Suppr超能文献

miR-375 通过阻断 JAK2/STAT3 信号通路抑制乳腺癌干细胞的干性。

MiR-375 inhibits the stemness of breast cancer cells by blocking the JAK2/STAT3 signaling.

机构信息

School of Life Science and Technology, Jiangsu Key Laboratory of Carcinogenesis and Intervention, China Pharmaceutical University, Longmian Road 639, Nanjing, 211198, PR China.

Department of Pharmacy, The Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, 127 Dongming Road, Zhengzhou, 450003, PR China.

出版信息

Eur J Pharmacol. 2020 Oct 5;884:173359. doi: 10.1016/j.ejphar.2020.173359. Epub 2020 Jul 30.

Abstract

The relapse of breast cancer could be due to the existence of breast cancer stem cells (BCSCs). Other and our researches have indicated the suppressive roles of miR-375 in various tumors, however, its roles in breast cancer stemness remain confusing. Here, we constructed breast cancer cells with miR-375 stable overexpression via lentivirus infection. Flow cytometry, Western blot, mammosphere formation, cell colony formation and CCK8 as well as in vivo assays were performed to identify the role of miR-375 in the stemness of breast cancer cells. Luciferase reporter, RNA-Fluorescence in situ hybridization (RNA-FISH) and RNA-binding protein immunoprecipitation (RIP) assays were utilized to elucidate the mechanism whereby miR-375 exerts its effects. It was found that miR-375 not only reduced the stemness, but also decreased adriamycin resistance of breast cancer cells. These results were characterized by the decrease of BCSC rate, mammosphere-forming and tumor-initiating ability, and IC value of adriamycin, and weakened by JAK2 re-expression. This work indicates that miR-375 suppresses the stemness of breast cancer cells through targeting JAK2.

摘要

乳腺癌的复发可能是由于乳腺癌干细胞(BCSCs)的存在。其他和我们的研究表明,miR-375 在各种肿瘤中具有抑制作用,然而,其在乳腺癌干细胞特性中的作用仍存在混淆。在这里,我们通过慢病毒感染构建了 miR-375 稳定过表达的乳腺癌细胞。通过流式细胞术、Western blot、乳腺球形成、细胞集落形成和 CCK8 以及体内实验来鉴定 miR-375 在乳腺癌细胞干性中的作用。荧光素酶报告、RNA-荧光原位杂交(RNA-FISH)和 RNA 结合蛋白免疫沉淀(RIP)实验用于阐明 miR-375 发挥作用的机制。结果发现,miR-375 不仅降低了乳腺癌细胞的干性,还降低了阿霉素耐药性。这些结果的特征是 BCSC 率、乳腺球形成和肿瘤起始能力以及阿霉素的 IC 值降低,而 JAK2 的重新表达则减弱了这些结果。这项工作表明,miR-375 通过靶向 JAK2 抑制乳腺癌干细胞的干性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验