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首页> 外文期刊>Biochemistry (Moscow). Supplement, Series B. Biomedical chemistry >Molecular mechanisms of antitumor activity of the polymeric form of niclosamide with respect to human colorectal cancer cells
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Molecular mechanisms of antitumor activity of the polymeric form of niclosamide with respect to human colorectal cancer cells

机译:Niclosamide相对于人结肠癌细胞的聚合物形式的抗肿瘤活性的分子机制

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Abstract Using poly(lactic-co-glycolic) acid a polymeric form of niclosamide (PFN) has been developed and its antitumor activity against human colorectal cancer cell lines SW837, Caco-2, COLO 320 HSR has been investigated in comparison with free niclosamide. PFN was shown to be more cytotoxic against cancer cells and less cytotoxic against normal cells (human embryonic lung fibroblasts) as compared to niclosamide. Free niclosamide and PFN share a common mechanism of the cytotoxic action on tumor cells, which is associated with mitochondrial damage (evaluated as a decrease in rhodamine 123 accumulation), and increased levels of reactive oxygen species, particularly mitochondrial superoxide anion, causing oxidative damage of intracellular targets. The action of niclosamide and PFN was accompanied by G0/G1 cell cycle arrest.]]>
机译:<![CDATA [<标题>摘要 ara>使用聚(乳酸二乙醇酸)酸的一种聚合物形式的Niclosamide(PFN)及其对人结肠直肠癌细胞系SW837,Caco的抗肿瘤活性 -2,与游离Niclosamide相比,已经研究了Colo 320 HSR。 与Niclosamide相比,PFN被证明对癌细胞的抗癌细胞毒性和对正常细胞(人胚胎肺成纤维细胞)的细胞毒性更少。 自由Niclosamide和PFN在肿瘤细胞上分享细胞毒性作用的常见机制,其与线粒体损伤有关(评价为罗丹明123积累的减少),以及增加的活性氧物质,特别是线粒体超氧化物阴离子的水平,导致氧化损伤 细胞内靶标。 Niclosamide和PFN的作用伴随着G <下标> 0 / g <下标> 1 细胞周期骤停。]>

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