吉林大学学报(医学版) ›› 2018, Vol. 44 ›› Issue (01): 106-110.doi: 10.13481/j.1671-587x.20180120

• 基础研究 • 上一篇    下一篇

miR-200c对三阴性乳腺癌上皮间质转化的抑制作用及其机制

马啸天1, 岳小欣2, 荣守华1, 张玉超1, 田远1, 石瑛1, 李君芳3, 贾莉婷1   

  1. 1. 郑州大学第三附属医院检验科, 河南 郑州 450052;
    2. 河南省高等医学专科学校药学系, 河南 郑州 451191;
    3. 河南省漯河市中心医院, 河南 漯河 462000
  • 收稿日期:2017-08-14 出版日期:2018-01-28 发布日期:2018-01-24
  • 通讯作者: 贾莉婷,教授,硕士研究生导师(Tel:0371-66903509,E-mail:jialt@163.com) E-mail:jialt@163.com
  • 作者简介:马啸天(1992-),男,河南省郑州市人,在读医学硕士,主要从事临床免疫学方面的研究。
  • 基金资助:
    河南省科技厅医学科技攻关计划重点项目资助课题(201402021)

Inhibitory effect of miR-200c on epithelial-mesenchymal transiton in triple negative breast cancer and its mechanism

MA Xiaotian1, YUE Xiaoxin2, RONG Shouhua1, ZHANG Yuchao1, TIAN Yuan1, SHI Ying1, LI Junfang3, JIA Liting1   

  1. 1. Department of Clinical Laboratory, Third Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, China;
    2. Department of Pharmacy, Henan Medical College, Zhengzhou 451191, China;
    3. Luohe Central Hospital, Henan Province, Luohe 462000, China
  • Received:2017-08-14 Online:2018-01-28 Published:2018-01-24

摘要: 目的:研究miR-200c对乳腺癌MDA-MB-231细胞和BT-549细胞迁移能力及增殖能力的影响,阐明miR-200c抑制三阴性乳腺癌上皮间质转化(EMT)的相关机制。方法:选取三阴性乳腺癌细胞系MDA-MB-231和BT-549,对其进行瞬时转染,分为空白对照组、阴性对照组(转染negative control/Lipo2000)、试剂对照组(转染Lipo2000)和实验组(转染miR-200c mimic/Lipo2000);利用RT-PCR和Western blotting法分别检测vimentin及β-catenin mRNA和蛋白表达水平;采用CCK8实验和划痕实验分别检测细胞增殖能力和迁移能力。结果:RT-PCR法和Westernblotting法检测,实验组细胞中vimentin和β-catenin mRNA和蛋白表达水平降低,与空白对照组、阴性对照组和试剂对照组比较差异均有统计学意义(P<0.05)。CCK8法检测,实验组细胞增殖低于阴性对照组和试剂对照组(P<0.05)。划痕实验,实验组细胞划痕宽度恢复率低于阴性对照组和试剂对照组(P<0.05)。结论:miR-200c通过调节MDA-MB-231和BT-549中β-catenin、vimentin的mRNA和蛋白表达量、降低细胞的迁移和增殖能力,进而抑制三阴性乳腺癌EMT。

关键词: β-链接蛋白, 三阴性乳腺癌, 乳腺肿瘤, 波形蛋白, 上皮间质转化, miR-200c

Abstract: Objective: To study the effect of miR-200c on the migration and proliferation abilities of breast cancer MDA-MB-231 and BT-549 cells,and to clarify the mechanism of miR-200c in inhibiting the epithelial-mesenchymal transiton (EMT) of triple negative breast cancer. Methods: The human triple negative breast cancer cell lines (MDA-MB-231 and BT-549) were chosen in this study.The cells were transiently transfected with miR-200c mimics and Lipo2000(experimental group),miR-200c negative control and Lipo2000(negative control group),and Lipo2000 alone (reagent control group); at the same time, blank control group was set up.The expression levels of vimentin and β-catenin mRNA and protein were detected by RT-PCR and Western blotting method.The proliferation rates and migration abilities of MDA-MB-231 cells and BT-549 cells after transfection of miR-200c were analyzed by CCK8 assay and wound healing assay. Results: The RT-PCR and Western blotting showed that the expression levels of vimentin and β-catenin mRNA and proteins in experimental group were decreased,and the differences were statistically significant compared with blank control group, negative control group and reagent control group(P<0.05).The CCK8 results showed that the proliferation rates of the cells in experimental group were lower than those in negative control group and reagent control group(P<0.05).The wound healing assay results showed that the recovery rate of scratch width in experimental group was lower than those in negative control group and reagent control group (P<0.05). Conclusion: miR-200c might inhibit EMT in triple negative breast cancer by regulating the expressions of β-catenin and vimentin mRNA and proteins in MDA-MB-231 and BT-549 cells and decreasing the abilities of migration and proliferation of triple negative breast cancer cells.

Key words: β-catenin, epithelial-mesenchymal transiton, triple negative breast cancer, vimentin, breast neoplasms, miR-200c

中图分类号: 

  • R737.9