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UCHL3:DNA损伤修复和肿瘤进展中的关键去泛素化酶。

UCHL3: a crucial deubiquitinase in DNA damage repair and tumor progression.

作者信息

Liu Jiahao, Hu Shulu, Xiao Junqi, Zhou Jumei

机构信息

The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University/Hunan Cancer Hospital, Changsha, 410013, China.

出版信息

Cancer Cell Int. 2025 Jul 21;25(1):276. doi: 10.1186/s12935-025-03884-x.


DOI:10.1186/s12935-025-03884-x
PMID:40691601
Abstract

Ubiquitin carboxyl terminal hydrolase L3 (UCHL3) is a deubiquitinase belonging to UCH protease family. Previous studies have demonstrated that abnormal expression of UCHL3 is correlated with the development of human diseases, especially in tumors. Notably, UCHL3 exhibits contradictory biological functions across different cancer types. Initial studies identified UCHL3 as a tumor suppressor in prostate cancer. However, emerging evidence suggests that UCHL3 serves as an oncogene in other cancers. Several UCHL3 inhibitors have shown a promising anti-tumor effect in vitro and in vivo. UCHL3 has also been linked to DNA damage repair, which is essential for genome stability. Overexpression of UCHL3 enhances DNA damage repair induced resistance to chemotherapy or radiotherapy in certain tumor types. This review aims to summarize the promoting role of UCHL3 in DNA damage repair and its dual, paradoxical roles in tumor progression, along with the associated mechanisms, and to provide insights into the use of UCHL3 as a therapeutic target for overcoming DNA damage repair-mediated resistance to chemotherapy and radiotherapy, as well as for treating tumors.

摘要

泛素羧基末端水解酶L3(UCHL3)是一种属于UCH蛋白酶家族的去泛素化酶。先前的研究表明,UCHL3的异常表达与人类疾病的发生发展相关,尤其是在肿瘤中。值得注意的是,UCHL3在不同癌症类型中表现出相互矛盾的生物学功能。最初的研究将UCHL3鉴定为前列腺癌中的肿瘤抑制因子。然而,新出现的证据表明,UCHL3在其他癌症中作为癌基因发挥作用。几种UCHL3抑制剂在体外和体内均显示出有前景的抗肿瘤作用。UCHL3还与DNA损伤修复有关,这对基因组稳定性至关重要。在某些肿瘤类型中,UCHL3的过表达增强了DNA损伤修复诱导的对化疗或放疗的抗性。本综述旨在总结UCHL3在DNA损伤修复中的促进作用及其在肿瘤进展中的双重、矛盾作用以及相关机制,并为将UCHL3用作克服DNA损伤修复介导的化疗和放疗抗性以及治疗肿瘤的治疗靶点提供见解。

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本文引用的文献

[1]
TDP1 phosphorylation by CDK1 in mitosis promotes MUS81-dependent repair of trapped Top1-DNA covalent complexes.

EMBO J. 2024-9

[2]
Potential roles of UCH family deubiquitinases in tumorigenesis and chemical inhibitors developed against them.

Am J Cancer Res. 2024-6-15

[3]
YBX1 promotes homologous recombination and resistance to platinum-induced stress in ovarian cancer by recognizing m5C modification.

Cancer Lett. 2024-8-10

[4]
High expression of PPP1CC promotes NHEJ-mediated DNA repair leading to radioresistance and poor prognosis in nasopharyngeal carcinoma.

Cell Death Differ. 2024-5

[5]
Circ Drives Gastric Cancer Progression through Suppressing Degradation via Interacting with UCHL3.

Int J Mol Sci. 2024-2-29

[6]
Ubiquitin Carboxyl-Terminal Hydrolase L1 and Its Role in Parkinson's Disease.

Int J Mol Sci. 2024-1-21

[7]
UCHL-3 as a potential biomarker of ovarian cancer.

Gynecol Oncol. 2024-3

[8]
Enzymatic Processing of DNA-Protein Crosslinks.

Genes (Basel). 2024-1-10

[9]
Unveiling the mechanistic link between extracellular amyloid fibrils, mechano-signaling and YAP activation in cancer.

Cell Death Dis. 2024-1-11

[10]
induced UCHL3 to promote colon cancer progression.

Am J Cancer Res. 2023-12-15

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