Cytochrome P450 and xenobiotic receptor humanized mice

被引:108
作者
Gonzalez, FJ [1 ]
Yu, AM
机构
[1] NCI, Lab Metab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] SUNY Buffalo, Dept Pharmaceut Sci, Buffalo, NY 14260 USA
关键词
CYP; nuclear receptor; transgenic mouse model; drug metabolism; pharmacokinetics; pharmacogenetics; cancer; toxicity; ligands; gene activation;
D O I
10.1146/annurev.pharmtox.45.120403.100007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Most xenobiotics that enter the body are subjected to metabolism that functions primarily to facilitate their elimination. Metabolism of certain xenobiotics can also result in the production of electrophilic derivatives that can cause cell toxicity and transformation. Many xenobiotics can also activate receptors that in turn induce the expression of genes encoding xenobiotic-metabolizing enzymes and xenobiotic transporters. However, there are marked species differences in the way mammals respond to xenobiotics, which are due in large part to molecular differences in receptors and xenobiotic-metabolizing enzymes. This presents a problem in extrapolating data obtained with rodent model systems to humans. There are also polymorphisms in xenobiotic-metabolizing enzymes that can impact drug therapy and cancer susceptibility. In an effort to generate more reliable in vivo systems to study and predict human response to xenobiotics, humanized mice are under development.
引用
收藏
页码:41 / 64
页数:30
相关论文
共 142 条
[141]   A Cyp1a2-luciferase transgenic CD-1 mouse model:: Responses to aryl hydrocarbons similar to the humanized AhR mice [J].
Zhang, WS ;
Moorthy, B ;
Chen, M ;
Muthiah, K ;
Coffee, R ;
Purchio, AF ;
West, DB .
TOXICOLOGICAL SCIENCES, 2004, 82 (01) :297-307
[142]   A transgenic mouse model with a luciferase reporter for studying in vivo transcriptional regulation of the human CYP3A4 gene [J].
Zhang, WS ;
Purchio, AF ;
Chen, K ;
Wu, JM ;
Lu, L ;
Coffee, R ;
Contag, PR ;
West, DB .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (08) :1054-1064