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首页> 外文期刊>World journal of gastroenterology : >Anti-tumor effect of 5-aza-2'-deoxycytidine by inhibiting telomerase activity in hepatocellular carcinoma cells.
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Anti-tumor effect of 5-aza-2'-deoxycytidine by inhibiting telomerase activity in hepatocellular carcinoma cells.

机译:5-氮杂-2'-脱氧胞苷通过抑制肝癌细胞端粒酶活性的抗肿瘤作用。

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摘要

To investigate the effect of the demethylating reagent 5-aza-2'-deoxycitidine (DAC) on telomerase activity in hepatocellular carcinoma (HCC) cell lines, SMMC-7721 and HepG2.The related gene expression in cell lines was examined by real-time reverse transcription-polymerase chain reaction and Western blotting analysis. The telomerase activity was examined by telomeric repeat amplification protocol-enzyme-linked immunosorbent assay and DNA methylation was determined by methylation-specific polymerase chain reaction.The telomerase activity was significantly reduced in both cell lines treated with DAC, accompanied by downregulation of telomerase reverse transcriptase (hTERT). We also observed the effect of DAC on the methylation status of hTERT promoter and the expression of regulatory genes, such as c-myc, p15, p16, p21, E2F1, and WT1. The methylation status of hTERT promoter could be reversed in SMMC-7721 by DAC, but not in HepG2 cells. However, p16 expression could be reactivated by demethylation of its promoter, and c-Myc expression was repressed in both cell lines. Moreover, DAC could enhance the sensitivity to the chemotherapeutic agents, such as cisplatin, by induction of apoptosis of HCC cells.The DAC exerts its anti-tumor effects in HCC cells by inhibiting the telomerase activity.
机译:为了研究去甲基化试剂5-氮杂2'-脱氧胞苷(DAC)对肝癌细胞(SMCC-7721)和HepG2端粒酶活性的影响,实时检测了相关基因的表达逆转录聚合酶链反应和蛋白质印迹分析。通过端粒重复扩增方案-酶联免疫吸附试验检测端粒酶活性,并通过甲基化特异性聚合酶链反应测定DNA甲基化。在DAC处理的两种细胞系中,端粒酶活性均显着降低,同时端粒酶逆转录酶表达下调(hTERT)。我们还观察到DAC对hTERT启动子甲基化状态和调节基因(例如c-myc,p15,p16,p21,E2F1和WT1)表达的影响。 hTERT启动子的甲基化状态可以在DAC中在SMMC-7721中逆转,但在HepG2细胞中则不能逆转。但是,p16的表达可以通过其启动子的去甲基化来重新激活,并且在两种细胞系中c-Myc的表达都被抑制。此外,DAC可以通过诱导HCC细胞凋亡来增强对顺铂等化学治疗药物的敏感性.DAC通过抑制端粒酶活性在HCC细胞中发挥其抗肿瘤作用。

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