首页> 美国卫生研究院文献>International Journal of Oncology >Regulation of Id1 expression by epigallocatechin-3-gallate and its effect on the proliferation and apoptosis of poorly differentiated AGS gastric cancer cells
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Regulation of Id1 expression by epigallocatechin-3-gallate and its effect on the proliferation and apoptosis of poorly differentiated AGS gastric cancer cells

机译:表没食子儿茶素-3-没食子酸酯调节Id1表达及其对低分化AGS胃癌细胞增殖和凋亡的影响

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摘要

We investigated the inhibition of apoptosis and proliferation of poorly differentiated AGS gastric cancer cells by epigallocatechin-3-gallate (EGCG), to establish target genes for regulation by EGCG. The proliferation and apoptosis of AGS gastric cancer cells treated with EGCG were observed by cell counting kit (CCK)-8 and flow cytometry. Differential gene expression in AGS cells treated with EGCG was screened by gene expression microarrays. Id1 gene and protein expression were determined by quantitative PCR and western blot analysis. The effect of Id1 on EGCG-induced apoptosis and cell cycle arrest of AGS cells was verified with RNAi. The proliferation and apoptosis of AGS cells treated with siRNA-Id1 was observed by CCK-8 and flow cytometry. EGCG significantly promoted apoptosis and inhibited the proliferation of AGS cells. The Id1 gene was differentially expressed in AGS cells treated with EGCG, and Id1 mRNA and protein were downregulated in AGS cells treated with EGCG, confirmed by quantitative PCR and western blot analysis. Id1 mRNA and protein were also downregulated in AGS cells treated with siRNA-Id1. The apoptosis and proliferation of AGS cells treated with siRNA-Id1 were similar to those in cells treated with EGCG. EGCG induces apoptosis and inhibits proliferation of poorly differentiated AGS gastric cancer cells, and Id1 may be one of the target genes regulated by EGCG in cancer inhibition.
机译:我们研究了Epigallocatechin-3-gallate(EGCG)对低分化AGS胃癌细胞的凋亡和增殖的抑制作用,以建立由EGCG调控的靶基因。用细胞计数试剂盒(CCK)-8和流式细胞仪观察EGCG处理的AGS胃癌细胞的增殖和凋亡。通过基因表达微阵列筛选在EGCG处理的AGS细胞中的差异基因表达。通过定量PCR和蛋白质印迹分析确定Id1基因和蛋白质表达。 RNAi证实了Id1对EGCG诱导的AGS细胞凋亡和细胞周期阻滞的影响。通过CCK-8和流式细胞术观察了用siRNA-Id1处理的AGS细胞的增殖和凋亡。 EGCG显着促进凋亡并抑制AGS细胞的增殖。通过定量PCR和Western印迹分析证实,在用EGCG处理的AGS细胞中Id1基因差异表达,在用EGCG处理的AGS细胞中Id1 mRNA和蛋白下调。在用siRNA-Id1处理的AGS细胞中,Id1 mRNA和蛋白质也下调。 siRNA-Id1处理的AGS细胞的凋亡和增殖与EGCG处理的细胞相似。 EGCG诱导低分化AGS胃癌细胞凋亡并抑制其增殖,Id1可能是EGCG调控的靶基因之一。

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