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首页> 外文期刊>Probiotics and Antimicrobial Proteins >Apoptotic Effect of Saccharomyces cerevisiae on Human Colon Cancer SW480 Cells by Regulation of Akt/NF-& x138;B Signaling Pathway
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Apoptotic Effect of Saccharomyces cerevisiae on Human Colon Cancer SW480 Cells by Regulation of Akt/NF-& x138;B Signaling Pathway

机译:Akt / NF-&x138调节酿酒酵母酿酒酵母对人结肠癌SW480细胞的凋亡作用; B信号通路

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摘要

Drug resistance is one of the major problems, which causes recurrence of cancers. Therefore, complementary treatments are needed to improve the impacts of chemotherapy agents. The effect of probiotics as cancer-preventing agents through involvement in the activation of apoptotic pathways has been established. The present study sought to investigate how the heat-killed form of Saccharomyces cerevisiae (as a probiotic) could affect the Akt/NF-kB-induced apoptosis in colon cancer cells, the SW480 cell line. The cytotoxic effects of heat-killed yeast (HKY) and 5-fluorouracil (5-FU, as a positive control drug) were assayed using the MTT method. Morphological changes followed by apoptosis were examined using DAPI staining. The transcription and translation level of apoptosis genes were explored with qRT-PCR and western blotting. The data were analyzed using GraphPad Prism V6.0 Software. The results showed that HKY could induce apoptosis in colon cancer cell line through downregulation of p-Akt1, Rel A, Bcl-XL, pro-caspase 3, and pro-caspase 9 expressions, and upregulation of BAX, cleaved caspase-3, and cleaved caspase-9. Besides, Akt protein expression was not affected. It is noticeable that HKY had a better modulating effect on BAX expression compared with 5-FU. It was able to modulate Akt/NF-kB signaling pathway followed by the apoptotic cascade.
机译:耐药性是主要问题之一,导致癌症复发。因此,需要补充处理来改善化疗剂的影响。已经建立了益生菌作为癌症通过参与激活凋亡途径的患者的影响。本研究试图研究酿酒酵母的热杀死形式(作为益生菌)的酵母杀死的形式如何影响结肠癌细胞中的AKT / NF-KB诱导的细胞凋亡,SW480细胞系。使用MTT方法测定热杀死酵母(HKY)和5-氟尿嘧啶(5-FU,作为阳性对照药物)的细胞毒性作用。使用DAPI染色检查细胞凋亡的形态学变化。用QRT-PCR和Western印迹探索了凋亡基因的转录和翻译水平。使用GraphPad Prism V6.0软件进行分析数据。结果表明,通过P-AKT1,Rel A,Bcl-XL,Pro-Caspase 3和Pro-Caspase 9表达的下调,HKY可以在结肠癌细胞系中诱导结肠癌细胞凋亡,并且裂解裂解胱天冬酶-3的上调,以及切割的caspase-9。此外,AKT蛋白表达不受影响。与5-FU相比,HKY对BAX表达具有更好的调节作用是明显的。它能够调节AKT / NF-KB信号传导途径,然后调节凋亡级联。

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