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Effect of pseudolaric acid B on gastric cancer cells: inhibition of proliferation and induction of apoptosis.

机译:伪laric acid B对胃癌细胞的作用:抑制增殖和诱导凋亡。

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AIM: To examine the effect of pseudolaric acid B on the growth of human gastric cancer cell line, AGS, and its possible mechanism of action. METHODS: Growth inhibition by pseudolaric acid B was analyzed using MTT assay. Apoptotic cells were detected using Hoechst 33258 staining, and confirmed by DNA fragmentation analysis. Western blot was used to detect the expression of apoptosis-regulated gene Bcl-2, caspase 3, and cleavage of poly (ADP-ribose) polymerase-1 (PARP-1). RESULTS: Pseudolaric acid B inhibited the growth of AGS cells in a time- and dose-dependent manner by arresting the cells at G(2)/M phase, which was accompanied with a decrease in the levels of cdc2. AGS cells treated with pseudolaric acid B showed typical characteristics of apoptosis including chromatin condensation and DNA fragmentation. Moreover, treatment of AGS cells with pseudolaric acid B was also associated with decreased levels of the anti-apoptotic protein Bcl-2, activation of caspase-3, and proteolytic cleavage of PARP-1. CONCLUSION: Pseudolaric acid B can dramatically suppress the AGS cell growth by inducing apoptosis after G(2)/M phase arrest. These findings are consistent with the possibility that G(2)/M phase arrest is mediated by the down-regulation of cdc2 levels. The data also suggest that pseudolaric acid B can trigger apoptosis by decreasing Bcl-2 levels and activating caspase-3 protease.
机译:目的:研究假laric acid B对人胃癌细胞AGS生长的影响及其可能的作用机制。方法:采用MTT分析法分析伪油酸B对生长的抑制作用。使用Hoechst 33258染色检测凋亡细胞,并通过DNA片段分析进行确认。 Western印迹用于检测凋亡调控基因Bcl-2,caspase 3的表达以及多聚(ADP-核糖)聚合酶-1(PARP-1)的切割。结果:伪laric B通过将细胞停滞在G(2)/ M期,以时间和剂量依赖性的方式抑制了AGS细胞的生长,并伴随着cdc2水平的降低。用伪laric acid B处理的AGS细胞显示出典型的凋亡特征,包括染色质浓缩和DNA片段化。此外,用伪油酸B处理AGS细胞还与抗凋亡蛋白Bcl-2的水平降低,胱天蛋白酶3的活化以及PARP-1的蛋白水解裂解有关。结论:伪laric B能诱导G(2)/ M期停滞后诱导细胞凋亡,从而显着抑制AGS细胞的生长。这些发现与G(2)/ M阶段逮捕由下调cdc2水平介导的可能性是一致的。数据还表明,假laric acid B可以通过降低Bcl-2水平和激活caspase-3蛋白酶来触发细胞凋亡。

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