Downregulation of cytochrome P450 2C8 by 3-methylcholanthrene in human hepatocellular carcinoma cell lines

被引:2
作者
Utgikar, Rucha [1 ]
Riddick, David S. [1 ]
机构
[1] Univ Toronto, Dept Pharmacol & Toxicol, Med Sci Bldg, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
cytochrome P450; CYP2C8; drug metabolism; polycyclic aromatic hydrocarbons; 3-methylcholanthrene; HepG2; cells; HepaRG cells; aryl hydrocarbon receptor; POLYCYCLIC AROMATIC-HYDROCARBONS; PRIMARY HUMAN HEPATOCYTES; HUMAN CYP2C8; HUMAN LIVER; TRANSCRIPTIONAL REGULATION; GENE-EXPRESSION; INDUCTION; SUPPRESSION; P4502C11; RECEPTOR;
D O I
10.1139/cjpp-2017-0014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The marked induction of cytochromes P450 such as CYP1A1 caused by polycyclic aromatic hydrocarbons (PAHs) like 3-methylcholanthrene (MC) is often accompanied by suppression of other hepatic P450s. The molecular mechanisms, functional consequences, and human relevance of P450 downregulation by PAHs are poorly understood. MC suppresses mRNA levels for CYP2C8, an important human P450, in cultured human hepatocytes. To avoid hepatocyte lot-to-lot variability, we assessed CYP2C8 regulation by MC in HepaRG cells, a terminally differentiated human hepatocellular carcinoma cell line that maintains high P450 expression. MC strongly induced CYP1A1 mRNA levels and markedly downregulated CYP2C8 mRNA levels in HepaRG cells. Although MC also suppressed CYP2C8 mRNA levels in the HepG2 human hepatocellular carcinoma cell line, basal CYP2C8 expression was extremely low. HepaRG cells appear to be an appropriate model system for studying the mechanisms and functional consequences of CYP2C8 downregulation by PAHs.
引用
收藏
页码:768 / 771
页数:4
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