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Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling

The diversity of membrane-initiated progesterone actions has made characterization and establishment of its biological importance a complicated endeavor. A new study by Zuo and colleagues shows that progesterone via endogenous membrane progesterone receptor-α acts as a negative regulator of prolifer...

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Detalles Bibliográficos
Autores principales: Sen, Aritro, Hammes, Stephen R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917021/
https://www.ncbi.nlm.nih.gov/pubmed/20561377
http://dx.doi.org/10.1186/bcr2580
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author Sen, Aritro
Hammes, Stephen R
author_facet Sen, Aritro
Hammes, Stephen R
author_sort Sen, Aritro
collection PubMed
description The diversity of membrane-initiated progesterone actions has made characterization and establishment of its biological importance a complicated endeavor. A new study by Zuo and colleagues shows that progesterone via endogenous membrane progesterone receptor-α acts as a negative regulator of proliferation and epithelial to mesenchymal transition in a breast cancer cell line. These progesterone-mediated actions appear to be regulated through epidermal growth factor receptor and phosphatidylinositol 3-kinase signaling localized in caveolae. Moreover, the study shows expression of membrane progesterone receptor-α in benign and malignant breast cancer tissues. These data bring forth novel concepts with regard to progesterone actions in the breast; however, further work is warranted to fully characterize the physiologic actions of extra-nuclear progesterone signaling in the breast.
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spelling pubmed-29170212010-12-16 Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling Sen, Aritro Hammes, Stephen R Breast Cancer Res Editorial The diversity of membrane-initiated progesterone actions has made characterization and establishment of its biological importance a complicated endeavor. A new study by Zuo and colleagues shows that progesterone via endogenous membrane progesterone receptor-α acts as a negative regulator of proliferation and epithelial to mesenchymal transition in a breast cancer cell line. These progesterone-mediated actions appear to be regulated through epidermal growth factor receptor and phosphatidylinositol 3-kinase signaling localized in caveolae. Moreover, the study shows expression of membrane progesterone receptor-α in benign and malignant breast cancer tissues. These data bring forth novel concepts with regard to progesterone actions in the breast; however, further work is warranted to fully characterize the physiologic actions of extra-nuclear progesterone signaling in the breast. BioMed Central 2010 2010-06-16 /pmc/articles/PMC2917021/ /pubmed/20561377 http://dx.doi.org/10.1186/bcr2580 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Editorial
Sen, Aritro
Hammes, Stephen R
Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
title Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
title_full Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
title_fullStr Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
title_full_unstemmed Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
title_short Just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
title_sort just when you thought it was safe to go into the membrane: the growing complexities of extra-nuclear progesterone signaling
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917021/
https://www.ncbi.nlm.nih.gov/pubmed/20561377
http://dx.doi.org/10.1186/bcr2580
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