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首页> 外文期刊>Biotechnology and Applied Biochemistry >Alteration of mitochondrial membrane potential by Spirulina platensis C-phycocyanin induces apoptosis in the doxorubicin-resistant human hepatocellular-carcinoma cell line HepG2
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Alteration of mitochondrial membrane potential by Spirulina platensis C-phycocyanin induces apoptosis in the doxorubicin-resistant human hepatocellular-carcinoma cell line HepG2

机译:螺旋藻C-藻蓝蛋白改变线粒体膜电位诱导抗阿霉素的人肝癌细胞HepG2凋亡

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摘要

C-PC (C-phycocyanin) is a water-soluble biliprotein from the filamentous cyanobacterium Spirulina platensis with potent antioxidant, anti-inflammatory and anticancerous properties. In the present study, the effect of C-PC was tested on the proliferation of doxorubicin-sensitive (S-HepG2) and -resistant (R-HepG2) HCC (hepatocellular carcinoma) cell lines. These studies indicate a 50% decrease in the proliferation of S- and R-HepG2 cells treated with 40 and SO mu M C-PC for 24 h respectively. C-PC also enhanced the sensitivity of R-HepG2 cells to doxorubicin. R-HepG2 cells treated with C-PC showed typical apoptotic features such as membrane blebbing and DNA fragmentation. Flow-cytometric analysis of R-HepG2 cells treated with 10, 25 and 50 mu M C-PC for 24 h showed 18.8, 39.72 and 65.64% cells in sub-G(0)/G(1)-phase respectively. Cytochrome c release, decrease in membrane potential, caspase 3 activation and PARP [poly(ADPribose) polymerase] cleavage were observed in CPC-treated R-HepG2 cells. These studies also showed down-regulation of the anti-apoptotic protein Bcl-2 and up-regulation of the pro-apoptotic Bax (Bcl2-associated X-protein) protein in the R-HepG2 cells treated with C-PC. The present study thus demonstrates that C-PC induces apoptosis in R-HepG2 cells and its potential as an anti-HCC agent.
机译:C-PC(C-藻蓝蛋白)是一种来自丝状蓝藻螺旋藻的水溶性胆蛋白,具有强大的抗氧化剂,抗炎和抗癌特性。在本研究中,测试了C-PC对阿霉素敏感性(S-HepG2)和耐药性(R-HepG2)HCC(肝细胞癌)细胞系增殖的影响。这些研究表明分别用40和SOμM C-PC处理24小时的S-和R-HepG2细胞的增殖减少了50%。 C-PC还增强了R-HepG2细胞对阿霉素的敏感性。经C-PC处理的R-HepG2细胞表现出典型的凋亡特征,例如膜起泡和DNA片段化。用10、25和50μM C-PC处理24小时的R-HepG2细胞的流式细胞仪分析显示,分别在sub-G(0)/ G(1)期中有18.8%,39.72%和65.64%的细胞。在CPC处理的R-HepG2细胞中观察到细胞色素c释放,膜电位降低,胱天蛋白酶3活化和PARP [poly(ADPribose)聚合酶]裂解。这些研究还显示,在用C-PC处理的R-HepG2细胞中,抗​​凋亡蛋白Bcl-2的下调和促凋亡Bax(Bcl2相关的X蛋白)蛋白的上调。因此,本研究证明C-PC诱导R-HepG2细胞凋亡,并具有作为抗HCC药物的潜力。

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