| Literature DB >> 27490780 |
Huaqiang Zhu1, Guangchuan Wang2, Xu Zhou1, Xie Song1, Hengjun Gao1, Chaoqun Ma1, Hong Chang1, Hongguang Li1, Fang-Feng Liu1, Jun Lu1, Jinben Ma3.
Abstract
microRNA (miRNA) plays critical role in HCC initiation and development, many miRNAs have been reported to regulate HCC progression. In this study, we studied the role of miR-1299 in cell proliferation of HCC. We found miR-1299 was significantly downregulated in HCC cells and tissues. miR-1299 overexpression inhibited cell proliferation and arrested cell cycle in G0/G1 phase analyzed by MTT assay, soft agar assay, BrdU cell proliferation assay and cell cycle assay, while miR-1299 knockdown promoted cell proliferation and accelerated G1/S transition. Further analysis suggested the key regulator of G1/S transition, cyclin-dependent kinase 6 (CDK6) was the target of miR-1299, miR-1299 inhibited CDK6 expression and bound to the 3'UTR of CDK6. When double knockdown of miR-1299 and CDK6 promoted cell proliferation copied the phenotype caused by miR-1299 overexpression, suggesting miR-1299 inhibits cell proliferation by targeting CDK6. In summary, our data revealed miR-1299 inhibits cell proliferation, and might be a target for HCC therapy.Entities:
Keywords: CDK6; Cell proliferation; HCC; miR-1299
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Year: 2016 PMID: 27490780 DOI: 10.1016/j.biopha.2016.07.037
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529