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Dramatic down-regulation of oxidoreductases in human hepatocellular carcinoma hepG2 cells: proteomics and gene ontology unveiling new frontiers in cancer enzymology

机译:人肝细胞癌HepG2细胞中氧化还原酶的急剧下调:蛋白质组学和基因本体论揭示了癌症酶学的新领域

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摘要

BackgroundOxidoreductases are enzymes that catalyze many redox reactions in normal and neoplastic cells. Their actions include catalysis of the transformation of free, neutral oxygen gas into oxygen free radicals, superoxide, hydroperoxide, singlet oxygen and hydrogen peroxide. These activated forms of oxygen contribute to oxidative stress that modifies lipids, proteins, DNA and carbohydrates. On the other hand, oxidoreductases constitute one of the most important free radical scavenger systems typified by catalase, superoxide dismutase and glutathione peroxidase.In this work, proteomics, Gene Ontology mapping and Directed Acyclic Graphs (DAG) are employed to detect and quantify differential oxidoreductase enzyme expressions between HepG2 cells and normal human liver tissues.
机译:背景氧化还原酶是催化正常和肿瘤细胞中许多氧化还原反应的酶。它们的作用包括催化将游离的中性氧气转化为氧自由基,超氧化物,氢过氧化物,单线态氧和过氧化氢。这些活化的氧气有助于氧化应激,从而改变脂质,蛋白质,DNA和碳水化合物。另一方面,氧化还原酶是最重要的自由基清除剂系统之一,以过氧化氢酶,超氧化物歧化酶和谷胱甘肽过氧化物酶为代表。在这项工作中,蛋白质组学,基因本体图谱和有向无环图(DAG)用于检测和定量差异氧化还原酶。 HepG2细胞与正常人肝组织之间的酶表达。

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