Literature DB >> 18652561

Expression and activity of aryl hydrocarbon receptors in development and cancer.

Thomas A Gasiewicz1, Ellen C Henry, Loretta L Collins.   

Abstract

Although the aryl hydrocarbon receptor (AhR) has been known as the mediator of the toxicity of particular xenobiotics such as the dioxins, the normal role of this transcription factor in a number of biological processes is just beginning to be recognized. Knowledge of AhR-targeted genes and signaling pathways indicates involvement of AhR in fundamental cell-regulatory pathways. Noted defects in the morphology and functions of certain tissues in the absence of AhR point to critical roles for this protein in developmental processes. Together, the data suggest that the AhR has an important function in controlling the balance among processes involved in cell proliferation, death, and differentiation rather than being essential for them. On the other hand, deregulation of these processes is known to contribute to events such as tumor initiation, promotion, and progression that ultimately lead to malignant tumor formation. Epidemiological and experimental animal data, along with a more detailed understanding of how AhR is involved in regulating particular signaling pathways, provide substantial support for an association between abnormal AhR function and cancer. Here we describe the current understanding of how the AhR may function to regulate both normal and cancerous tissue growth and development.

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Year:  2008        PMID: 18652561     DOI: 10.1615/critreveukargeneexpr.v18.i4.10

Source DB:  PubMed          Journal:  Crit Rev Eukaryot Gene Expr        ISSN: 1045-4403            Impact factor:   1.807


  37 in total

1.  Activation of the aryl hydrocarbon receptor during pregnancy in the mouse alters mammary development through direct effects on stromal and epithelial tissues.

Authors:  Betina J Lew; Ravikumar Manickam; B Paige Lawrence
Journal:  Biol Reprod       Date:  2011-01-26       Impact factor: 4.285

Review 2.  The aryl hydrocarbon receptor: regulation of hematopoiesis and involvement in the progression of blood diseases.

Authors:  Fanny L Casado; Kameshwar P Singh; Thomas A Gasiewicz
Journal:  Blood Cells Mol Dis       Date:  2010-02-19       Impact factor: 3.039

3.  The aryl hydrocarbon receptor contributes to the proliferation of human medulloblastoma cells.

Authors:  Daniel P Dever; Lisa A Opanashuk
Journal:  Mol Pharmacol       Date:  2012-02-06       Impact factor: 4.436

4.  Aryl hydrocarbon receptor-null allele mice have hematopoietic stem/progenitor cells with abnormal characteristics and functions.

Authors:  Kameshwar P Singh; Russell W Garrett; Fanny L Casado; Thomas A Gasiewicz
Journal:  Stem Cells Dev       Date:  2010-11-09       Impact factor: 3.272

Review 5.  Indole and Tryptophan Metabolism: Endogenous and Dietary Routes to Ah Receptor Activation.

Authors:  Troy D Hubbard; Iain A Murray; Gary H Perdew
Journal:  Drug Metab Dispos       Date:  2015-06-03       Impact factor: 3.922

Review 6.  Xenobiotic metabolism, disposition, and regulation by receptors: from biochemical phenomenon to predictors of major toxicities.

Authors:  Curtis J Omiecinski; John P Vanden Heuvel; Gary H Perdew; Jeffrey M Peters
Journal:  Toxicol Sci       Date:  2010-11-08       Impact factor: 4.849

Review 7.  The aryl hydrocarbon receptor has a normal function in the regulation of hematopoietic and other stem/progenitor cell populations.

Authors:  Kameshwar P Singh; Fanny L Casado; Lisa A Opanashuk; Thomas A Gasiewicz
Journal:  Biochem Pharmacol       Date:  2008-10-15       Impact factor: 5.858

8.  Treatment of mice with the Ah receptor agonist and human carcinogen dioxin results in altered numbers and function of hematopoietic stem cells.

Authors:  Kameshwar P Singh; Amber Wyman; Fanny L Casado; Russell W Garrett; Thomas A Gasiewicz
Journal:  Carcinogenesis       Date:  2008-09-26       Impact factor: 4.944

9.  TCDD and a putative endogenous AhR ligand, ITE, elicit the same immediate changes in gene expression in mouse lung fibroblasts.

Authors:  Ellen C Henry; Stephen L Welle; Thomas A Gasiewicz
Journal:  Toxicol Sci       Date:  2009-11-19       Impact factor: 4.849

10.  TCDD exposure disrupts mammary epithelial cell differentiation and function.

Authors:  Loretta L Collins; Betina J Lew; B Paige Lawrence
Journal:  Reprod Toxicol       Date:  2009-03-13       Impact factor: 3.143

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