MicroRNA-221 promotes colorectal cancer cell invasion and metastasis by targeting RECK

被引:90
|
作者
Qin, Jun [1 ]
Luo, Meng [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Gen Surg, Renji Hosp, Shanghai 200127, Peoples R China
关键词
miR-221; RECK; Metastasis; Colorectal cancer; CYSTEINE-RICH PROTEIN; PROGNOSTIC MARKER; TUMOR-SUPPRESSOR; EXPRESSION; MIR-221; INVASIVENESS; CDKN1C/P57; REGULATOR; GROWTH;
D O I
10.1016/j.febslet.2013.11.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) have recently emerged as regulators of metastasis. We provide insight into the behavior of miR-221 in colorectal cancer (CRC) metastasis by showing that miR-221 is significantly upregulated in metastatic CRC cell lines and tissues. miR-221 overexpression enhances, whereas miR-221 depletion reduces CRC cell migration and invasion in vitro and metastasis in vivo. We identify RECK as a direct target of miR-221, reveal its expression to be inversely correlated with miR-221 in CRC samples and show that its re-introduction reverses miR-221-induced CRC invasiveness. Collectively, miR-221 is an oncogenic miRNA which may regulate CRC migration and invasion through targeting RECK. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:99 / 104
页数:6
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