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The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?

In the nine years since the unexpected discovery of a second form of the estrogen receptor (ER), ERβ has been mentioned in about 2,800 literature citations. Such prolific research is testimony to interest in explaining its role in estrogen physiology as well as investigating its potential as a drug...

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Detalles Bibliográficos
Autor principal: Harris, Heather A.
Formato: Texto
Lenguaje:English
Publicado: The Nuclear Receptor Signaling Atlas 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513066/
https://www.ncbi.nlm.nih.gov/pubmed/16862218
http://dx.doi.org/10.1621/nrs.04012
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author Harris, Heather A.
author_facet Harris, Heather A.
author_sort Harris, Heather A.
collection PubMed
description In the nine years since the unexpected discovery of a second form of the estrogen receptor (ER), ERβ has been mentioned in about 2,800 literature citations. Such prolific research is testimony to interest in explaining its role in estrogen physiology as well as investigating its potential as a drug target. Our current understanding is that ERα, not ERβ is responsible for mediating the effects of estrogens in “classic” model systems such as the reproductive tract and skeleton. The role of ERβ is still being defined, but profiling of ERβ selective agonists in several animal models of human disease indicates these compounds may have utility as novel anti-inflammatory agents. The challenge for the future is to elucidate their mechanism of action and determine the clinical relevance of the impressive preclinical observations.
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spelling pubmed-15130662006-07-20 The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents? Harris, Heather A. Nucl Recept Signal Perspective In the nine years since the unexpected discovery of a second form of the estrogen receptor (ER), ERβ has been mentioned in about 2,800 literature citations. Such prolific research is testimony to interest in explaining its role in estrogen physiology as well as investigating its potential as a drug target. Our current understanding is that ERα, not ERβ is responsible for mediating the effects of estrogens in “classic” model systems such as the reproductive tract and skeleton. The role of ERβ is still being defined, but profiling of ERβ selective agonists in several animal models of human disease indicates these compounds may have utility as novel anti-inflammatory agents. The challenge for the future is to elucidate their mechanism of action and determine the clinical relevance of the impressive preclinical observations. The Nuclear Receptor Signaling Atlas 2006-07-07 /pmc/articles/PMC1513066/ /pubmed/16862218 http://dx.doi.org/10.1621/nrs.04012 Text en Copyright © 2006, Harris. This is an open-access article distributed under the terms of the Creative Commons Non-Commercial Attribution License, which permits unrestricted non-commercial use distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Perspective
Harris, Heather A.
The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
title The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
title_full The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
title_fullStr The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
title_full_unstemmed The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
title_short The unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
title_sort unexpected science of estrogen receptor-β selective agonists: a new class of anti-inflammatory agents?
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513066/
https://www.ncbi.nlm.nih.gov/pubmed/16862218
http://dx.doi.org/10.1621/nrs.04012
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