Li Kailang, Wang Haifeng, Jiang Bitao, Jin Xiaofeng
Department of Oncology and Hematology, Beilun District People's Hospital, Ningbo, China.
Department of Biochemistry and Molecular Biology, Zhejiang Key Laboratory of Pathphysiology, Medical School of Ningbo University, Ningbo, China.
Front Genet. 2024 Jul 19;15:1431564. doi: 10.3389/fgene.2024.1431564. eCollection 2024.
TRIM28 (tripartite motif protein 28) was initially believed to be a transcription inhibitor that plays an important role in DNA damage repair (DDR) and in maintaining cancer cellular stemness. As research has continued to deepen, several studies have found that TRIM28 not only has ubiquitin E3 ligase activity to promote degradation of substrates, but also can promote SUMOylation of substrates. Although TRIM28 is highly expressed in various cancer tissues and has oncogenic effects, there are still a few studies indicating that TRIM28 has certain anticancer effects. Additionally, TRIM28 is subject to complex upstream regulation. In this review, we have elaborated on the structure and regulation of TRIM28. At the same time, highlighting the functional role of TRIM28 in tumor development and emphasizing its impact on cancer treatment provides a new direction for future clinical antitumor treatment.
TRIM28(三联基序蛋白28)最初被认为是一种转录抑制剂,在DNA损伤修复(DDR)和维持癌症细胞干性方面发挥重要作用。随着研究的不断深入,多项研究发现TRIM28不仅具有泛素E3连接酶活性以促进底物降解,还能促进底物的SUMO化。尽管TRIM28在各种癌症组织中高表达并具有致癌作用,但仍有一些研究表明TRIM28具有一定的抗癌作用。此外,TRIM28受到复杂的上游调控。在本综述中,我们阐述了TRIM28的结构和调控。同时,突出TRIM28在肿瘤发生发展中的功能作用并强调其对癌症治疗的影响,为未来临床抗肿瘤治疗提供了新方向。