首页> 外文期刊>The FEBS journal >Benzamide and 4-amino 1,8 naphthalimide treatment inhibit telomerase activity by down-regulating the expression of telomerase associated protein and inhibiting the poly(ADP-ribosyl)ation of telomerase reverse transcriptase in cultured cells
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Benzamide and 4-amino 1,8 naphthalimide treatment inhibit telomerase activity by down-regulating the expression of telomerase associated protein and inhibiting the poly(ADP-ribosyl)ation of telomerase reverse transcriptase in cultured cells

机译:苯甲酰胺和4-氨基1,8萘二甲酰亚胺处理可通过下调端粒酶相关蛋白的表达并抑制培养细胞中端粒酶逆转录酶的聚ADP-核糖基化来抑制端粒酶活性

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To test the role of poly(ADP-ribose) polymerase on the telomerase activity, we determined the telomerase activity in leukemic cells K562 treated with benzamide and 4-amino 1,8 naphthalimide (NAP), the inhibitors of PARP. We observed that both the agents inhibited telomerase activity in a dose-dependent manner. The doses of benzamide and NAP that inhibited telomerase activity to 50% of untreated control cells were 10.7 +/- 0.6 mM and 200 +/- 7 mu M, respectively. Benzamide treatment (10 mM) inhibited telomerase activity in a time-dependent manner. We also tested the ability of benzamide to inhibit the telomerase activity in Chinese hamster V79 cells and observed similar inhibition of the telomerase activity. Expression of telomerase reverse transcriptase (TERT) and telomerase RNA component, detected by RT-PCR, remained unaltered by treatment with benzamide or NAP. On the contrary, the expression of telomerase associated protein (TEP1/TP1), as detected by RT-PCR and western blot analysis, was reduced by both the agents. Further, in K562 cells, immunoprecipitation with the anti-TERT IgG and probed anti-poly (ADP-ribose) IgG revealed that TERT was poly(ADP-ribosyl)ated in the physiological condition of cell growth and such poly(ADP-ribosyl)ation was inhibited by benzamide treatment. Decrease in TEP1/TP1 expression and poly(ADP-ribosyl)ation of TERT were correlated with the inhibition of PARP activity by benzamide, indicating that PARP had a role in telomerase activity through poly(ADP-ribosyl)ation of TERT and down-regulation of TEP1/TP1.
机译:为了测试聚(ADP-核糖)聚合酶对端粒酶活性的作用,我们确定了苯甲酰胺和PARP抑制剂4-氨基1,8萘二甲酰亚胺(NAP)处理的白血病细胞K562中的端粒酶活性。我们观察到两种试剂均以剂量依赖性方式抑制端粒酶活性。抑制端粒酶活性的苯甲酰胺和NAP对未处理对照细胞的50%的剂量分别为10.7 +/- 0.6 mM和200 +/- 7μM。苯甲酰胺处理(10 mM)以时间依赖性方式抑制端粒酶活性。我们还测试了苯甲酰胺抑制中国仓鼠V79细胞端粒酶活性的能力,并观察到了类似的端粒酶活性抑制作用。通过RT-PCR检测到的端粒酶逆转录酶(TERT)和端粒酶RNA成分的表达通过苯甲酰胺或NAP处理仍保持不变。相反,两种试剂均降低了通过RT-PCR和Western blot分析检测到的端粒酶相关蛋白(TEP1 / TP1)的表达。此外,在K562细胞中,用抗TERT IgG和探测的抗聚(ADP-核糖)IgG进行免疫沉淀显示,TERT在细胞生长的生理条件下被聚(ADP-核糖)修饰,而这种聚(ADP-核糖)苯甲酰胺处理可抑制这种疾病。 TEP1 / TP1表达的降低和TERT的聚ADP-核糖基化与苯甲酰胺对PARP活性的抑制有关,表明PARP通过TERT的聚ADP-核糖基化和下调而在端粒酶活性中起作用TEP1 / TP1。

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