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MicroRNA-200c在结直肠癌中的表达及对侵袭和转移的影响

叶伟标 徐咏强 李妤玲 卢碧燕 杨湘玲 刘焕亮 李仲均

中山大学学报(医学科学版)2018,Vol.39Issue(3):335-340,6.
中山大学学报(医学科学版)2018,Vol.39Issue(3):335-340,6.

MicroRNA-200c在结直肠癌中的表达及对侵袭和转移的影响

Expression of MicroRNA-200c in Colorectal Carcinomas and Its Role on Tumor Cell Migration and Invasion

叶伟标 1徐咏强 2李妤玲 1卢碧燕 1杨湘玲 2刘焕亮 3李仲均2

作者信息

  • 1. 南方医科大学附属东莞人民医院,广东东莞523059
  • 2. 广东省结直肠盆底疾病研究重点实验室,广东广州510655
  • 3. 中山大学附属第六医院,广东广州510655
  • 折叠

摘要

Abstract

[Objective] To investigate the expression of microRNA-200c (miR-200c) in colorectal carcinomas (CRC),and analyze its role on tumor cell migration and invasion.[Methods] The expression levels of miR-200c in CRC tissues and adjacent normal mucosa were assessed by real-time quantitative RT-PCR (qRT-PCR).miR-200c mimics were transiently transfected into human colorectal cancer cells,and their roles on cell migration and invasion were analyzed by Transwell assay.Cell proliferation was measured using the Cell Counting kit-8.The expression levels of epithelial and mesenchymal markers as well as related transcription factor ZEB1 were detected by Western blotting.[Results] Lower miR-200c expression was found in primary CRC tissues with lymph node metastasis compared to those without lymph node metastasis and adjacent normal mucosa.Transfection of miR-200c mimics suppressed proliferation,and reduced invasion and migration in SW620 cells.Furthermore,up-regulation of miR-200c inhibited ZEB1,and resulted in increased E-cadherin and reduced Vimentin gene expression.[Conclusion] miR-200c was associated with invasive and metastatic behavior of CRC.These effects may be mediated through regulation of epithelial-mesenchymal transition.

关键词

microRNA-200c/结直肠癌/肿瘤转移/上皮间质转化

Key words

microRNA-200c (miR-200c)/colorectal carcinomas/tumor metastasis/epithelial-mesenchymal transition

分类

医药卫生

引用本文复制引用

叶伟标,徐咏强,李妤玲,卢碧燕,杨湘玲,刘焕亮,李仲均..MicroRNA-200c在结直肠癌中的表达及对侵袭和转移的影响[J].中山大学学报(医学科学版),2018,39(3):335-340,6.

基金项目

国家自然科学基金青年科学基金(81702399) (81702399)

广东省医学科研基金(C2017034) (C2017034)

中山大学学报(医学科学版)

OA北大核心CSCDCSTPCD

1672-3554

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