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Chemical Characterization and Antitumor Activities of Polysaccharide Extracted from Ganoderma lucidum

机译:灵芝多糖的化学表征及抗肿瘤活性

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Ganoderma lucidum polysaccharide (GLP) is a biologically active substance reported to possess anti-tumor ability. Nonetheless, the mechanisms of GLP-stimulated apoptosis are still unclear. This study aims to determine the inhibitory and apoptosis-inducing effects of GLP on HCT-116 cells. We found that GLP reduced cell viability on HCT-116 cells in a time- and dose-dependent manner, which in turn, induced cell apoptosis. The observed apoptosis was characterized by morphological changes, DNA fragmentation, mitochondrial membrane potential decrease, S phase population increase, and caspase-3 and -9 activation. Furthermore, inhibition of c-Jun N-terminal kinase (JNK) by SP600125 led to a dramatic decrease of the GLP-induced apoptosis. Western blot analysis unveiled that GLP up-regulated the expression of Bax/Bcl-2, caspase-3 and poly (ADP-ribose) polymerase (PARP). These results demonstrate that apoptosis stimulated by GLP in human colorectal cancer cells is associated with activation of mitochondrial and mitogen-activated protein kinase (MAPK) pathways.
机译:灵芝多糖(GLP)是据报道具有抗肿瘤能力的生物活性物质。尽管如此,GLP刺激的细胞凋亡的机制仍不清楚。这项研究旨在确定GLP对HCT-116细胞的抑制和凋亡诱导作用。我们发现,GLP以时间和剂量依赖性方式降低了HCT-116细胞的细胞活力,进而诱导了细胞凋亡。观察到的细胞凋亡的特征是形态变化,DNA片段化,线粒体膜电位降低,S期群体增加以及caspase-3和-9激活。此外,SP600125对c-Jun N末端激酶(JNK)的抑制作用导致GLP诱导的细胞凋亡显着减少。蛋白质印迹分析揭示了GLP上调了Bax / Bcl-2,caspase-3和聚(ADP-核糖)聚合酶(PARP)的表达。这些结果表明,人结肠直肠癌细胞中GLP刺激的细胞凋亡与线粒体和丝裂原激活的蛋白激酶(MAPK)途径的激活有关。

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