Expression of miR-126 suppresses migration and invasion of colon cancer cells by targeting CXCR4

被引:11
作者
Zeng Li
Nan Li
Minghua Wu
Xiayu Li
Zhaohui Luo
Xiaoyan Wang
机构
[1] The Third Xiangya Hospital,Department of Gastroenterology
[2] The Central South University,Department of Gastroenterology
[3] The Xiangtan Central Hospital,The Institute of Oncology
[4] The Central South University,Department of Neurology
[5] Xiangya Hospital,undefined
[6] The Central South University,undefined
来源
Molecular and Cellular Biochemistry | 2013年 / 381卷
关键词
Colorectal cancer; miR-126; Tumor cell migration and invasion; CXCR4;
D O I
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中图分类号
学科分类号
摘要
A previous study demonstrated that miR-126 expression was significantly downregulated in highly metastatic colon cancer cells. This study was to investigate the biological function of miR-126 and its regulation of target genes in colon cancer cells. Quantitative PCR was used to detect miR-126 expression in colon cancer SW480 and SW620 cells. MTT assay was to measure the changed cell viability after miR-126 mimics transfection. Wound healing and Transwell migration and invasion assays measured capacity of tumor cell migration and invasion of SW480 and SW620 cells after miR-126 transfection. Luciferase reporter assay and Western blot were used to assess both transcriptional and expression levels of one of the miR-126 target genes (i.e., CXCR4). Levels of miR-126 expression were lower in colon cancer SW480 and SW620 cells than in the adjacent normal epithelial tissues (P < 0.05). Transfection of miR-126 mimics significantly reduced colon cancer cell viability compared to NC cells (P < 0.05). The wound healing and Transwell migration and invasion assays showed that miR-126 mimics inhibited SW480 and SW620 cell migration and invasion capacity. Bioinformatics predicted that CXCR4 is one of the miR-126 target genes. Indeed, luciferase reporter assay and Western blot confirmed that CXCR4 is a miR-126 target gene. Expression of miR-126 inhibited colon cancer cell viability and reduced tumor cell migration and invasion capacity by its negative regulation of CXCR4 expression.
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页码:233 / 242
页数:9
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共 140 条
[11]  
Pancione M(2008)The noncoding RNA, miR-126, suppresses the growth of neoplastic cells by targeting phosphatidylinositol 3-kinase signaling and is frequently lost in colon cancers Genes Chromosom Cancer 47 939-946
[12]  
Forte N(2011)Down-regulation of miR-126 expression in colorectal cancer and its clinical significance Med Oncol 28 1054-1057
[13]  
Fucci A(2008)Endogenous human microRNAs that suppress breast cancer metastasis Nature 451 147-152
[14]  
Sabatino L(2011)A microRNA regulon that mediates endothelial recruitment and metastasis by cancer cells Nature 481 190-194
[15]  
Febbraro A(2008)MicroRNA-126 inhibits invasion in non-small cell lung carcinoma cell lines Biochem Biophys Res Commun 373 607-612
[16]  
Di Blasi A(2010)miR-126 functions as a tumour suppressor in human gastric cancer Cancer Lett 298 50-63
[17]  
Daniele B(2008)miR-126 regulates angiogenic signaling and vascular integrity Dev Cell 15 272-284
[18]  
Parente D(2002)Identification of tissue-specific microRNAs from mouse Curr Biol 12 735-739
[19]  
Colantuoni V(2007)A mammalian microRNA expression atlas based on small RNA library sequencing Cell 129 1401-1414
[20]  
Roger L(2000)Stromal-derived factor 1 and thrombopoietin regulate distinct aspects of human megakaryopoiesis Blood 96 4142-4151