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Trichloroethylene-Induced Gene Expression and DNA Methylation Changes in B6C3F1 Mouse Liver

机译:三氯乙烯诱导的B6C3F1小鼠肝脏中的基因表达和DNA甲基化变化

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摘要

Trichloroethylene (TCE), widely used as an organic solvent in the industry, is a common contaminant in air, soil, and water. Chronic TCE exposure induced hepatocellular carcinoma in mice, and occupational exposure in humans was suggested to be associated with liver cancer. To understand the role of non-genotoxic mechanism(s) for TCE action, we examined the gene expression and DNA methylation changes in the liver of B6C3F1 mice orally administered with TCE (0, 100, 500 and 1000 mg/kg b.w. per day) for 5 days. After 5 days TCE treatment at a dose level of 1000 mg/kg b.w., a total of 431 differentially expressed genes were identified in mouse liver by microarray, of which 291 were up-regulated and 140 down-regulated. The expression changed genes were involved in key signal pathways including PPAR, proliferation, apoptosis and homologous recombination. Notably, the expression level of a number of vital genes involved in the regulation of DNA methylation, such as Utrf1, Tet2, DNMT1, DNMT3a and DNMT3b, were dysregulated. Although global DNA methylation change was not detected in the liver of mice exposed to TCE, the promoter regions of Cdkn1a and Ihh were found to be hypo- and hypermethylated respectively, which correlated negatively with their mRNA expression changes. Furthermore, the gene expression and DNA methylation changes induced by TCE were dose dependent. The overall data indicate that TCE exposure leads to aberrant DNA methylation changes, which might alter the expression of genes involved in the TCE-induced liver tumorgenesis.
机译:三氯乙烯(TCE)在工业中广泛用作有机溶剂,是空气,土壤和水中的常见污染物。长期TCE暴露引起小鼠肝细胞癌,人类职业暴露与肝癌有关。为了了解非遗传毒性机制对TCE作用的作用,我们检查了口服TCE(每天0、100、500和1000 mg / kg bw)的B6C3F1小鼠肝脏中的基因表达和DNA甲基化变化5天。在以1000 mg / kg b.w.的剂量水平进行5天的TCE处理后,通过微阵列在小鼠肝脏中鉴定出总共431个差异表达基因,其中291个上调而140个下调。表达改变的基因参与了关键信号途径,包括PPAR,增殖,凋亡和同源重组。值得注意的是,许多参与DNA甲基化调控的重要基因的表达水平失调。例如,Utrf1,Tet2,DNMT1,DNMT3a和DNMT3b。尽管在暴露于TCE的小鼠肝脏中未检测到总体DNA甲基化变化,但发现Cdkn1a和Ihh的启动子区域分别为低甲基化和高甲基化,与它们的mRNA表达变化呈负相关。此外,TCE诱导的基因表达和DNA甲基化变化是剂量依赖性的。总体数据表明,TCE暴露会导致异常的DNA甲基化变化,这可能会改变TCE诱导的肝肿瘤发生中涉及的基因表达。

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