Similarities and Differences in the Expression of Drug-Metabolizing Enzymes between Human Hepatic Cell Lines and Primary Human Hepatocytes

被引:267
作者
Guo, Lei [2 ]
Dial, Stacey [3 ]
Shi, Leming [4 ]
Branham, William [4 ]
Liu, Jie [1 ]
Fang, Jia-Long [2 ]
Green, Bridgett [1 ]
Deng, Helen [5 ]
Kaput, Jim [1 ]
Ning, Baitang [1 ]
机构
[1] US FDA, Div Personalized Nutr & Med, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[2] US FDA, Div Biochem Toxicol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[3] US FDA, Div Genet & Reprod Toxicol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[4] US FDA, Div Syst Biol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[5] Arkansas Dept Hlth, Little Rock, AR 72205 USA
基金
美国国家卫生研究院;
关键词
HUMAN-LIVER; CYTOCHROME-P450; ENZYMES; TRANSCRIPTION FACTORS; HEPG2; CELLS; GENE; INDUCTION; DIFFERENTIATION; TOXICITY; INHIBITION; CLEARANCE;
D O I
10.1124/dmd.110.035873
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In addition to primary human hepatocytes, hepatoma cell lines, and transfected nonhepatoma, hepatic cell lines have been used for pharmacological and toxicological studies. However, a systematic evaluation and a general report of the gene expression spectra of drug-metabolizing enzymes and transporters (DMETs) in these in vitro systems are not currently available. To fill this information gap and to provide references for future studies, we systematically characterized the basal gene expression profiles of 251 drug-metabolizing enzymes in untreated primary human hepatocytes from six donors, four commonly used hepatoma cell lines (HepG2, Huh7, SK-Hep-1, and Hep3B), and one transfected human liver epithelial cell line. A large variation in DMET expression spectra was observed between hepatic cell lines and primary hepatocytes, with the complete absence or much lower abundance of certain DMETs in hepatic cell lines. Furthermore, the basal DMET expression spectra of five hepatic cell lines are summarized, providing references for researchers to choose carefully appropriate in vitro models for their studies of drug metabolism and toxicity, especially for studies with drugs in which toxicities are mediated through the formation of reactive metabolites.
引用
收藏
页码:528 / 538
页数:11
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