Role of CAR and PXR in xenobiotic sensing and metabolism

被引:199
作者
Wang, Yue-Ming [1 ]
Ong, Su Sien [1 ]
Chai, Sergio C. [1 ]
Chen, Taosheng
机构
[1] St Jude Childrens Res Hosp, Dept Chem Biol & Therapeut, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
constitutive androstane receptor; drug-drug interactions; pregnane X receptor; xenobiotic detoxification; PREGNANE-X-RECEPTOR; CONSTITUTIVE ANDROSTANE RECEPTOR; ORPHAN NUCLEAR RECEPTOR; CYP3A4; GENE-EXPRESSION; DRUG-INTERACTIONS; STRUCTURAL DETERMINANTS; DIFFERENTIAL REGULATION; ACTIVATED RECEPTOR; INTESTINAL MDR1; MOLECULAR-BASIS;
D O I
10.1517/17425255.2012.685237
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: The xenobiotic detoxification system, which protects the human body from external chemicals, comprises drug-metabolizing enzymes and transporters whose expressions are regulated by pregnane X receptor (PXR) and the constitutive androstane receptor (CAR). The progress made in a large number of recent studies calls for a timely review to summarize and highlight these key discoveries. Areas covered: This review summarizes recent advances in elucidating the roles of PXR and CAR in the xenobiotic detoxification system. It also highlights the progress in understanding the regulation of PXR and CAR activity at the post-translational levels, as well as the structural basis for the regulation of these two xenobiotic sensors. Expert opinion: Future efforts are needed to discover novel agonists and antagonists with species and isoform selectivity, to systematically understand the regulation of PXR and CAR at multiple levels (transcriptional, post-transcriptional and post-translational levels) in response to xenobiotics exposure, and to solve the structures of the full-length receptors, which will be enabled by improved protein expression and purification techniques and approaches. In addition, more efforts will be needed to validate PXR and CAR as disease-related therapeutic targets and thus expand their roles as master xenobiotic sensors.
引用
收藏
页码:803 / 817
页数:15
相关论文
共 134 条
[11]   Overcoming drug resistance by regulating nuclear receptors [J].
Chen, Taosheng .
ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (13) :1257-1264
[12]   Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter [J].
Chen, YP ;
Ferguson, SS ;
Negishi, M ;
Goldstein, JA .
MOLECULAR PHARMACOLOGY, 2003, 64 (02) :316-324
[13]   Induction of human CYP2C9 by rifampicin, hyperforin, and phenobarbital is mediated by the pregnane X receptor [J].
Chen, YP ;
Ferguson, SS ;
Negishi, M ;
Goldstein, JA .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 308 (02) :495-501
[14]   ChIPing the cistrome of PXR in mouse liver [J].
Cui, Julia Yue ;
Gunewardena, Sumedha S. ;
Rockwell, Cheryl E. ;
Klaassen, Curtis D. .
NUCLEIC ACIDS RESEARCH, 2010, 38 (22) :7943-7963
[15]   Induction of metabolism and transport in human intestine: Validation of precision-cut slices as a tool to study induction of drug metabolism in human intestine in vitro [J].
De Kerkhof, Esther G. Van ;
De Graaf, Inge A. M. ;
Ungell, Anna-Lena B. ;
Groothuis, Geny M. M. .
DRUG METABOLISM AND DISPOSITION, 2008, 36 (03) :604-613
[16]   Nuclear receptors CAR and PXR: Molecular, functional, and biomedical aspects [J].
di Masi, Alessandra ;
De Marinis, Elisabetta ;
Ascenzi, Paolo ;
Marino, Maria .
MOLECULAR ASPECTS OF MEDICINE, 2009, 30 (05) :297-343
[17]   Induction of drug metabolism by forskolin: The role of the pregnane X receptor and the protein kinase A signal transduction pathway [J].
Ding, XS ;
Staudinger, JL .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 312 (02) :849-856
[18]   Flavonoids activate activate pregnane x receptor-mediated CYP3A4 gene expression by inhibiting cyclin-dependent kinases in HepG2 liver carcinoma cells [J].
Dong, Hanqing ;
Lin, Wenwei ;
Wu, Jing ;
Chen, Taosheng .
BMC BIOCHEMISTRY, 2010, 11
[19]   Rational quantitative structure-activity relationship (RQSAR) screen for PXR and CAR isoform-specific nuclear receptor ligands [J].
Dring, Ann M. ;
Anderson, Linnea E. ;
Qamar, Saima ;
Stoner, Matthew A. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2010, 188 (03) :512-525
[20]   A ligand-based approach to understanding selectivity of nuclear hormone receptors PXR, CAR, FXR, LXRα, and LXRβ [J].
Ekins, S ;
Mirny, L ;
Schuetz, EG .
PHARMACEUTICAL RESEARCH, 2002, 19 (12) :1788-1800