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Research ArticleArticle

Regulation of Tissue-Specific Carboxylesterase Expression by Pregnane X Receptor and Constitutive Androstane Receptor

Chenshu Xu, Xinkun Wang and Jeff L. Staudinger
Drug Metabolism and Disposition July 2009, 37 (7) 1539-1547; DOI: https://doi.org/10.1124/dmd.109.026989
Chenshu Xu
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Xinkun Wang
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Jeff L. Staudinger
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Abstract

The liver- and intestine-enriched carboxylesterase 2 (CES2) enzyme catalyzes the hydrolysis of several clinically important anticancer agents administered as prodrugs. For example, irinotecan, a carbamate prodrug used in the treatment of colorectal cancer, is biotransformed in vivo by CES2 in intestine and liver, thereby producing a potent topoisomerase I inhibitor. Pregnane X receptor (PXR) and constitutive androstane receptor (CAR), two members of the nuclear receptor superfamily of ligand-activated transcription factors, mediate gene activation in response to xenobiotic stress. Together, these receptors comprise a protective response in mammals that coordinately regulate hepatic transport, metabolism, and elimination of numerous xenobiotic compounds. In the present study, microarray analysis was used to identify PXR target genes in duodenum in mice. Here, we show that a gene encoding a member of the CES2 subtype of liver- and intestine-enriched CES enzymes, called Ces6, is induced after treatment with pregnenolone 16α-carbonitrile in a PXR-dependent manner in duodenum and liver in mice. Treatment of mice with the CAR activator 1,4-bis[2-(3,5-dichloropyridyloxy)] benzene also induced expression of Ces6 in duodenum and liver in a CAR-dependent manner, whereas treatment with phenobarbital produced induction of Ces6 exclusively in liver. These data identify a key role for PXR and CAR in regulating the drug-inducible expression and activity of an important CES enzyme in vivo. Future studies should focus on determining whether these signaling pathways governing drug-inducible CES expression in intestine and liver are conserved in humans.

Footnotes

  • This work was supported by the National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases [Grant DK068443].

  • Article, publication date, and citation information can be found at http://dmd.aspetjournals.org.

  • doi:10.1124/dmd.109.026989.

  • ABBREVIATIONS: CES, carboxylesterase; PXR, pregnane X receptor; CAR, constitutive androstane receptor; PB, phenobarbital; PCN, pregnenolone 16α-carbonitrile; PXR-KO, PXR knockout; CAR-KO, CAR knockout; TCPOBOP, 1,4-bis[2-(3,5-dichloropyridyloxy)] benzene; QC, quality control; rt-QPCR, real-time quantitative polymerase chain reaction; PPAR, peroxisome proliferator-activated receptor.

    • Accepted April 8, 2009.
    • Received January 30, 2009.
  • The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 37 (7)
Drug Metabolism and Disposition
Vol. 37, Issue 7
1 Jul 2009
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Research ArticleArticle

Regulation of Tissue-Specific Carboxylesterase Expression by Pregnane X Receptor and Constitutive Androstane Receptor

Chenshu Xu, Xinkun Wang and Jeff L. Staudinger
Drug Metabolism and Disposition July 1, 2009, 37 (7) 1539-1547; DOI: https://doi.org/10.1124/dmd.109.026989

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Research ArticleArticle

Regulation of Tissue-Specific Carboxylesterase Expression by Pregnane X Receptor and Constitutive Androstane Receptor

Chenshu Xu, Xinkun Wang and Jeff L. Staudinger
Drug Metabolism and Disposition July 1, 2009, 37 (7) 1539-1547; DOI: https://doi.org/10.1124/dmd.109.026989
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