Department of General Surgery, Institute of Fudan-Minhang Academic Health System, Minhang Hospital, Fudan University, Shanghai.
Department of Special Ward One, Shanghai Pulmonary Hospital, Shanghai.
Eur J Histochem. 2021 Mar 10;65(1):3214. doi: 10.4081/ejh.2021.3214.
Proteins in the tripartite motif-containing protein (TRIM) family participates in carcinogenesis. However, little attention was focused on the role of TRIM6 on development of breast cancer. Expression level of TRIM6 was found to be markedly enhanced in breast cancer cells and tissues. Functional assays demonstrated that overexpression of TRIM6 promoted breast cancer progression through increase of YAP1 (Yes-associated Protein 1), while knockdown of TRIM6 suppressed in vitro breast cancer progression and in vivo tumor growth through decrease of YAP1. Co-Immunoprecipitation (co-IP) showed that TRIM6 interacted with STUB1 (stress induced phosphoprotein 1 homology and U-box containing protein 1). TRIM6 promoted ubiquitination-mediated degradation of STUB1 to promote YAP1 signaling. Overexpression of STUB1 attenuated TRIM6-induced promotion of breast cancer growth. In conclusion, TRIM6 contributed to breast cancer progression through ubiquitination-dependent proteasomal degradation of STUB1 and provocation of YAP1 pathway, providing potential therapeutic target for breast cancer.
三结构域蛋白家族中的蛋白质(TRIM)参与了致癌作用。然而,TRIM6 在乳腺癌发展中的作用尚未得到关注。研究发现,TRIM6 的表达水平在乳腺癌细胞和组织中明显升高。功能分析表明,过表达 TRIM6 通过增加 YAP1(Yes 相关蛋白 1)促进乳腺癌的进展,而敲低 TRIM6 通过降低 YAP1 抑制体外乳腺癌的进展和体内肿瘤的生长。免疫共沉淀(co-IP)表明 TRIM6 与 STUB1(应激诱导磷酸化蛋白 1 同源物和包含 U -box 的蛋白 1)相互作用。TRIM6 促进 STUB1 的泛素化介导的降解,以促进 YAP1 信号通路。过表达 STUB1 减弱了 TRIM6 诱导的乳腺癌生长促进作用。总之,TRIM6 通过 STUB1 的泛素依赖性蛋白酶体降解和引发 YAP1 途径促进乳腺癌的进展,为乳腺癌提供了潜在的治疗靶点。