| Literature DB >> 29559347 |
Wei Zhang1, Sheng Qian2, Guowei Yang3, Liang Zhu4, Bo Zhou5, Jianhua Wang6, Rong Liu7, Zhiping Yan8, Xudong Qu9.
Abstract
Hepatocellular carcinoma (HCC), the most common primary tumor of the liver, has a poor prognosis and shows rapid progression. MicroRNAs (miRNAs) play important roles in carcinogenesis and tumor progression. Regulators of G-protein signaling (RGS) are critical for defining G-protein-dependent signal fidelity. RGS17 plays an important role in the regulation of cancer cell proliferation, migration and invasion. Here, we showed that miR-199 was downregulated in a hepatocarcinoma cell line. Overexpression of miR-199 significantly suppressed HCC cell proliferation, migration, and invasion in vitro. RGS17 overexpression promoted HCC cell proliferation, migration, and invasion, and reversed the miR-199 mediated inhibition of proliferation, migration, and invasion. Dual-fluorescence reporter experiments confirmed that miR-199 downregulated RGS17 by direct interaction with the 3'-UTR of RGS17 mRNA. In vivo studies showed that miR-199 overexpression significantly inhibited the growth of tumors. Taken together, the results suggested that miR-199 inhibited tumor growth and metastasis by targeting RGS17. Published by Elsevier B.V.Entities:
Keywords: Hepatocellular carcinoma; Migration; Proliferation; RGS17; miR-199
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Year: 2018 PMID: 29559347 DOI: 10.1016/j.gene.2018.03.053
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688