| Literature DB >> 30961699 |
Wenjian Jin1, Ning Zhong2, Lingling Wang2, Jieli Yu2, Fugen Yin2, Kunhe Zhang3.
Abstract
MicroRNAs play an important role in cell proliferation and migration in hepatocellular carcinoma (HCC). In this study, the expression of MiR-331-3p in the liver cancer tissues of 116 patients, and in one normal (HL-7702) and five HCC cell lines (HepG2, SMMC-7721, Bel-7402, QGY-7701 and QGY-7703) was determined by qRT-PCR. Results indicated that MiR-331-3p was significantly repressed in HCC patients and in HCC cell lines, especially in the Bel-7402 cells when compared to normal liver tissue and the normal hepatocyte line, HL-7702. Therefore, artificial MiR-331-3p mimic computationally targeting E2F1 and anti-sense MiR-331-3p inhibitor were designed and used to transfect the Bel-7402 lines. Stable expression and significant inhibition of MiR-331-3p, with clear changes in cell morphology, proliferation and motility, were detected in Bel-7402 cells transfected with MiR-331-3p mimic or inhibitor, respectively. As E2F1 was computationally recognized as the target of MiR-331-3p, the expression of E2F1 in transfected Bel-7402 cells was analyzed by qRT-PCR and Western blotting. Results showed a strong inhibition of E2F1 by MiR-331-3p and further promotion of E2F1 by MiR-331-3p inhibitor in transfected Bel-7402 cells. Flow cytometry analysis showed that the cell ratio was restored to S to G0/1 cell number. Inhibition of E2F1 by MiR-331-3p mimic promoted cell proliferation and migration in Bel-7402. These results demonstrated that MiR-331-3p down-regulated E2F1 to promote cell proliferation and migration in HCC.Entities:
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Year: 2019 PMID: 30961699 DOI: 10.1166/jnn.2019.16535
Source DB: PubMed Journal: J Nanosci Nanotechnol ISSN: 1533-4880