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5-azacytidine modulates gamma-glutamyltransferase and glutathione levelsin two human prostatic adenocarcinoma cell lines

机译:5-氮杂胞苷调节两种人前列腺腺癌细胞系中的γ-谷氨酰转移酶和谷胱甘肽水平

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摘要

Two human prostate adenocarcinoma cell lines, LNCaP and PC-3, were used to study the effect of 5-azacytidine on GGT gene expression, via genomic DNA methylation, and GSH content. When the cells were treated with 5-azaC, the specific GGT activity increased in a dose and time-dependent manner and was accompanied by the elevation of intracellular glutathione content. Southern blot analysis of DNA digested with MspI or HpaII showed negative correlation between the methylation pattern of GGT DNA and GCT activity, either in control or 5-azaC treated cells. Reverse transcription-polymerase chain reaction (RT-PCR) analysis revealed that GGT mRNA types I are expressed and induced in a cell type-specific manner in control and 5-azacC treated cells respectively. Overall, our investigations suggest that DNA methylation and other mechanisms combine to regulate GGT gene expression in studied prostate adenocarcinoma derived cells.
机译:使用两种人类前列腺腺癌细胞系LNCaP和PC-3,通过基因组DNA甲基化和GSH含量研究5-氮杂胞苷对GGT基因表达的影响。当用5-azaC处理细胞时,特异性GGT活性以剂量和时间依赖性方式增加,并伴随细胞内谷胱甘肽含量的升高。用MspI或HpaII消化的DNA的Southern印迹分析显示,在对照或5-azaC处理的细胞中,GGT DNA的甲基化模式与GCT活性之间呈负相关。逆转录-聚合酶链反应(RT-PCR)分析显示,GGT mRNA I型在对照和5-azacC处理的细胞中分别以细胞类型特异性方式表达和诱导。总的来说,我们的研究表明在研究的前列腺腺癌衍生细胞中,DNA甲基化和其他机制共同调节了GGT基因的表达。

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