| Literature DB >> 28013219 |
Yan Jiang1,2, Jiahong Chen2,3, Cong Yue2,3, Hang Zhang2,3, Jian Tong2,3, Jianxiang Li2,3, Tao Chen2,3.
Abstract
Trichloroethylene (TCE), commonly used as an industrial solvent, is ubiquitous in our living environment. TCE exposure can induce hepatocellular carcinoma (HCC) in mice, but the underlying mechanisms remain elusive. To understand the role of miRNA in the hepatocarcinogenesis of TCE, we examined the miRNA expression profiles by microarray in the liver of B6C3F1 male mice exposed to TCE at 0 or 1000 mg/kg b.w. Nine differentially expressed miRNAs were identified, out of which miR-182-5p exhibited the highest increase in expression. Moreover, the TCE-induced upregulation of miR182-5p in mouse liver was dose dependent and correlated with promoter DNA hypomethylation. Treatment of mouse liver cell lines (BNL CL.2 and Hepa1-6) with TCE at non-toxic doses (0.1 and/or 0.3 mM) significantly increased the expression level of miR-182-5p accompanied with elevated cell proliferation. The TCE-induced cell proliferation was further found to be mediated by miR-182-5p overexpression. Additionally, tumor suppressor gene Cited2, which was downregulated in TCE exposed mouse liver cells, was proved to be a direct target of miR-182-5p. In conclusion, TCE might up-regulate miR-182-5p expression by DNA hypomethylation, which could suppress Cited2 and improve cell proliferation rate, resulting in liver tumor.Entities:
Keywords: trichloroethylene (TCE); miR-182-5p; DNA methylation; liver;zzm321990 mouse.
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Year: 2017 PMID: 28013219 DOI: 10.1093/toxsci/kfw246
Source DB: PubMed Journal: Toxicol Sci ISSN: 1096-0929 Impact factor: 4.849