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首页> 外文期刊>Acta Biochimica Polonica >Quantitative analysis of the level of p53 and p21(WAF1) mRNA in human colon cancer HT-29 cells treated with inositol hexaphosphate
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Quantitative analysis of the level of p53 and p21(WAF1) mRNA in human colon cancer HT-29 cells treated with inositol hexaphosphate

机译:六磷酸肌醇处理人结肠癌HT-29细胞中p53和p21(WAF1)mRNA水平的定量分析

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The aim of this study was to analyze the molecular mechanism of inositol hexaphosphate (InsP(6)) action through which it may inhibit proliferation of colon cancer cells and cell cycle progression. A kinetic study of p53 and p21(WAF1) mRNA increase was performed on human colon cancer HT-29 cells after treatment with 1, 5 and 10 mM InsP(6) for 6, 12, 24 and 48 h. Real-time-QPCR based on TaqMan methodology was applied to analyze quantitatively the transcript levels of these genes. The transcription of beta-actin and GAPDH genes was assessed in parallel to select the control gene with least variability. The 2-(Delta Delta Ct) method was used to analyze the relative changes in gene transcription, InsP(6) stimulated p53 and p21(WAF1) expression at the mRNA level with the highest increase in p21(WAF1) mRNA occurring at 24 h, i.e., following the highest increase in p53 mRNA observed at 12 h. Based on these studies it may be concluded that the ability of InsP(6) to arrest the cell cycle may be mediated by the transcriptional up-regulation of the p53-responsive p21(WAF1) gene.
机译:这项研究的目的是分析肌醇六磷酸(InsP(6))作用的分子机制,通过它可以抑制结肠癌细胞的增殖和细胞周期的进程。在用1、5和10 mM InsP(6)处理6、12、24和48小时后,对人结肠癌HT-29细胞进行了p53和p21(WAF1)mRNA增加的动力学研究。基于TaqMan方法的实时QPCR被用于定量分析这些基因的转录水平。并行评估β-肌动蛋白和GAPDH基因的转录,以选择变异性最小的对照基因。 2-(Delta Delta Ct)方法用于分析基因转录的相对变化,InsP(6)刺激了mRNA表达水平的p53和p21(WAF1)表达,其中24小时出现的p21(WAF1)mRNA增幅最大。即在12 h观察到p53 mRNA的最高增加。基于这些研究,可以得出结论,InsP(6)阻止细胞周期的能力可能是由p53反应性p21(WAF1)基因的转录上调介导的。

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