论著·基础研究

下调miR-27a表达对三阴乳腺癌细胞增殖、迁移和侵袭的影响

  • 程 龙1 ,
  • 徐五琴2 ,
  • 张 鹏1 ,
  • 黄建军1 ,
  • 李小宁1
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  • 1. 皖南医学院弋矶山医院检验科,芜湖 241001;2. 皖南医学院弋矶山医院病理科,芜湖 241001
程 龙(1985—),男,主管检验师,硕士;电子信箱:chenglong@wnmc.edu.cn。

网络出版日期: 2020-03-20

基金资助

重大疾病非编码RNA转化研究安徽普通高校重点实验室(皖南医学院)开放课题(RNA201904);活性生物大分子研究安徽省重点实验室自主研究项目(LAB201809)。

Effect of miR-27a down-regulation on proliferation, migration and invasion in triple-negative breast cancer cells

  • CHENG Long ,
  • XU Wu-qin ,
  • ZHANG Peng ,
  • HUANG Jian-jun ,
  • LI Xiao-ning
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  • 1. Clinical Laboratory, Yijishan Hospital of Wannan Medical College, Wuhu 241001, China; 2. Department of Pathology, Yijishan Hospital of Wannan Medical College , Wuhu 241001, China

Online published: 2020-03-20

Supported by

Open Project of Key Laboratory for Non-coding RNA Transformation Research of Anhui Higher Education Institution (Wannan Medical College) (RNA201904); Anhui Province Key Laboratory of Active Biological Macro-molecules Research (LAB201809).

摘要

目的·探讨下调miR-27a表达对三阴乳腺癌(triple-negative breast cancer,TNBC)细胞系MDA-MB-453增殖、迁移和侵袭的影响。方法·采用实时荧光定量PCR方法检测68例TNBC患者癌组织及癌旁组织标本的miR-27a表达,分析miR-27a表达与患者临床特征的关系;并检测TNBC细胞系MDA-MB-453及正常乳腺上皮细胞MCF-10A中miR-27a表达的差异。在MDA-MB-453细胞中转染miR-27a抑制物(miR-27a inhibitor),采用CCK-8实验、Transwell小室法检测miR-27a inhibitor转染组(miR-27a inhibitor组)与miR-27a阴性对照片段转染组(NC组)TNBC细胞增殖、迁移和侵袭能力的差异。蛋白质印迹法检测转染miR-27a抑制物对MDA-MB-453细胞泛素连接酶FBW7(F-box and WD repeat domain-containing 7)及Egl 9同源物2(Egl nine homolog 2,EGLN2)蛋白表达的影响。结果·TNBC组织中miR-27a表达明显高于癌旁组织,差异有统计学意义(PPPPPP结论·miR-27a在TNBC组织及细胞株中表达升高;下调miR-27a表达可以抑制TNBC细胞MDA-MB-453的增殖、迁移和侵袭能力,这可能与其下调后FBW7蛋白表达增加、EGLN2蛋白表达减少有关。

本文引用格式

程 龙1 , 徐五琴2 , 张 鹏1 , 黄建军1 , 李小宁1 . 下调miR-27a表达对三阴乳腺癌细胞增殖、迁移和侵袭的影响[J]. 上海交通大学学报(医学版), 2020 , 40(2) : 188 . DOI: 10.3969/j.issn.1674-8115.2020.02.007

Abstract

Objective · To investigate the effect of miR-27a down-regulation on proliferation, migration and invasion in triple-negative breast cancer (TNBC) cell line MDA-MB-453. Methods · Sixty-eight pairs of breast cancer tissues and para-carcinoma tissues the TNBC cancer patients were harvested for the study. The differential of miR-27a in the collected tissues, MDA-MB-453 cell line and normal breast epithetial cell line MCF-10A were detectedquantitative real-time PCR (qPCR). The relationship between miR-27a and the clinical characteristics of TNBC patients was analyzed. miR-27a inhibitor was transfected into MDA-MB-453 cell line. CCK-8 assay and Transwell chamber test were used to detect the difference in proliferation, migration and invasion of MDA-MB-453 cells between miR-27a inhibitor group and negative control group (NC group). The levels of F-box and WD repeat domain-containing 7 (FBW7) and Egl nine homolog 2 (EGLN2) protein were examinedWestern blotting. Results · The of miR-27a in TNBC tissues was significantly higher than that in para-carcinoma tissues (PPPPPPPConclusion · The of miR-27a in TNBC tissues and TNBC cell line increases. Down-regulation of miR-27a can inhibit the proliferation, migration and invasion of MDA-MB-453 cells, which may be through increasing FBW7 and decreasing EGLN2 .
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