miR-663a inhibits hepatocellular carcinoma cell proliferation and invasion by targeting HMGA2

被引:45
|
作者
Huang, Weizhen [1 ]
Li, Jun [1 ]
Guo, Xiaohong [1 ]
Zhao, Yingchu [2 ]
Yuan, Xia [1 ]
机构
[1] Huizhou Municipal Cent Hosp Guangdong Prov, Dept Med Oncol, 41 North Eling Rd, Huizhou 516000, Guangdong, Peoples R China
[2] Univ Missouri, Dept Biochem, 117 Schweitzer Hall, Columbia, MO 65211 USA
关键词
Hepatocellular carcinoma; miR-663a; HMGA2; NONCODING RNA; MESENCHYMAL TRANSITION; BETA-CATENIN; TUMOR-GROWTH; PROMOTES; METASTASIS; EXPRESSION; OVEREXPRESSION; BIOMARKERS; MICRORNAS;
D O I
10.1016/j.biopha.2016.04.034
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hepatocellular carcinoma (HCC) is a highly aggressive solid malignancy throughout the world. Dysregulation of miRNAs play essential roles in HCC progression via aberrant regulation of cell proliferation, apoptosis, as well as metastasis. miR-663a is a poorly investigated miRNA. Whether miR-663a regulates HCC development remains unknown. The aim of the study was to explore the role of miR-663a in HCC development. To determine the expression level of miR-663a in HCC, we analyzed the data from GSE21362 and TCGA. The results showed that miR-663a was significantly down-regulated in HCC tissue compared with adjacent non-tumor tissue. Gain of function and loss of function assays revealed that miR-663a distinctly inhibited cell proliferation, migration and invasion. Mechanistic investigations demonstrated that miR-663a modulated cell functions through targeting and suppressing high mobility group A2 (HMGA2). In addition, overexpression of HMGA2 remarkably attenuated the tumor repressive effect of miR-663a. Taken together, miR-663a inhibits HCC cell proliferation and motility by targeting HMGA2. (C) 2016 Published by Elsevier Masson SAS.
引用
收藏
页码:431 / 438
页数:8
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