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MiR-211 promotes invasion of hepatoma cells by targeting estrogen receptor alpha / 中华肝脏病杂志
Chinese Journal of Hepatology ; (12): 527-532, 2015.
Article in Chinese | WPRIM | ID: wpr-290430
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the regulatory functions and molecular mechanisms of miR211 in hepatocellular carcinoma (HCC).</p><p><b>METHODS</b>Real-time reverse transcription-PCR was used to analyze the expression of miR-211 in 20 paired clinical specimens of HCC and adjacent noncancerous tissues.QGY7703 and HepG2 cells with stimulation or inhibition of miR-211 expression were used to evaluate the effects on malignant phenotypes with the transwell invasion assay. Candidate target genes of miR-211 were identified by bioinformatic screening and verified by the EGFP report assay, real-time PCR and western blotting. Moreover, the regulatory functions of miR-211 on the target genes were investigated by RNA interference and cell phenotype assays.</p><p><b>RESULTS</b>miR-211 was up-regulated in HCC tissue specimens (t =6.26, P < 0.01).HCC cells overexpressing miR-211 showed greater invasive capacity than cells with inhibited expression (QGY-7703t =12.59, P < 0.01; HepG2 t =17.82, P < 0.01). Estrogen receptor a (ESR1) was identified and validated as a target gene of miR-211; knockdown of ESR 1 promoted HCC invasive capacity (QGY-7703t =8.97, P < 0.01; HepG2t =29.31, P < 0.01).</p><p><b>CONCLUSION</b>miR-211 promotes invasion of carcinoma cells by directly targeting ESR1.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Carcinoma, Hepatocellular / MicroRNAs / RNA Interference / Cell Line, Tumor / Estrogen Receptor alpha / Real-Time Polymerase Chain Reaction / Liver Neoplasms Limits: Humans Language: Chinese Journal: Chinese Journal of Hepatology Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Carcinoma, Hepatocellular / MicroRNAs / RNA Interference / Cell Line, Tumor / Estrogen Receptor alpha / Real-Time Polymerase Chain Reaction / Liver Neoplasms Limits: Humans Language: Chinese Journal: Chinese Journal of Hepatology Year: 2015 Type: Article