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miR-372抑制卵巢癌细胞EMT、侵袭迁徙及可能机制

miR-372 inhibits EMT,invasion and migration of ovarian cancer cells and the possible mechanism

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【作者】 杨欣郭春芳陈说桑秀波宗志红赵杨

【Author】 YANG Xin;GUO Chun-fang;CHEN Shuo;SANG Xiu-bo;ZONG Zhi-hong;ZHAO Yang;Department of Gynecology of the First Hospital,China Medical University;Department of Biochemistry and Molecular Biology of Basic Medicine College,China Medical University;

【机构】 中国医科大学附属第一医院妇科中国医科大学基础医学院生物化学与分子生物学教研室

【摘要】 目的探讨miR-372在卵巢癌细胞上皮间质转化(EMT)、侵袭迁徙中的作用及相关的机制。方法利用Lipofectamine2000瞬时转染miR-372 mimics于OVCAR3和A2780细胞中,并通过RT-PCR法检测在转染前后OVCAR3和A2780细胞中miR-372的表达,Transwell及细胞划痕实验检测OVCAR3和A2780细胞的侵袭迁徙能力,蛋白印迹法检测EMT相关蛋白N-钙黏蛋白和a-SMA蛋白的表达水平。结果转染miR-372 mimics后OVCAR3和A2780细胞的miR-372相对表达量显著升高(P<0.05),细胞的侵袭迁徙能力显著降低(P<0.05);Western Blotting结果表明转染miR-372 mimics后OVCAR3和A2780细胞的EMT相关间质蛋白N-钙黏蛋白和a-SMA蛋白的表达水平显著降低。结论miR-372过表达抑制卵巢癌细胞的体外侵袭及迁徙,并通过抑制N-钙黏蛋白和a-SMA蛋白水平的表达来抑制卵巢癌细胞的EMT过程。

【Abstract】 Objective and To investigate the role and mechanism of miR-372 mimics in epithelial-mesenchymal transfected transition(EMT),and invasion by migration of ovarian the cancer cells.Methods miR-372 detected were into and OVCAR3cell A2780 were cells used Lipofectamine2000,expression of miR-372 was by RT-PCR.Transwell scratch a-SMA test to detect the invasion Western and migration ability.The expression of EMT-related proteins N-cadherin and protein was detected by blotting.Results The miR-372 expression level in OVCAR3 and A2780 cells was mimics(P<0.05).The invasion and migration ability of OVCAR3 and significantly A2780 increased were after transfection of miR-372 after transfection(P<0.05).Western blotting results showed that cells significantly decreased miR-372 mimics miR-372 overexpression reduced the expression level of EMT-related interstitial proteins N-cadherin and a-SMA EMT proteins.inhibiting Conclusion the miR-372 overexpression inhibits ovarian cancer cell invasion and migration,and inhibits via expression of N-cadherin and a-SMA protein in ovarian cancer cells.

【基金】 国家自然科学基金(81202049,81472440,81602266)
  • 【文献出处】 解剖科学进展 ,Progress of Anatomical Sciences , 编辑部邮箱 ,2017年03期
  • 【分类号】R737.31
  • 【被引频次】4
  • 【下载频次】91
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