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邹宁, 袁成良, 刘朝红, 许丹. 微小RNA-340对肝癌细胞增殖和凋亡的影响[J]. 肿瘤防治研究, 2017, 44(11): 724-727. DOI: 10.3971/j.issn.1000-8578.2017.17.0063
引用本文: 邹宁, 袁成良, 刘朝红, 许丹. 微小RNA-340对肝癌细胞增殖和凋亡的影响[J]. 肿瘤防治研究, 2017, 44(11): 724-727. DOI: 10.3971/j.issn.1000-8578.2017.17.0063
ZOU Ning, YUAN Chengliang, LIU Chaohong, XU Dan. Effect of MicroRNA-340 on Proliferation and Apoptosis of Hepatocellular Carcinoma Cell Lines[J]. Cancer Research on Prevention and Treatment, 2017, 44(11): 724-727. DOI: 10.3971/j.issn.1000-8578.2017.17.0063
Citation: ZOU Ning, YUAN Chengliang, LIU Chaohong, XU Dan. Effect of MicroRNA-340 on Proliferation and Apoptosis of Hepatocellular Carcinoma Cell Lines[J]. Cancer Research on Prevention and Treatment, 2017, 44(11): 724-727. DOI: 10.3971/j.issn.1000-8578.2017.17.0063

微小RNA-340对肝癌细胞增殖和凋亡的影响

Effect of MicroRNA-340 on Proliferation and Apoptosis of Hepatocellular Carcinoma Cell Lines

  • 摘要:
    目的 探讨过表达miR-340对人肝癌HepG2、MHCC-97L细胞增殖、细胞周期和凋亡的影响。
    方法 miR-340 mimic转染后RT-PCR法测定肝癌细胞株miR-340 mRNA水平,Brdu-ELISA试剂盒检测细胞增殖,流式细胞术分析细胞周期,膜联蛋白V-FITC凋亡检测试剂盒分析细胞凋亡。
    结果 miR-340在肝癌细胞系中表达降低(P < 0.05);高表达miR-340后肝癌细胞的存活率受到显著抑制(P < 0.05);G0/G1期细胞增多(P < 0.05);S期细胞减少(P < 0.05);高表达miR-340后HepG2和MHCC-97L细胞凋亡受到促进(P < 0.05)。
    结论 miR-340在抑制细胞增殖、NF-κB1下调诱导的细胞凋亡中起着重要的作用,提示miR-340表达降低是肝细胞肝癌发生的机制之一。

     

    Abstract:
    Objective To explore the effect of miR-340 overexpression on cell proliferation, cell cycle and apoptosis of human hepatocellular carcinoma HepG2 and MHCC-97L cells.
    Methods The miR-340 mimic was transiently transfected into HCC cells using LipofectamineTM 2000 reagent. The mRNA level of miR-340 in HCC cell lines was determined by RT-PCR. Cell proliferation was detected by Brdu-ELISA kit. Flow cytometry was used to analyze cell cycle. Apoptosis was analyzed by Annexin V-FITC apoptosis detection kit.
    Results The expression of miR-340 was decreased in HepG2 and MHCC-97L cells (P < 0.05); miR-340 overexpression significantly inhibited cell survival rate (P < 0.05); the percentage of cells in G0/G1 stage was increased and that in the S stage was reduced (both P < 0.05); miR-340 overexpression promoted the apoptosis of HepG2 and MHCC-97L cells also.
    Conclusion miR-340 plays an important role in the inhibition of cell proliferation and the apoptosis induced by NF-κB1 down-regulation, suggesting that reduced miR-340 expression is one of the mechanisms of hepatocellular carcinogenesis.

     

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