Effect of microRNA-148b and microRNA-152 on proliferation and apoptosis of cholangiocarcinoma cells
Kun Cao, Liangquan Sun, Yongjun Gong, Tao Zhang, Haiyang Li
Abstract
Kun Cao, Liangquan Sun, Yongjun Gong, Tao Zhang, Haiyang Li
Abstract
Objective To investigate the microRNA (miRNA, miR)-148b and miR-152 expression and their biological functions in cholangiocarcinoma cells. Methods The expression levels of miR-148b and miR-152 in cholangiocarcinoma simples and QBC939 cells were detected using real-time quantitative polymerase chain reaction (Real-time PCR). After transfection with miR-148b/miR-152 mimics, cell proliferation, cell cycle and apoptosis were assessed using methyl thiazol tetrazolium (MTT) method, clone formation test and flow cytometry, respectively. Results The expression levels of miR-148b and miR-152 were significantly down-regulated [(2.75±0.16) folds and (3.05±0.18) folds] in cholangiocarcinoma samples as compared with normal samples (P=0.013, 0.019, respectively), and [(2.52±0.03) folds and (3.96±0.02) folds] in QBC939 cells as compared with H-69 cells (P=0.018, 0.012, respectively). Overexpression of miR-148b or miR-152 could significantly inhibit cell proliferation [(38.49±0.31)% and (52.69±1.01)%, respectively], and suppress cell clone formation (P=0.027, 0.017, respectively), block cell cycle in the S phase and induce cell apoptosis. Conclusion MiR-148b and miR-152 were down-regulated in cholangiocarcinoma cells, and overexpression of miR-148b and miR-152 could inhibit cell proliferation and induce cell apoptosis. Key words: MicroRNA-148b; MicroRNA-152; Cholangiocarcinoma; Proliferation; Apoptosis
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Objective To investigate the microRNA (miRNA, miR)-148b and miR-152 expression and their biological functions in cholangiocarcinoma cells. Methods The expression levels of miR-148b and miR-152 in cholangiocarcinoma simples and QBC939 cells were detected using real-time quantitative polymerase chain reaction (Real-time PCR). After transfection with miR-148b/miR-152 mimics, cell proliferation, cell cycle and apoptosis were assessed using methyl thiazol tetrazolium (MTT) method, clone formation test and flow cytometry, respectively. Results The expression levels of miR-148b and miR-152 were significantly down-regulated [(2.75±0.16) folds and (3.05±0.18) folds] in cholangiocarcinoma samples as compared with normal samples (P=0.013, 0.019, respectively), and [(2.52±0.03) folds and (3.96±0.02) folds] in QBC939 cells as compared with H-69 cells (P=0.018, 0.012, respectively). Overexpression of miR-148b or miR-152 could significantly inhibit cell proliferation [(38.49±0.31)% and (52.69±1.01)%, respectively], and suppress cell clone formation (P=0.027, 0.017, respectively), block cell cycle in the S phase and induce cell apoptosis. Conclusion MiR-148b and miR-152 were down-regulated in cholangiocarcinoma cells, and overexpression of miR-148b and miR-152 could inhibit cell proliferation and induce cell apoptosis. Key words: MicroRNA-148b; MicroRNA-152; Cholangiocarcinoma; Proliferation; Apoptosis
Key concepts: microRNA, Apoptosis, Flow cytometry, Cell cycle, Cell growth, Transfection, clone (Java method), Molecular biology