Suppr超能文献

二甲双胍通过抑制三结构域蛋白 37 诱导的肿瘤坏死因子受体相关因子 2 的泛素化来抑制卵巢癌细胞的增殖和侵袭。

Metformin inhibits the proliferation and invasion of ovarian cancer cells by suppressing tripartite motif-containing 37-induced tumor necrosis factor receptor-associated factor 2 ubiquitination.

机构信息

Department of Gynecology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.

Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.

出版信息

Cancer Sci. 2022 Nov;113(11):3776-3786. doi: 10.1111/cas.15524. Epub 2022 Sep 3.

Abstract

Ovarian cancer is the leading cause of death in gynecological malignancies worldwide. Our previous studies have proved that metformin inhibited the proliferation and invasion of ovarian cancer in vitro and in vivo. However, the underlying mechanisms have not been fully elucidated. Immunohistochemistry was carried out to detect the expression of tripartite motif-containing 37 (TRIM37), Ki-67, and MMP-9 in ovarian cancer and normal tissues. The influence of TRIM37 on the proliferation and invasion of ovarian cancer cells was verified by the real-time cellular analysis proliferation test, colony formation test, and Transwell assay. Western blot analysis and immunoprecipitation were used to detect the expression of the nuclear factor-κB (NF-κB) pathway and the interaction between TRIM37 and tumor necrosis factor receptor-associated factor 2 (TRAF2). Ubiquitination detection was carried out to detect the ubiquitination level of TRAF2. The present study revealed that TRIM37 expression was significantly increased in ovarian cancer tissues compared with normal control tissues, and its overexpression was closely associated with proliferation and metastasis. Metformin inhibited the NF-κB signaling pathway by downregulating TRIM37. Metformin also inhibited the ubiquitination of TRAF2 induced by TRIM37 overexpression. Metformin inhibits the proliferation and invasion of ovarian cancer cells by suppressing TRIM37-induced TRAF2 ubiquitination.

摘要

卵巢癌是全球妇科恶性肿瘤死亡的主要原因。我们之前的研究已经证明二甲双胍可以抑制卵巢癌细胞在体外和体内的增殖和侵袭。然而,其潜在机制尚未完全阐明。通过免疫组织化学检测卵巢癌和正常组织中三结构域蛋白 37(TRIM37)、Ki-67 和基质金属蛋白酶 9(MMP-9)的表达。通过实时细胞分析增殖试验、集落形成试验和 Transwell 分析验证了 TRIM37 对卵巢癌细胞增殖和侵袭的影响。通过 Western blot 分析和免疫沉淀检测核因子-κB(NF-κB)通路和 TRIM37 与肿瘤坏死因子受体相关因子 2(TRAF2)之间的相互作用。进行泛素化检测以检测 TRAF2 的泛素化水平。本研究表明,与正常对照组织相比,卵巢癌组织中 TRIM37 的表达明显增加,其过表达与增殖和转移密切相关。二甲双胍通过下调 TRIM37 抑制 NF-κB 信号通路。二甲双胍还抑制了 TRIM37 过表达诱导的 TRAF2 泛素化。二甲双胍通过抑制 TRIM37 诱导的 TRAF2 泛素化来抑制卵巢癌细胞的增殖和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b86a/9633302/ecc0384bd6ec/CAS-113-3776-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验