PXR and CAR: Nuclear receptors which play a pivotal role in drug disposition and chemical toxicity

被引:111
|
作者
Stanley, Lesley A.
Horsburgh, Brian C.
Ross, Jillian
Scheer, Nico
Wolf, C. Roland
机构
[1] Investigat Toxicol, St Andrews, Fife, Scotland
[2] ITI Life Sci, Dundee, Scotland
[3] CXR Biosci, Dundee, Scotland
[4] Artemis Pharmaceut GmbH, Cologne, Germany
关键词
pregnane-X-receptor; constitutive androstane receptor; cytochrome P450; CYP2B; CYP3A; null mice; humanised mice; transcription factors;
D O I
10.1080/03602530600786232
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Xenobiotic metabolism and detoxification is regulated by receptors (e.g., PXR, CAR) whose characterization has contributed significantly to our understanding of drug responses in humans. Technologies facilitating the screening of compounds for receptor interactions provide valuable tools applicable in drug development. Most use in vitro systems or mice humanized for receptors in vivo. In vitro assays are limited by the reporter systems and cell lines chosen and are uninformative about effects in vivo. Humanized mouse models provide novel, exciting ways of understanding the functions of these genes. This article evaluates these technologies and current knowledge on PXR/CAR-mediated regulation of gene expression.
引用
收藏
页码:515 / 597
页数:83
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