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Role of Estrogen Receptor Signaling in Breast Cancer Metastasis

Metastatic breast cancer is a life-threatening stage of cancer and is the leading cause of death in advanced breast cancer patients. Estrogen signaling and the estrogen receptor (ER) are implicated in breast cancer progression, and the majority of the human breast cancers start out as estrogen depen...

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Detalles Bibliográficos
Autores principales: Saha Roy, Sudipa, Vadlamudi, Ratna K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262597/
https://www.ncbi.nlm.nih.gov/pubmed/22295247
http://dx.doi.org/10.1155/2012/654698
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author Saha Roy, Sudipa
Vadlamudi, Ratna K.
author_facet Saha Roy, Sudipa
Vadlamudi, Ratna K.
author_sort Saha Roy, Sudipa
collection PubMed
description Metastatic breast cancer is a life-threatening stage of cancer and is the leading cause of death in advanced breast cancer patients. Estrogen signaling and the estrogen receptor (ER) are implicated in breast cancer progression, and the majority of the human breast cancers start out as estrogen dependent. Accumulating evidence suggests that ER signaling is complex, involving coregulatory proteins and extranuclear actions. ER-coregualtory proteins are tightly regulated under normal conditions with miss expression primarily reported in cancer. Deregulation of ER coregualtors or ER extranuclear signaling has potential to promote metastasis in ER-positive breast cancer cells. This review summarizes the emerging role of ER signaling in promoting metastasis of breast cancer cells, discusses the molecular mechanisms by which ER signaling contributes to metastasis, and explores possible therapeutic targets to block ER-driven metastasis.
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spelling pubmed-32625972012-01-31 Role of Estrogen Receptor Signaling in Breast Cancer Metastasis Saha Roy, Sudipa Vadlamudi, Ratna K. Int J Breast Cancer Review Article Metastatic breast cancer is a life-threatening stage of cancer and is the leading cause of death in advanced breast cancer patients. Estrogen signaling and the estrogen receptor (ER) are implicated in breast cancer progression, and the majority of the human breast cancers start out as estrogen dependent. Accumulating evidence suggests that ER signaling is complex, involving coregulatory proteins and extranuclear actions. ER-coregualtory proteins are tightly regulated under normal conditions with miss expression primarily reported in cancer. Deregulation of ER coregualtors or ER extranuclear signaling has potential to promote metastasis in ER-positive breast cancer cells. This review summarizes the emerging role of ER signaling in promoting metastasis of breast cancer cells, discusses the molecular mechanisms by which ER signaling contributes to metastasis, and explores possible therapeutic targets to block ER-driven metastasis. Hindawi Publishing Corporation 2012 2011-12-19 /pmc/articles/PMC3262597/ /pubmed/22295247 http://dx.doi.org/10.1155/2012/654698 Text en Copyright © 2012 S. Saha Roy and R. K. Vadlamudi. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Saha Roy, Sudipa
Vadlamudi, Ratna K.
Role of Estrogen Receptor Signaling in Breast Cancer Metastasis
title Role of Estrogen Receptor Signaling in Breast Cancer Metastasis
title_full Role of Estrogen Receptor Signaling in Breast Cancer Metastasis
title_fullStr Role of Estrogen Receptor Signaling in Breast Cancer Metastasis
title_full_unstemmed Role of Estrogen Receptor Signaling in Breast Cancer Metastasis
title_short Role of Estrogen Receptor Signaling in Breast Cancer Metastasis
title_sort role of estrogen receptor signaling in breast cancer metastasis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262597/
https://www.ncbi.nlm.nih.gov/pubmed/22295247
http://dx.doi.org/10.1155/2012/654698
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