 ,2 ]
Huang, Wenxuan [1 ,2 ]
Zhang, Pingchuan [1 ,2 ]
Sun, Ruozhou [1 ,2 ]
Chen, Jiazhen [1 ,2 ]
Ding, Mingjun [1 ,2 ]
Zong, Dan [1 ,2 ]
He, Xia [1 ,2 ,3 ,4 ]
机构
[1] Nanjing Med Univ, Affiliated Canc Hosp, Jiangsu Canc Hosp, Nanjing, Jiangsu, Peoples R China
[2] Jiangsu Inst Canc Res, Nanjing, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Xuzhou, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Collaborat Innovat Ctr Canc Personalized Med, Dept Environm Genom, Jiangsu Key Lab Canc Biomarkers Prevent & Treatmen, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA-DAMAGE RESPONSE; SMALL-MOLECULE INHIBITORS; HYPOXIA-INDUCIBLE FACTORS; STRAND BREAK REPAIR; CELL-CYCLE; NEGATIVE REGULATOR; TUMOR-SUPPRESSOR; CERVICAL-CANCER; PROTEIN COMPLEX; UBIQUITIN;
D O I
10.1016/j.ijrobp.2023.12.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radiation therapy is a primary treatment for cancer, but radioresistance remains a signi fi cant challenge in improving ef fi - cacy and reducing toxicity. Accumulating evidence suggests that deubiquitinases (DUBs) play a crucial role in regulating cell sensitivity to ionizing radiation. Traditional small-molecule DUB inhibitors have demonstrated radiosensitization effects, and novel deubiquitinase-targeting chimeras (DUBTACs) provide a promising strategy for radiosensitizer development by harnessing the ubiquitin-proteasome system. This review highlights the mechanisms by which DUBs regulate radiosensitivity, including DNA damage repair, the cell cycle, cell death, and hypoxia. Progress on DUB inhibitors and DUBTACs is summarized, and their potential radiosensitization effects are discussed. Developing drugs targeting DUBs appears to be a promising alternative approach to overcoming radioresistance, warranting further research into their mechanisms. (c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/)
引用
收藏
页码:1347 / 1370
页数:24
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