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首页> 外文期刊>Oncology reports >Anti-apoptotic and apoptotic pathway analysis of arsenic trioxide-induced apoptosis in human gastric cancer SGC-7901 cells
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Anti-apoptotic and apoptotic pathway analysis of arsenic trioxide-induced apoptosis in human gastric cancer SGC-7901 cells

机译:三氧化二砷诱导人胃癌SGC-7901细胞凋亡的抗凋亡和凋亡途径分析

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The present study aimed to investigate the effect of arsenic trioxide (As2O3) on human gastric cancer SGC-7901 cells. SGC-7901 cells were treated with different concentrations of As2O3 in the cell growth media for 24, 48 and 72 h, and the growth rates were determined by WST-1 cell proliferation assays. Analyses of nuclear morphological changes were performed with DAPI fluorescence staining. Cell apoptosis rates as assessed by flow cytometry were determined after cells were grown in media for 48 h containing different As2O3 concentrations. The protein expression patterns of the apoptosis factors, Bax, Fas and caspase-8, and anti-apoptosis factors, Akt, p-Akt, mTOR and p-mTOR, were evaluated by western blot analysis following treatment of the cells with different As2O3 concentrations in the cell growth media for 48 h. As a result, As2O3 inhibited the growth of human gastric cancer SGC-7901 cells in concentrations >5 mu mol/I for longer than 24 h. Flow cytometric analysis revealed that the apoptosis of SGC-7901 cells occurred in an As2O3 concentration-dependent manner after 48 h (P<0.001). Expression levels of Bax, Fas and caspase-8 were increased, whereas expression levels of Akt, p-Akt, mTOR and p-mTOR were decreased in the SGC-7901 cells after a 48-h incubation with different As2O3 concentrations. In conclusion, As2O3 induced human gastric cancer SGC-7901 cell apoptosis in a time- and concentration dependent manner by inhibiting the activity of anti-apoptosis-related factors.
机译:本研究旨在研究三氧化二砷(As2O3)对人胃癌SGC-7901细胞的作用。在细胞生长培养基中用不同浓度的As2O3处理SGC-7901细胞24、48和72小时,并通过WST-1细胞增殖测定法确定其生长速率。用DAPI荧光染色进行核形态变化的分析。细胞在含有不同浓度的As2O3的培养基中生长48小时后,通过流式细胞术确定细胞凋亡率。在用不同浓度的As2O3处理细胞后,通过蛋白质印迹分析评估了凋亡因子Bax,Fas和caspase-8的蛋白表达模式,以及抗凋亡因子Akt,p-Akt,mTOR和p-mTOR的蛋白表达模式。在细胞生长培养基中放置48小时。结果,As2O3抑制人类胃癌SGC-7901细胞的浓度> 5μmol / I的时间超过24小时。流式细胞仪分析显示,SGC-7901细胞在48 h后以As2O3浓度依赖性的方式发生凋亡(P <0.001)。在不同浓度的As2O3中孵育48小时后,SGC-7901细胞中Bax,Fas和caspase-8的表达水平增加,而Akt,p-Akt,mTOR和p-mTOR的表达水平降低。总之,As2O3通过抑制抗凋亡相关因子的活性以时间和浓度依赖性方式诱导人胃癌SGC-7901细胞凋亡。

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