Wang Chengcai, Jiang Huamao
Department of Urinary Surgery, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Rejuvenation Res. 2025 Jun;28(3):113-124. doi: 10.1089/rej.2024.0061. Epub 2024 Dec 23.
As a typical E3 ligase, tripartite motif-containing 65 (TRIM65), is implicated in the modulation of biological processes, such as metastasis, proliferation, and apoptosis. However, the function of TRIM65 in prostate cancer (PCa) and its potential mechanism have not yet been excavated. In this work, we affirmed Tripartite motif-containing protein 65 (TRIM65) as a new oncogene in PCa, which accelerated PCa cell proliferation and impeded cell ferroptosis. , depletion of TRIM65 inhibited PCa tumorigenesis and metastasis. Mechanically, our findings uncovered that TRIM65 enhances NKD inhibitor of WNT signaling pathway 2 (NKD2) degradation via the ubiquitin-proteasome signaling. TRIM65 facilitated proliferation and restricted ferroptosis via downregulating NKD2 levels. Moreover, TRIM65 activated the wingless-integrated/β-catenin pathway in PCa cells via inhibiting NKD2. Taken together, these data uncovered that TRIM65 controls PCa proliferation, and ferroptosis and regulates the Wnt/β-catenin signaling via directly targeting NKD2 for ubiquitination degradation. Our study provides insights into the multifaceted regulatory role of TRIM65 in the development of PCa, laying the foundation for exploring new therapeutic approaches.
作为一种典型的E3连接酶,含三联基序蛋白65(TRIM65)参与调节转移、增殖和凋亡等生物学过程。然而,TRIM65在前列腺癌(PCa)中的功能及其潜在机制尚未被挖掘。在这项研究中,我们证实含三联基序蛋白65(TRIM65)是PCa中的一种新致癌基因,它加速PCa细胞增殖并抑制细胞铁死亡。此外,TRIM65的缺失抑制PCa肿瘤发生和转移。从机制上来说,我们的研究结果发现TRIM65通过泛素-蛋白酶体信号增强WNT信号通路的NKD抑制因子2(NKD2)的降解。TRIM65通过下调NKD2水平促进增殖并限制铁死亡。此外,TRIM65通过抑制NKD2激活PCa细胞中的无翅型MMTV整合位点家族/β-连环蛋白信号通路。综上所述,这些数据表明TRIM65通过直接靶向NKD2进行泛素化降解来控制PCa的增殖和铁死亡,并调节Wnt/β-连环蛋白信号通路。我们的研究为TRIM65在PCa发展中的多方面调节作用提供了见解,为探索新的治疗方法奠定了基础。