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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Apoptosis Induction by the Total Flavonoids fromArachniodes exilisin HepG2 Cells through Reactive Oxygen Species-Mediated Mitochondrial Dysfunction Involving MAPK Activation
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Apoptosis Induction by the Total Flavonoids fromArachniodes exilisin HepG2 Cells through Reactive Oxygen Species-Mediated Mitochondrial Dysfunction Involving MAPK Activation

机译:通过反应性氧物种介导的线粒体功能障碍诱导凋亡诱导涉及MAPK激活的电抗性的线粒体功能障碍

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Arachniodes exilisis used as a folk medicine in China and proved to have antibacterial, anti-inflammatory, and sedative activities. In the present study, the antitumor effect of the total flavonoids ofA. exilis(TFAE) against HepG2 cells was evaluated. The results showed that TFAE inhibited the growth of HepG2 cells in a dosage- and time-dependent manner. Flow cytometry and Hoechst 33342 fluorescence staining results showed that TFAE could significantly increase the apoptosis ratio of HepG2 cells, which is accompanied with increased intracellular reactive oxygen species (ROS) production and decreased mitochondrial membrane potential(ΔΨm). Western blotting indicated that TFAE downregulated the ratio of Bcl-2/Bax, increased cytochrome c release, and activated the caspases-3 and -9. Further analysis showed that TFAE stimulated the mitogen-activated protein kinase (MAPK). However, treatment with NAC (reactive oxygen species scavenger) and MAPK-specific inhibitors (SP600125 and SB203580) could reverse the changes of these apoptotic-related proteins. These results suggested that TFAE possessed potential anticancer activity in HepG2 cells through ROS-mediated mitochondrial dysfunction involving MAPK pathway.
机译:Arachniodes Exilisis被用作中国的民间医学,并证明具有抗菌,抗炎和镇静活动。在本研究中,抗肿瘤效应的总类黄酮。评估Exilis(TFAE)对抗HepG2细胞。结果表明,TFAE以剂量和时间依赖性方式抑制HepG2细胞的生长。流式细胞术和Hoechst 33342荧光染色结果表明,TFAE可以显着提高HepG2细胞的凋亡比,其伴随着增加的细胞内反应性氧(ROS)产生和线粒体膜电位(Δψm)。蛋白质印迹表明,TFAE下调了Bcl-2 / Bax,增加细胞色素C释放的比例,并活化了Caspases-3和-9。进一步的分析表明,TFAE刺激了丝裂原激活的蛋白激酶(MAPK)。然而,用NAC(反应性氧物质清除剂)和MAPK特异性抑制剂(SP600125和SB203580)的处理可以逆转这些凋亡相关蛋白质的变化。这些结果表明,TFAE通过涉及Mapk途径的ROS介导的线粒体功能障碍在HepG2细胞中具有潜在的抗癌活性。

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