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
[91]   A novel panel of mouse models to evaluate the role of human pregnane X receptor and constitutive androstane receptor in drug response [J].
Scheer, Nico ;
Ross, Jillian ;
Rode, Anja ;
Zevnik, Branko ;
Niehaves, Sandra ;
Faust, Nicole ;
Wolf, C. Roland .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (09) :3228-3239
[92]   Interplay between the Nuclear Receptor Pregnane X Receptor and the Uptake Transporter Organic Anion Transporter Polypeptide 1A2 Selectively Enhances Estrogen Effects in Breast Cancer [J].
Schwabedissen, Henriette E. Meyer Zu ;
Tirona, Rommel G. ;
Yip, Cindy S. ;
Ho, Richard H. ;
Kim, Richard B. .
CANCER RESEARCH, 2008, 68 (22) :9338-9347
[93]   Structure of the murine constitutive androstane receptor complexed to androstenol: A molecular basis for inverse agonism [J].
Shan, L ;
Vincent, J ;
Brunzelle, JS ;
Dussault, I ;
Lin, M ;
Ianculescu, I ;
Sherman, MA ;
Forman, BM ;
Fernandez, EJ .
MOLECULAR CELL, 2004, 16 (06) :907-917
[94]   Induction of rat UDP-glucuronosyltransferases in liver and duodenum by microsomal enzyme inducers that activate various transcriptional pathways [J].
Shelby, M. K. ;
Klaassen, C. D. .
DRUG METABOLISM AND DISPOSITION, 2006, 34 (10) :1772-1778
[95]   Dexamethasone transcriptionally increases the expression of the pregnane X receptor and synergistically enhances pyrethroid esfenvalerate in the induction of cytochrome P450 3A23 [J].
Shi, Deshi ;
Yang, Dongfang ;
Yan, Bingfang .
BIOCHEMICAL PHARMACOLOGY, 2010, 80 (08) :1274-1283
[96]   Cytochrome P450 7A1 Cholesterol 7α-Hydroxylation INDIVIDUAL REACTION STEPS IN THE CATALYTIC CYCLE AND RATE-LIMITING FERRIC IRON REDUCTION [J].
Shinkyo, Raku ;
Guengerich, F. Peter .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (06) :4632-4643
[97]   Identification of Clinically Used Drugs That Activate Pregnane X Receptors [J].
Shukla, Sunita J. ;
Sakamuru, Srilatha ;
Huang, Ruili ;
Moeller, Timothy A. ;
Shinn, Paul ;
VanLeer, Danielle ;
Auld, Douglas S. ;
Austin, Christopher P. ;
Xia, Menghang .
DRUG METABOLISM AND DISPOSITION, 2011, 39 (01) :151-159
[98]   Pharmacokinetics and pharmacodynamics of drug interactions involving rifampicin, rifabutin and antimalarial drugs [J].
Sousa, Marta ;
Pozniak, Anton ;
Boffito, Marta .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 62 (05) :872-878
[99]   Cytoplasmic localization of pregnane X receptor and ligand-dependent nuclear translocation in mouse liver [J].
Squires, EJ ;
Sueyoshi, T ;
Negishi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (47) :49307-49314
[100]  
Staudinger J, 2001, DRUG METAB DISPOS, V29, P1467