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miR-101 suppresses HBV replication and expression by targeting FOXO1 in hepatoma carcinoma cell lines

机译:miR-101通过靶向肝癌癌细胞系中的FOXO1来抑制HBV复制和表达

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microRNAs (miRNAs) have been identified to participate in the progression of cancers and in the infection of viruses. miR-101 expression has been found to be suppressed by HBV, however, the regulatory relationship between miR-101 and HBV replication remains elusive. In this report, miR-101 was significantly downregulated in HepG2.2.15 cells with HBV expression. miR-101 overexpression dramatically suppressed HBV replication and expression. Oppositely, overexpression of FOXO1 significantly promoted HBV replication and expression. Moreover, luciferase reporter analysis, qRT-PCR analysis and western blot assay confirmed that FOXO1 was a functional target of miR-101. Furthermore, restored FOXO1 expression abolished the inhibitory effect of miR-101 overexpression on HBV replication and expression in HepG2.2.15 cells. Our data suggested that miR-101 suppressed HBV replication and expression partially by targeting FOXO1, providing new insights into the molecular mechanisms of miR-101 in HBV-host interactions and a promising therapeutic target for HBV replication. (C) 2017 Elsevier Inc. All rights reserved.
机译:已经鉴定了MicroRNA(miRNA)参与癌症的进展和病毒感染。已经发现miR-101表达被HBV抑制,但是,MiR-101和HBV复制之间的监管关系仍然难以捉摸。在本报告中,MIR-101在HBV表达中显着下调HepG2.2.15细胞。 miR-101过表达显着抑制了HBV复制和表达式。相反,FoxO1的过表达显着促进了HBV复制和表达。此外,荧光素酶报告者分析,QRT-PCR分析和蛋白质印迹测定证实FoxO1是miR-101的功能靶标。此外,恢复的FOXO1表达废除了MIR-101过表达对HPG2.2.15细胞HBV复制和表达的抑制作用。我们的数据表明MIR-101通过靶向FOXO1抑制HBV复制和表达,从HBV-宿主相互作用中的miR-101的分子机制和HBV复制的有前途治疗靶标的新见解。 (c)2017年Elsevier Inc.保留所有权利。

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