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The orphan receptor ERRα interferes with steroid signaling

The estrogen receptor-related receptor α (ERRα) is an orphan member of the nuclear receptor superfamily that has been shown to interfere with the estrogen-signaling pathway. In this report, we demonstrate that ERRα also cross-talks with signaling driven by other steroid hormones. Treatment of human...

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Autores principales: Teyssier, Catherine, Bianco, Stéphanie, Lanvin, Olivia, Vanacker, Jean-Marc
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532727/
https://www.ncbi.nlm.nih.gov/pubmed/18697814
http://dx.doi.org/10.1093/nar/gkn520
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author Teyssier, Catherine
Bianco, Stéphanie
Lanvin, Olivia
Vanacker, Jean-Marc
author_facet Teyssier, Catherine
Bianco, Stéphanie
Lanvin, Olivia
Vanacker, Jean-Marc
author_sort Teyssier, Catherine
collection PubMed
description The estrogen receptor-related receptor α (ERRα) is an orphan member of the nuclear receptor superfamily that has been shown to interfere with the estrogen-signaling pathway. In this report, we demonstrate that ERRα also cross-talks with signaling driven by other steroid hormones. Treatment of human prostatic cells with a specific ERRα inverse agonist reduces the expression of several androgen-responsive genes, in a manner that does not involve perturbation of androgen receptor expression or activity. Furthermore, ERRα activates the expression of androgen response elements (ARE)-containing promoters, such as that of the prostate cancer marker PSA, in an ARE-dependent manner. In addition, promoters containing a steroid response element can be activated by all members of the ERR orphan receptor subfamily, and this, even in the presence of antisteroid compounds.
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spelling pubmed-25327272008-09-16 The orphan receptor ERRα interferes with steroid signaling Teyssier, Catherine Bianco, Stéphanie Lanvin, Olivia Vanacker, Jean-Marc Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The estrogen receptor-related receptor α (ERRα) is an orphan member of the nuclear receptor superfamily that has been shown to interfere with the estrogen-signaling pathway. In this report, we demonstrate that ERRα also cross-talks with signaling driven by other steroid hormones. Treatment of human prostatic cells with a specific ERRα inverse agonist reduces the expression of several androgen-responsive genes, in a manner that does not involve perturbation of androgen receptor expression or activity. Furthermore, ERRα activates the expression of androgen response elements (ARE)-containing promoters, such as that of the prostate cancer marker PSA, in an ARE-dependent manner. In addition, promoters containing a steroid response element can be activated by all members of the ERR orphan receptor subfamily, and this, even in the presence of antisteroid compounds. Oxford University Press 2008-09 2008-08-12 /pmc/articles/PMC2532727/ /pubmed/18697814 http://dx.doi.org/10.1093/nar/gkn520 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene regulation, Chromatin and Epigenetics
Teyssier, Catherine
Bianco, Stéphanie
Lanvin, Olivia
Vanacker, Jean-Marc
The orphan receptor ERRα interferes with steroid signaling
title The orphan receptor ERRα interferes with steroid signaling
title_full The orphan receptor ERRα interferes with steroid signaling
title_fullStr The orphan receptor ERRα interferes with steroid signaling
title_full_unstemmed The orphan receptor ERRα interferes with steroid signaling
title_short The orphan receptor ERRα interferes with steroid signaling
title_sort orphan receptor errα interferes with steroid signaling
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532727/
https://www.ncbi.nlm.nih.gov/pubmed/18697814
http://dx.doi.org/10.1093/nar/gkn520
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