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LAMC1 mRNA Promotes Malignancy of Hepatocellular Carcinoma Cells by Competing for MicroRNA-124 Binding with CD151

机译:LAMC1 mRNA通过竞争CD151的MicroRNA-124结合来促进肝细胞癌细胞的恶性肿瘤

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摘要

Specific RNAs can function as sinks for endogenous miRNAs, known as competing endogenous RNAs (ceRNAs). Here, we confirm a miR-124 mediated ceRNA crosstalk between LAMC1 and CD151 in hepatocellular carcinoma (HCC). miR-124 negatively regulates LAMC1 expression through two miRNA binding sites within its 3' untranslated region (3'UTR) and suppresses migration and invasion of HCC cells through regulating LAMC1. The wild type LAMC1 miRNA response elements (MREs) facilitate expression of CD151, and this regulation is miR-124 dependent. In clinical hepatic tissues, LAMC1 and CD151 mRNAs exhibit positive correlation. Importantly, LAMC1 MREs promote HCC malignancy by absorbing miR-124 and by assisting CD151 expression. We conclude that LAMC1 mRNA acts as a trans regulator to stimulate CD151 expression by competing for miR-124 binding in HCC cells. (C) 2017 IUBMB Life
机译:特定的RNA可以用作内源性miRNA的沉积,称为竞争内源性RNA(CERNAS)。 在这里,我们在肝细胞癌(HCC)中,在LAMC1和CD151之间确认MIR-124介导的Cerna串扰。 MiR-124通过其3'未转换区域(3'UTR)内的两个miRNA结合位点来负调节LAMC1表达,并通过调节LAMC1来抑制HCC细胞的迁移和侵袭。 野生型LAMC1 miRNA反应元件(MRE)促进CD151的表达,并且该调节是miR-124依赖性。 在临床肝组织中,LAMC1和CD151 mRNA表现出正相关。 重要的是,LAMC1 MRE通过吸收miR-124并通过辅助CD151表达来促进HCC恶性肿瘤。 我们得出结论,LAMC1 mRNA充当反式调节剂以通过竞争HCC细胞中的miR-124结合来刺激CD151表达。 (c)2017年IUBMB生活

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