Growth inhibitory effects of three miR-129 family members on gastric cancer

被引:103
作者
Yu, Xiuchong
Song, Haojun
Xia, Tian
Han, Shuang
Xiao, Bingxiu
Luo, Lin
Xi, Yang
Guo, Junming [1 ]
机构
[1] Ningbo Univ, Dept Biochem & Mol Biol, Sch Med, Ningbo 315211, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA-129; Gastric cancer; Tumor suppressor; Cell cycle; Cell growth; EPITHELIAL-MESENCHYMAL TRANSITION; TRANSCRIPTION FACTOR 4; MICRORNA EXPRESSION; CELL-PROLIFERATION; EPIGENETIC REGULATION; SOX4; EXPRESSION; SMALL RNA; IDENTIFICATION; METASTASIS; REPRESSION;
D O I
10.1016/j.gene.2013.09.048
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reduced expression of microRNA-129 (miR-129) has been reported in several types of tumor cell lines as well as in primary tumor tissues. However, little is known about how miR-129 affects cell proliferation in gastric cancer. Here, we show that all miR-129 family members, miR-129-1-3p, miR-129-2-3p, and miR-129-5p, are down-regulated in gastric cancer cell lines compared with normal gastric epithelial cells. Furthermore, using the real-time cell analyzer assay to observe the growth effects of miR-129 on gastric cancer cells, we found that all three mature products of miR-129 showed tumor suppressor activities. To elucidate the molecular mechanisms underlying down-regulation of miR-129 in gastric cancer, we analyzed the effects of miR-129 mimics on the cell cycle. We found that increased miR-129 levels in gastric cancer cells resulted in significant G(0)/G(1) phase arrest. Interestingly, we showed that cyclin dependent kinase 6 (CDK6), a cell cycle-associated protein involved in G(1)-S transition, was a target of miR-129. We also found that expression of the sex determining region Y-box 4 (SOX4) was inversely associated with that of miR-129-2-3p and miR-129-5p but not of miR-129-1-3p. Together, our data indicate that all miR-129 family members, not only miR-129-5p, as previously thought, play an important role in regulating cell proliferation in gastric cancer. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 93
页数:7
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