作者: Li-Li Zhang , Yan-Jun Guo , Chun-Na Zhao , Jian-Yun Gao
DOI: 10.1016/S1995-7645(14)60350-3
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摘要: Abstract Objective To explore the role of miR-214 in progression hepatocellular carcinoma (HCC) and its inhibitory mechanisms depressing signaling pathway β-catenin, this study was conducted. Methods We ectopically expressed HepG2 cells to obtain cell lines Lv-miR-214-HepG2 their control Lv-control-HepG2. Differences between two were compared growth, proliferation, colony forming ability cycles. RT-PCR method applied for quantification β-catenin mRNA expression. Western-blot determination protein level downstream targets (ie. Cyclin D1, c-Myc TCF-1). The effect on further explored through RNA interference restoring Results In comparison with negative (Lv-control-HepG2) blank (HepG2) control, a significant inhibition growth proliferation caused by observed after 48∼72h culture experiments ( P 0 /G 1 phase [(70.32±3.12)%] but lower proportion S [(18.42±2.90)%] >0.05). By comparing results treatment led slightly decrease expression >0.05), an extremely c-Myc, TCF-1 Conclusions functions as suppressor during HCC, achieved down-regulating pathway.