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首页> 外文期刊>International immunopharmacology >Ursolic acid induces apoptosis by activating p53 and caspase-3 gene expressions and suppressing NF-kappaB mediated activation of bcl-2 in B16F-10 melanoma cells.
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Ursolic acid induces apoptosis by activating p53 and caspase-3 gene expressions and suppressing NF-kappaB mediated activation of bcl-2 in B16F-10 melanoma cells.

机译:熊果酸通过激活p16和caspase-3基因表达并抑制NF-κB介导的B16F-10黑色素瘤细胞bcl-2的激活来诱导凋亡。

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The objective of this study was to assess the effect of ursolic acid, a triterpene on inducing apoptosis in B16F-10 melanoma cells. Treatment of B16F-10 cells with nontoxic concentration of ursolic acid showed the presence of apoptotic bodies and induced DNA fragmentation in a dose depended manner. The apoptotic genes p53 and caspase-3 were found to be upregulated while the anti-apoptotic gene bcl-2 was down regulated in ursolic acid treated cells. The transcription factors NF-kappaBp65, NF-kappaBp50, NF-kappaBc-Rel, c-FOS, ATF-2 and CREB-1 were found to be inhibited significantly (p<0.001) in ursolic acid treated cells compared to untreated control. The pro-inflammatory cytokine production and gene expression of TNF-alpha, IL-1beta, IL-6 and GM-CSF were down regulated in ursolic acid treated cells compared to nontreated B16F-10 metastatic melanoma cells. All these results demonstrate that ursolic acid induce apoptosis via inhibition of NF-kappaB induced bcl-2 mediated anti-apoptotic pathway and subsequent activation of p53 mediated and TNF-alpha induced caspase-3 mediated pro-apoptotic pathways.
机译:这项研究的目的是评估熊果酸,一种三萜对诱导B16F-10黑色素瘤细胞凋亡的作用。用无毒浓度的熊果酸处理B16F-10细胞显示凋亡小体的存在,并以剂量​​依赖的方式诱导DNA断裂。发现在熊果酸处理的细胞中,凋亡基因p53和caspase-3被上调,而抗凋亡基因bcl-2被下调。与未处理的对照相比,在熊果酸处理的细胞中发现转录因子NF-κBp65,NF-κBp50,NF-κBc-Rel,c-FOS,ATF-2和CREB-1被显着抑制(p <0.001)。与未处理的B16F-10转移性黑素瘤细胞相比,在熊果酸处理的细胞中促炎性细胞因子的产生和TNF-α,IL-1β,IL-6和GM-CSF的基因表达被下调。所有这些结果表明,熊果酸通过抑制NF-κB诱导的bcl-2介导的抗凋亡途径和随后激活p53介导的和TNF-α诱导的caspase-3介导的促凋亡途径来诱导凋亡。

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