Downregulated miR-621 promotes cell proliferation via targeting CAPRIN1 in hepatocellular carcinoma

被引:1
|
作者
Zhang, Yao [1 ]
You, Wei [1 ]
Zhou, Haoming [1 ]
Chen, Zhiqiang [1 ]
Han, Guoyong [1 ]
Zuo, Xueliang [1 ,2 ]
Zhang, Long [1 ]
Wu, Jindao [1 ,3 ]
Wang, Xuehao [1 ]
机构
[1] Nanjing Med Univ, Chinese Acad Med Sci, Key Lab Liver Transplantat, Hepatobiliary Ctr,Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[2] Wannan Med Coll, Yijishan Hosp, Affiliated Hosp 1, Dept Gastrointestinal Surg, Wuhu 241001, Peoples R China
[3] Nanjing Med Univ, State Key Lab Reprod Med, Nanjing 210029, Jiangsu, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2018年 / 8卷 / 10期
基金
中国国家自然科学基金;
关键词
HCC; miR-621; CAPRIN1; proliferation; TUMOR-GROWTH; COLON-CANCER; MICRORNAS; EXPRESSION; HETEROZYGOSITY; METASTASIS; BIOGENESIS; PROTEIN; 13Q; MYC;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) have been reported to play an essential role in tumor development and progression. However, the function of miR-621 in hepatocellular carcinoma (HCC) remains largely unexplored. In this study, we found that miR-621 was downregulated in the HCC specimens and cell lines, and lower expression of miR-621 indicated poor survival. Overexpression of miR-621 was shown to induce G0/G1 cell cycle arrest and inhibit cell proliferation in vitro and in vivo. Luciferase assays revealed that cell cycle-associated protein 1 (CAPRIN1) is a novel functional downstream target of miR-621. miR-621 could regulate c-MYC and cyclin D2 expression by directly targeting CAPRIN1. Further study revealed that CAPRIN1 was upregulated in the HCC specimens and cell lines. Restoration of CAPRIN1 neutralized the miR-621-induced cell cycle arrest and cell proliferation inhibition. Taken together, our findings suggest that miR-621 acts as a tumor suppressor gene in HCC progression by downregulating CAPRIN1 expression and could be a novel potential diagnostic and prognostic biomarker for HCC.
引用
收藏
页码:2116 / +
页数:16
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