Literature DB >> 2693891

Induction of hepatic cytochrome P450 gene expression by 2,3,7,8-tetrachlorodibenzo-p-dioxin.

J P Whitlock1, M S Denison, J M Fisher, E S Shen.   

Abstract

The halogenated aromatic hydrocarbon 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, dioxin) is a persistent, widespread, potentially toxic environmental contaminant, which is a potent inducer of aryl hydrocarbon hydroxylase activity in the liver and other tissues. TCDD induces hydroxylase activity by increasing the rate of transcription of the CYP1A1 gene. Activation of CYP1A1 transcription requires the binding of TCDD to an intracellular protein, the Ah receptor, followed by the binding of the liganded receptor to a dioxin-responsive enhancer that is located upstream from the CYP1A1 gene. The liganded receptor recognizes a specific DNA sequence, which is present in multiple copies within the enhancer. The receptor-enhancer interaction occurs within the major groove of the DNA helix. DNA methylation in vitro interferes with the receptor-enhancer interaction and, therefore, has the potential to inhibit the biological response to TCDD.

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Year:  1989        PMID: 2693891

Source DB:  PubMed          Journal:  Mol Biol Med        ISSN: 0735-1313


  9 in total

Review 1.  The Ah receptor and the mechanism of dioxin toxicity.

Authors:  J P Landers; N J Bunce
Journal:  Biochem J       Date:  1991-06-01       Impact factor: 3.857

2.  Functional antioxidant responsive elements.

Authors:  W W Wasserman; W E Fahl
Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-13       Impact factor: 11.205

3.  Identification and characterization of genes susceptible to transcriptional cross-talk between the hypoxia and dioxin signaling cascades.

Authors:  KangAe Lee; Lyle D Burgoon; Laura Lamb; Edward Dere; Timothy R Zacharewski; John B Hogenesch; John J LaPres
Journal:  Chem Res Toxicol       Date:  2006-10       Impact factor: 3.739

4.  Coordinated regulation of hepatic phase I and II drug-metabolizing genes and transporters using AhR-, CAR-, PXR-, PPARα-, and Nrf2-null mice.

Authors:  Lauren M Aleksunes; Curtis D Klaassen
Journal:  Drug Metab Dispos       Date:  2012-04-11       Impact factor: 3.922

5.  Inhibition of constitutive aryl hydrocarbon receptor (AhR) signaling attenuates androgen independent signaling and growth in (C4-2) prostate cancer cells.

Authors:  Cindy Tran; Oliver Richmond; Latayia Aaron; Joann B Powell
Journal:  Biochem Pharmacol       Date:  2012-12-22       Impact factor: 5.858

6.  Chlorophyllin significantly reduces benzo[a]pyrene-DNA adduct formation and alters cytochrome P450 1A1 and 1B1 expression and EROD activity in normal human mammary epithelial cells.

Authors:  Channa Keshava; Rao L Divi; Tracey L Einem; Diana L Richardson; Sarah L Leonard; Nagalakshmi Keshava; Miriam C Poirier; Ainsley Weston
Journal:  Environ Mol Mutagen       Date:  2009-03       Impact factor: 3.216

Review 7.  Xenobiotic, bile acid, and cholesterol transporters: function and regulation.

Authors:  Curtis D Klaassen; Lauren M Aleksunes
Journal:  Pharmacol Rev       Date:  2010-01-26       Impact factor: 25.468

8.  The aryl hydrocarbon receptor is constitutively active in advanced prostate cancer cells.

Authors:  Oliver Richmond; Maryam Ghotbaddini; Cidney Allen; Alice Walker; Shokouh Zahir; Joann B Powell
Journal:  PLoS One       Date:  2014-04-22       Impact factor: 3.240

Review 9.  The Ah Receptor: Adaptive Metabolism, Ligand Diversity, and the Xenokine Model.

Authors:  Mele N Avilla; Kristen M C Malecki; Mark E Hahn; Rachel H Wilson; Christopher A Bradfield
Journal:  Chem Res Toxicol       Date:  2020-04-07       Impact factor: 3.739

  9 in total

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