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Tamoxifen Action in ER-Negative Breast Cancer

Breast cancer is a highly heterogeneous disease. Tamoxifen is a selective estrogen receptor (ER) modulator and is mainly indicated for the treatment of breast cancer in postmenopausal women and postsurgery neoadjuvant therapy in ER-positive breast cancers. Interestingly, 5–10% of the ER-negative bre...

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Detalles Bibliográficos
Autores principales: Manna, Subrata, Holz, Marina K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792287/
https://www.ncbi.nlm.nih.gov/pubmed/26989346
http://dx.doi.org/10.4137/STI.S29901
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author Manna, Subrata
Holz, Marina K.
author_facet Manna, Subrata
Holz, Marina K.
author_sort Manna, Subrata
collection PubMed
description Breast cancer is a highly heterogeneous disease. Tamoxifen is a selective estrogen receptor (ER) modulator and is mainly indicated for the treatment of breast cancer in postmenopausal women and postsurgery neoadjuvant therapy in ER-positive breast cancers. Interestingly, 5–10% of the ER-negative breast cancers have also shown sensitivity to tamoxifen treatment. The involvement of molecular markers and/or signaling pathways independent of ER signaling has been implicated in tamoxifen sensitivity in the ER-negative subgroup. Studies reveal that variation in the expression of estrogen-related receptor alpha, ER subtype beta, tumor microenvironment, and epigenetics affects tamoxifen sensitivity. This review discusses the background of the research on the action of tamoxifen that may inspire future studies to explore effective therapeutic strategies for the treatment of ER-negative and triple-negative breast cancers, the latter being an aggressive disease with worse clinical outcome.
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spelling pubmed-47922872016-03-15 Tamoxifen Action in ER-Negative Breast Cancer Manna, Subrata Holz, Marina K. Sign Transduct Insights Article Breast cancer is a highly heterogeneous disease. Tamoxifen is a selective estrogen receptor (ER) modulator and is mainly indicated for the treatment of breast cancer in postmenopausal women and postsurgery neoadjuvant therapy in ER-positive breast cancers. Interestingly, 5–10% of the ER-negative breast cancers have also shown sensitivity to tamoxifen treatment. The involvement of molecular markers and/or signaling pathways independent of ER signaling has been implicated in tamoxifen sensitivity in the ER-negative subgroup. Studies reveal that variation in the expression of estrogen-related receptor alpha, ER subtype beta, tumor microenvironment, and epigenetics affects tamoxifen sensitivity. This review discusses the background of the research on the action of tamoxifen that may inspire future studies to explore effective therapeutic strategies for the treatment of ER-negative and triple-negative breast cancers, the latter being an aggressive disease with worse clinical outcome. 2016-02-10 /pmc/articles/PMC4792287/ /pubmed/26989346 http://dx.doi.org/10.4137/STI.S29901 Text en http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Article
Manna, Subrata
Holz, Marina K.
Tamoxifen Action in ER-Negative Breast Cancer
title Tamoxifen Action in ER-Negative Breast Cancer
title_full Tamoxifen Action in ER-Negative Breast Cancer
title_fullStr Tamoxifen Action in ER-Negative Breast Cancer
title_full_unstemmed Tamoxifen Action in ER-Negative Breast Cancer
title_short Tamoxifen Action in ER-Negative Breast Cancer
title_sort tamoxifen action in er-negative breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792287/
https://www.ncbi.nlm.nih.gov/pubmed/26989346
http://dx.doi.org/10.4137/STI.S29901
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