文章摘要

MicroRNA-197调控上皮-间充质转化对乳腺癌侵袭和迁移的影响

作者: 1沈庆林, 1宋启斌, 1章必成, 1姚颐, 1彭敏
1 武汉大学人民医院肿瘤中心,武汉 430060
通讯: 宋启斌 Email: qibinsong@163.com
DOI: 10.3978/j.issn.2095-6959. 2018.12.001 
基金: 国家自然科学基金(81472748)。

摘要

目的:探讨微小RNA-197(miR-197)抑制乳腺癌细胞迁移和侵袭的能力,以及阻断上皮-间充质转化(epithelial-mesenchymal transition,EMT)过程的机制。方法:构建miR-197过表达载体(miR-197 mimics),分别转染MDA-MB-231和MCF-7细胞,并设对照组;Real-time PCR分别检测以上各组细胞miR-197的表达水平变化;利用Transwell实验和划痕实验对乳腺癌细胞侵袭和迁移能力进行检测;Western印迹法检测过表达miR-197后对EMT相关标志物E-cadherin,snail和vimentin表达的影响。结果:MiR-197可以抑制乳腺癌细胞MDA-MB-231和MCF-7的迁移和侵袭能力;转染miR-197 mimics后,E-cadherin表达降低,snail和vimentin表达增加。结论:MiR-197有可能作为乳腺癌临床治疗的新靶点。
关键词: 乳腺癌;微小RNA-197;上皮-间充质转化;侵袭;迁移

Effects of microRNA-197 regulating epithelial mesenchymal transition on invasion and migration in breast cancer

Authors: 1SHEN Qinglin, 1SONG Qibin, 1ZHANG Bicheng, 1YAO Yi, 1PENG Min
1 Cancer Center, Renmin Hospital, Wuhan University, Wuhan 430060, China

CorrespondingAuthor: SONG Qibin Email: qibinsong@163.com

DOI: 10.3978/j.issn.2095-6959. 2018.12.001 

Foundation: This study was supported by the National Natural Science Foundation of China (81472748).

Abstract

Objective: To investigate the ability of microRNA-197 (miR-197) to inhibit the migration and invasion of breast cancer cells and the mechanism of blocking the process of epithelial-mesenchymal transition (EMT). Methods: The miR-197 mimics vector was constructed, and transfected into MDA-MB-231 and MCF-7 cell, the control group were transfected with empty vectors. The expression of miR-197 was detected by real-time PCR. The transwell system and the wound healing were used to assess the invasion and migration ability of breast cancer cell line MDA-MB-231 and MCF-7. Western blot was used to assay the expression of E-cadherin, Snail and Vimentin, which were the markers of EMT. Results: MiR-197 inhibited the migration and invasion of breast cancer cells MDA-MB-231 and MCF-7. Transfection of miR-197 mimics reduced the expression of E-cadherin and increased the protein expression of snail and vimentin. Conclusion: MiR-197 may be a new target for clinical treatment of breast cancer.
Keywords: breast cancer; microRNA-197; epithelial-mesenchymal transition; invasion; migration

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