首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >A profile of 8-oxo-dGTPase activities in the NCI-60 human cancer panel: Meta-analytic insight into the regulation and role of MTH1 (NUDT1) gene expression in carcinogenesis
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A profile of 8-oxo-dGTPase activities in the NCI-60 human cancer panel: Meta-analytic insight into the regulation and role of MTH1 (NUDT1) gene expression in carcinogenesis

机译:NCI-60人癌组的8氧代DGTPase活性的概况:Meta-Inalytic Insight进入MTH1(NUDT1)基因表达在致癌中的调节和作用

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摘要

We measured the specific 8-oxo-dGTPase activity profile of the NCI-60 panel of malignant cell lines, and MTH1 protein levels in a subset of 16 lines. Their 8-oxo-dGTPase activity was compared to twelve publicly accessible MTH1 mRNA expression data bases and their cross-consistency was analyzed. 8-oxo-dGTPase and MTH1 protein levels in these cell lines are generally, but not always, mainly determined by MTH1 mRNA expression levels. The aneuploidy number of MTH1 gene copies only slightly affects its mRNA expression levels. By using the data mining platforms Compare and CellMiner, our 8-oxo-dGTPase profile was compared to five global gene expression datasets to identify genes whose expression levels are directly or inversely associated with 8-oxo-dGTPase. We analyzed effects of SNP within MTH1 on MTH1 mRNA level and enzyme activity. Similar association analysis was performed for five microRNA expression datasets. We identified several proteins and microRNA which might be involved in the regulation of MTH1 expression and we discuss potential mechanisms. Comparison of chemical and natural products sensitivities of the NCI-60 panel suggests seven compounds which are directly or inversely associated with 8-oxo-dGTPase. We provide an integrated picture of MTH1 expression combined from eleven consistent MTH1 mRNA and our 8-oxo-dGTPase activity NCI-60 profiles.
机译:我们测量了NCI-60恶性细胞系的特异性8-氧代-DGPA酶活性,并且在16条线的子集中的MTH1蛋白水平。将其8-氧代-DGTPAse活性与12个公共可接近的MTH1 mRNA表达数据碱基进行比较,分析其交叉一致性。这些细胞系中的8-氧代-DGTPAse和MTH1蛋白水平通常,但并不总是由MTH1 mRNA表达水平决定。短倍性的MTH1基因拷贝的数量仅略微影响其mRNA表达水平。通过使用数据挖掘平台进行比较和Cellminer,将8-氧代-DGPA酶谱进行比较,与五个全局基因表达数据集进行比较,以鉴定其表达水平直接或与8-氧代DGPTP酶相关的基因。我们分析了在MTH1中的SNP对MTH1 mRNA水平和酶活性的影响。对五个MicroRNA表达数据集进行了类似的关联分析。我们鉴定了几种蛋白质和微小RNA,其可能参与MTH1表达的调节,并讨论潜在机制。 NCI-60面板的化学和天然产品的比较表明,七​​种化合物直接或与8-氧代DGTP酶直接相关。我们提供从11个一致的MTH1 mRNA和我们的8氧代-DGPA酶活性NCI-60型材组合的MTH1表达的集成图片。

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