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miR-203在舌癌组织中的表达及其对Tca8113细胞活力和侵袭的影响

郑红 张文玲 林波 张赛男 刘瑞敏 薛鹏

中国病理生理杂志2016,Vol.32Issue(10):1896-1899,1904,5.
中国病理生理杂志2016,Vol.32Issue(10):1896-1899,1904,5.DOI:10.3969/j.issn.1000-4718.2016.10.026

miR-203在舌癌组织中的表达及其对Tca8113细胞活力和侵袭的影响

Expression of miR-203 in human tongue carcinoma tissues and its in-fluence on viability and invasion ability of Tca8113 cells

郑红 1张文玲 2林波 1张赛男 3刘瑞敏 3薛鹏3

作者信息

  • 1. 河南大学医学院病理生理学教研室,河南开封475004
  • 2. 河南大学淮河临床学院口腔科,河南开封475004
  • 3. 河南大学医学院免疫学教研室,河南开封475004
  • 折叠

摘要

Abstract

[ ABSTRACT] AIM:To study the expression of miR-203 in tongue carcinoma tissues and the effect of miR-203 over-expression on the viability and invasion ability of Tca 8113 cells.METHODS:Twenty-eight pairs of tongue carcinoma tissues and adjacent nontumor tissues were collected , and the clinicopathological characters were analyzed .miR-203 was detected in the tongue tissues of 28 patients with tongue carcinoma by real-time PCR.miR-203 mimics and scramble were transfected into Tca8113 cells by Lipofectamine 2000.The expression of miR-203 was detected in Tca8113, Tca8113-miR-203 mimics and Tca8113-scramble cells by RT-qPCR.The cell viability was measured by CCK-8 assay.The cell invasion ability was determined by Transwell chamber invasion experiment .RESULTS:miR-203 expression was significantly down-regulated in the tongue carcinoma tissues compared with those in the adjacent nontumor tissues .The expression of miR-203 was associated with TNM stage and lymph node metastasis .Up-regulation of miR-203 inhibited the viability and invasion a-bility of Tca8113 cells.CONCLUSION:miR-203 suppresses the growth and invasion of tongue carcinoma cells .miR-203 may be a potential therapeutic target for treating human tongue cancer .

关键词

miR-203/舌癌/细胞活力/细胞侵袭

Key words

miR-203/Tongue carcinoma/Cell viability/Cell invasion

分类

医药卫生

引用本文复制引用

郑红,张文玲,林波,张赛男,刘瑞敏,薛鹏..miR-203在舌癌组织中的表达及其对Tca8113细胞活力和侵袭的影响[J].中国病理生理杂志,2016,32(10):1896-1899,1904,5.

基金项目

开封市科技发展计划项目(No.1503112);河南大学科研基金重点项目 ()

中国病理生理杂志

OA北大核心CSCDCSTPCD

1000-4718

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