Yamada Yuta, Kimura Naoki, Maki Kazuki, Hakozaki Yuji, Urabe Fumihiko, Kimura Shoji, Fujimura Tetsuya, Inoue Satoshi, Kume Haruki
Department of Urology, Graduate School of Medicine, The University of Tokyo, Bunkyo-Ku, Tokyo 113-8655, Japan.
Department of Urology, The Jikei University Daisan Hospital, Komae-Shi 201-8601, Tokyo, Japan.
Cancers (Basel). 2025 Jul 16;17(14):2367. doi: 10.3390/cancers17142367.
We aimed to investigate the roles of tripartite motif (TRIM) proteins in urological cancers. : A systematic review was conducted to investigate the oncological role of tripartite motif proteins in urological cancers. : A total of 84 articles were identified for the final analysis (26 articles on kidney cancers, 19 on bladder cancers, 37 on prostate cancers, and 1 on testicular cancers). In total, 27 TRIM family proteins were involved in kidney cancer, of which 9 were associated with tumor-promoting findings (TRIM24, TRIM27, TRIM37, TRIM44, TRIM46, TRIM47, TRIM59, TRIM63, and TRIM65) and of which 9 TRIM proteins were tumor-suppressive (TRIM2, TRIM7, TRIM8, TRIM13, TRIM21, TRIM26, TRIM28, TRIM33, and TRIM58). Fourteen TRIM family proteins were associated with bladder cancer (tumor-promoting: TRIM9, TRIM25, TRIM26, TRIM28, TRIM29, TRIM59, TRIM65, and TRIM66; tumor-suppressive: TRIM19 and TRIM38). Ten TRIM family proteins were associated with prostate cancer (tumor-promoting: TRIM11, TRIM24, TRIM28, TRIM33, TRIM44, TRIM59, TRIM63, TRIM66, and TRIM68; tumor-suppressive: TRIM32 and TRIM36). Twenty-eight TRIM family proteins were identified to be associated with prostate cancer (tumor-promoting: TRIM11, TRIM24, TRIM28, TRIM33, TRIM44, TRIM59, TRIM63, TRIM66, and TRIM68; tumor-suppressive: TRIM32 and TRIM36). TRIM proteins regulate urological cancers by ubiquitination or modulation of oncologic pathways. : This review identifies TRIM proteins that are involved in urological cancers. Some of these proteins have the potential to be the therapeutic target.
我们旨在研究三联基序(TRIM)蛋白在泌尿系统癌症中的作用。:进行了一项系统综述,以研究三联基序蛋白在泌尿系统癌症中的肿瘤学作用。:共确定84篇文章用于最终分析(26篇关于肾癌,19篇关于膀胱癌,37篇关于前列腺癌,1篇关于睾丸癌)。总共有27种TRIM家族蛋白参与肾癌,其中9种与促进肿瘤的结果相关(TRIM24、TRIM27、TRIM37、TRIM44、TRIM46、TRIM47、TRIM59、TRIM63和TRIM65),9种TRIM蛋白具有肿瘤抑制作用(TRIM2、TRIM7、TRIM8、TRIM13、TRIM21、TRIM26、TRIM28、TRIM33和TRIM58)。14种TRIM家族蛋白与膀胱癌相关(促进肿瘤:TRIM9、TRIM25、TRIM26、TRIM28、TRIM29、TRIM59、TRIM65和TRIM66;肿瘤抑制:TRIM19和TRIM38)。10种TRIM家族蛋白与前列腺癌相关(促进肿瘤:TRIM11、TRIM24、TRIM28、TRIM33、TRIM44、TRIM59、TRIM63、TRIM66和TRIM68;肿瘤抑制:TRIM32和TRIM36)。28种TRIM家族蛋白被确定与前列腺癌相关(促进肿瘤:TRIM11、TRIM24、TRIM28、TRIM33、TRIM44、TRIM59、TRIM63、TRIM66和TRIM68;肿瘤抑制:TRIM32和TRIM36)。TRIM蛋白通过泛素化或调节肿瘤途径来调控泌尿系统癌症。:本综述确定了参与泌尿系统癌症的TRIM蛋白。其中一些蛋白有可能成为治疗靶点。