miR-137 suppresses cell growth in ovarian cancer by targeting AEG-1

被引:71
作者
Guo, Jinling [1 ]
Xia, Bairong [1 ]
Meng, Fanling [1 ]
Lou, Ge [1 ]
机构
[1] Harbin Med Univ, Affiliated Tumor Hosp, Dept Gynecol, Harbin 150081, Heilongjiang Pr, Peoples R China
关键词
AEG-1; miR-137; Ovarian cancer; Cell growth; ASTROCYTE ELEVATED GENE-1; TUMOR-SUPPRESSOR; PROLIFERATION; PROGRESSION; METASTASIS; INVASION; OVEREXPRESSION; EXPRESSION; CARCINOMA; IDENTIFICATION;
D O I
10.1016/j.bbrc.2013.10.052
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
Astrocyte elevated gene-1 (AEG-1) is an oncogene overexpressed in multiple types of human cancers including ovarian cancer (OC). However, the underlying mechanism of AEG-1 up-regulation in OC is not well understood. In this study, we showed that miR-137 downregulated AEG-1 expression through interaction with its 3' untranslated region (3'UTR) and that miR-137 expression was inversely correlated with AEG-1 levels in DC specimens. Similar to the downregulation of AEG-1, overexpression of miR-137 in OC cell lines decreased in vitro cell growth, clonogenicity, and also induced G1 arrest. Importantly, miR-137 overexpression suppressed in vivo tumor growth in nude mice models. Furthermore, we found that restoring the AEG-1 (without the 3'UTR) significantly rescued miR-137-induced cell growth inhibition and cell-cycle arrest. Taken together, these findings indicate that miR-137 functions as a tumor suppressor by inhibition of AEG-1. These molecules might be targets for prevention or treatment of OC. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:357 / 363
页数:7
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