首页> 外文期刊>Experimental & Molecular Pathology >Induction of apoptosis and inhibition of telomerase activity by trichostatin A, a histone deacetylase inhibitor, in human leukemic U937 cells.
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Induction of apoptosis and inhibition of telomerase activity by trichostatin A, a histone deacetylase inhibitor, in human leukemic U937 cells.

机译:组蛋白脱乙酰基酶抑制剂曲古抑菌素A在人白血病U937细胞中诱导凋亡和抑制端粒酶活性。

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The objective of the present study was to investigate the effect of trichostatin A (TSA), a histone deacetylase (HDAC) inhibitor, on the cell growth and apoptosis and its effect on the telomerase activity in human leukemic cell line U937. Exposure of U937 cells to TSA resulted in growth inhibition and induction of apoptosis in a dose-dependent manner as measured by hemocytometer counts, fluorescence microscopy, agarose gel electrophoresis and flow cytometry analysis. The increase in apoptosis was associated with the up-regulation in proapoptotic Bax expression and down-regulation of antiapoptotic Bcl-2 and Bcl-X(L). TSA treatment inhibited the levels of cIAP family members and induced the proteolytic activation of caspase-3, which was associated with concomitant degradation of poly(ADP-ribose)-polymerase and beta-catenin protein. TSA treatment markedly inhibited the activity of telomerase in a dose-dependent fashion. Additionally, the expression of human telomerase reverse transcriptase (hTERT), a maindeterminant of the telomerase enzymatic activity, was progressively down-regulated by TSA treatment. We therefore conclude that TSA demonstrated antiproliferative and apoptosis-inducing effects on U937 cells in vitro, and that changes in Bcl-2 family protein levels as well as telomerase activity may play an important role in its mechanism of action.
机译:本研究的目的是研究组蛋白脱乙酰基酶(HDAC)抑制剂曲古抑菌素A(TSA)对人白血病细胞系U937中细胞生长和凋亡的影响及其对端粒酶活性的影响。 U937细胞暴露于TSA导致生长抑制和凋亡诱导,其剂量依赖性通过血细胞计数器,荧光显微镜,琼脂糖凝胶电泳和流式细胞仪分析进行测量。凋亡的增加与凋亡前Bax表达的上调和抗凋亡Bcl-2和Bcl-X(L)的下调相关。 TSA处理抑制cIAP家族成员的水平并诱导caspase-3的蛋白水解激活,这与聚(ADP-核糖)-聚合酶和β-连环蛋白的降解有关。 TSA处理以剂量依赖性方式显着抑制端粒酶的活性。另外,通过TSA处理,人端粒酶逆转录酶(hTERT)的表达是端粒酶酶活性的主要决定因素,hTERT的表达逐渐下调。因此,我们得出结论,TSA在体外对U937细胞表现出抗增殖和凋亡诱导作用,并且Bcl-2家族蛋白水平以及端粒酶活性的变化可能在其作用机理中起重要作用。

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