| Literature DB >> 33598424 |
Hongxi Ma1, Chunchun Huang2, Qiuhuan Huang2, Guangzhi Li2, Jun Li2, Bin Huang2, Qiuhong Zhong3, Cong Cao2.
Abstract
Recent studies have reported a close association between circRNAs and cancer development. CircRNAs have been recognized to be involved in various biological processes. Up to now, the function of circRNAs in hepatocellular carcinoma (HCC) is still poorly known. qRT-PCR was used to test circ_0014717 expression in HCC tissue samples and cells was determined. It was shown that circ_0014717 was significantly decreased in HCC. Then, we observed overexpression of circ_0014717 obviously repressed HCC cell growth, migration and invasion. Next, we predicted circ_0014717 acted as a sponge of miR-668-3p. miR-668-3p has been reported to participate in several diseases. In our work, it was shown miR-668-3p was greatly increased in HCC and the direct binding sites between circ_0014717 and miR-668-3p were validated. In addition, B-cell translocation gene 2 (BTG2) is closely involved in cellular carcinogenic processes. BTG2 was predicted as a target for miR-668-3p. By performing rescue assays, we demonstrated that circ_0014717 repressed HCC progression via inhibiting BTG2 expression and sponging miR-668-3p. It was manifested loss of circ_0014717 induced HCC progression, which was reversed by BTG2 in Hep3B cells. In conclusion, our findings illustrated a novel circ_0014717/miR-668-3p/BTG2 regulatory signaling pathway in HCC.Entities:
Keywords: B-cell translocation gene 2; ceRNA; circ_0014717; hepatocellular carcinoma; miR-668-3p
Year: 2021 PMID: 33598424 PMCID: PMC7883829 DOI: 10.3389/fonc.2020.592884
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244