首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Ganoderma Lucidum Polysaccharides Target a Fas/Caspase Dependent Pathway to Induce Apoptosis in Human Colon Cancer Cells
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Ganoderma Lucidum Polysaccharides Target a Fas/Caspase Dependent Pathway to Induce Apoptosis in Human Colon Cancer Cells

机译:灵芝灵芝多糖靶向Fas /胱天蛋白酶依赖性途径来诱导人结肠癌细胞凋亡。

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Ganoderma lucidum polysaccharides (GLP) extracted from Ganoderma lucidum have been shown to inducecell death in some kinds of cancer cells. This study investigated the cytotoxic and apoptotic effect of GLP onHCT-116 human colon cancer cells and the molecular mechanisms involved. Cell proliferation, cell migration,lactate dehydrogenase (LDH) levels and intracellular free calcium levels ([Ca2+]i) were determined by MTT,wound-healing, LDH release and fluorescence assays, respectively. Cell apoptosis was observed by scanningand transmission electron microscopy. For the mechanism studies, caspase-8 activation, and Fas and caspase-3expression were evaluated. Treatment of HCT-116 cells with various concentrations of GLP (0.625-5 mg/mL)resulted in a significant decrease in cell viability (P< 0.01). This study showed that the antitumor activity ofGLP was related to cell migration inhibition, cell morphology changes, intracellular Ca2+ elevation and LDHrelease. Also, increase in the levels of caspase-8 activity was involved in GLP-induced apoptosis. Western blottingindicated that Fas and caspase-3 protein expression was up-regulated after exposure to GLP. This investigationdemonstrated for the first time that GLP shows prominent anticancer activities against the HCT-116 humancolon cancer cell line through triggering intracellular calcium release and the death receptor pathway.
机译:从灵芝提取的灵芝多糖(GLP)已显示在某些类型的癌细胞中诱导细胞死亡。这项研究调查了GLP对HCT-116人结肠癌细胞的细胞毒性和凋亡作用及其所涉及的分子机制。通过MTT,伤口愈合,LDH释放和荧光测定分别测定细胞增殖,细胞迁移,乳酸脱氢酶(LDH)水平和细胞内游离钙水平([Ca2 +] i)。通过扫描和透射电镜观察细胞凋亡。对于机制研究,评估了caspase-8激活,Fas和caspase-3的表达。用各种浓度的GLP(0.625-5 mg / mL)处理HCT-116细胞会导致细胞活力显着降低(P <0.01)。这项研究表明,GLP的抗肿瘤活性与细胞迁移抑制,细胞形态变化,细胞内Ca2 +升高和LDH释放有关。同样,caspase-8活性水平的升高也参与了GLP诱导的细胞凋亡。 Western blotting提示,暴露于GLP后Fas和caspase-3蛋白表达上调。这项研究首次证明,GLP通过触发细胞内钙释放和死亡受体途径,对HCT-116人结肠癌细胞系显示出显着的抗癌活性。

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