Literature DB >> 16399373

Animal models of xenobiotic receptors in drug metabolism and diseases.

Haibiao Gong1, Michael W Sinz, Yan Feng, Taosheng Chen, Raman Venkataramanan, Wen Xie.   

Abstract

Drug-metabolizing enzymes, including phase II conjugating enzymes, play an important role in both drug metabolism and human diseases. The genes that encode these enzymes and transporters are inducible by numerous xenobiotics and endobiotics and the inducibility shows clear species specificity. In the past several years, orphan nuclear receptors, such as PXR and CAR, have been established as species-specific "xenobiotic receptors" that regulate the expression of phase I and phase II enzymes and drug transporters. The creation of xenobiotic receptor transgenic and knockout mice has not only provided an opportunity to dissect the transcriptional control of drug metabolizing enzymes, but also offered a unique opportunity to study the xenobiotic receptor-mediated enzyme regulation in both drug metabolism and diseases. "Humanized" hPXR transgenic mice represent a major step forward in the creation and utilization of humanized rodent models for toxicological assessment that may aid in the development of safer drugs.

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Year:  2005        PMID: 16399373     DOI: 10.1016/S0076-6879(05)00034-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  12 in total

Review 1.  Overcoming drug resistance by regulating nuclear receptors.

Authors:  Taosheng Chen
Journal:  Adv Drug Deliv Rev       Date:  2010-08-04       Impact factor: 15.470

Review 2.  Nonviral gene transfer as a tool for studying transcription regulation of xenobiotic metabolizing enzymes.

Authors:  Barbara Bonamassa; Dexi Liu
Journal:  Adv Drug Deliv Rev       Date:  2010-08-14       Impact factor: 15.470

3.  A vinblastine fluorescent probe for pregnane X receptor in a time-resolved fluorescence resonance energy transfer assay.

Authors:  Wenwei Lin; Taosheng Chen
Journal:  Anal Biochem       Date:  2013-09-14       Impact factor: 3.365

4.  Cyclin-dependent kinase 2 negatively regulates human pregnane X receptor-mediated CYP3A4 gene expression in HepG2 liver carcinoma cells.

Authors:  Wenwei Lin; Jing Wu; Hanqing Dong; David Bouck; Fu-Yue Zeng; Taosheng Chen
Journal:  J Biol Chem       Date:  2008-09-09       Impact factor: 5.157

5.  Oxazaphosphorine bioactivation and detoxification The role of xenobiotic receptors.

Authors:  Duan Wang; Hongbing Wang
Journal:  Acta Pharm Sin B       Date:  2012-04-01       Impact factor: 11.413

6.  Use of transgenic mice in UDP-glucuronosyltransferase (UGT) studies.

Authors:  Zhimin Ou; Min Huang; Lizi Zhao; Wen Xie
Journal:  Drug Metab Rev       Date:  2010-02       Impact factor: 4.518

Review 7.  PXR: a xenobiotic receptor of diverse function implicated in pharmacogenetics.

Authors:  Bin Zhang; Wen Xie; Matthew D Krasowski
Journal:  Pharmacogenomics       Date:  2008-11       Impact factor: 2.533

Review 8.  Using TR-FRET to Investigate Protein-Protein Interactions: A Case Study of PXR-Coregulator Interaction.

Authors:  Wenwei Lin; Taosheng Chen
Journal:  Adv Protein Chem Struct Biol       Date:  2017-08-31       Impact factor: 3.507

9.  Flavonoids activate pregnane x receptor-mediated CYP3A4 gene expression by inhibiting cyclin-dependent kinases in HepG2 liver carcinoma cells.

Authors:  Hanqing Dong; Wenwei Lin; Jing Wu; Taosheng Chen
Journal:  BMC Biochem       Date:  2010-06-16       Impact factor: 4.059

10.  Development of BODIPY FL vindoline as a novel and high-affinity pregnane X receptor fluorescent probe.

Authors:  Wenwei Lin; Jiuyu Liu; Cynthia Jeffries; Lei Yang; Yan Lu; Richard E Lee; Taosheng Chen
Journal:  Bioconjug Chem       Date:  2014-08-18       Impact factor: 4.774

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