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Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis

BACKGROUND: The prognostic role of estrogen receptor beta (ERβ) in early-stage breast cancer is unclear. We performed a systematic review and meta-analysis to evaluate the prognostic value of ERβ in early-stage breast cancer patients. METHOD: We searched Medline, Embase, and the Web of Science for s...

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Autores principales: Tan, Weige, Li, Qian, Chen, Kai, Su, Fengxi, Song, Erwei, Gong, Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891126/
https://www.ncbi.nlm.nih.gov/pubmed/26863572
http://dx.doi.org/10.18632/oncotarget.7219
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author Tan, Weige
Li, Qian
Chen, Kai
Su, Fengxi
Song, Erwei
Gong, Chang
author_facet Tan, Weige
Li, Qian
Chen, Kai
Su, Fengxi
Song, Erwei
Gong, Chang
author_sort Tan, Weige
collection PubMed
description BACKGROUND: The prognostic role of estrogen receptor beta (ERβ) in early-stage breast cancer is unclear. We performed a systematic review and meta-analysis to evaluate the prognostic value of ERβ in early-stage breast cancer patients. METHOD: We searched Medline, Embase, and the Web of Science for studies published between 1990 and 2015 that assessed ERβ status in breast cancer patients. A total of 25 studies comprising 9919 patients fitting our inclusion and exclusion criteria were included. The hazard ratios of ERβ status were extracted for diseases free survival (DFS)/) and overall survival (OS). Random or fixed-effects models were used when appropriate, and between-study heterogeneity was assessed. RESULTS: In the 20 studies that assessed ERβ status using immunohistochemical (IHC) methods, we observed significantly improved DFS in patients positive for ERβ-1 (HR=0.56, 95%CI 0.40-0.78, P=0.0007) and ERβ-2 (HR=0.67, 95%CI 0.45-1.00, P=0.05). Improved OS was associated with a positive status for pan-ERβ (HR=0.60, 95%CI 0.45-0.80, P=0.0004) and ERβ-2 (HR=0.44, 95%CI 0.31-0.62, P<0.0001). In ERα-positive patients, ERβ positivity was not associated with DFS (HR=0.77, 95%CI 0.46-1.27, P=0.31) or OS (HR=0.64, 95%CI 0.37-1.11, P=0.11). In contrast, ERβ expression was significantly associated with increased DFS (HR=0.37, 95%CI 0.14-0.93, P=0.03) or OS (HR=0.44, 95%CI 0.30-0.65, P<0.0001) in ERα-negative patients. We did not observe an association between ERβ mRNA levels and DFS and OS. CONCLUSION: In this study, we showed that IHC ERβ status, rather than mRNA levels, is a prognostic factor that is associated with DFS and OS in breast cancer patients. The prognostic value of ERβ may be higher in ERα-negative patients than in ERα-positive patients.
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spelling pubmed-48911262016-06-23 Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis Tan, Weige Li, Qian Chen, Kai Su, Fengxi Song, Erwei Gong, Chang Oncotarget Research Paper BACKGROUND: The prognostic role of estrogen receptor beta (ERβ) in early-stage breast cancer is unclear. We performed a systematic review and meta-analysis to evaluate the prognostic value of ERβ in early-stage breast cancer patients. METHOD: We searched Medline, Embase, and the Web of Science for studies published between 1990 and 2015 that assessed ERβ status in breast cancer patients. A total of 25 studies comprising 9919 patients fitting our inclusion and exclusion criteria were included. The hazard ratios of ERβ status were extracted for diseases free survival (DFS)/) and overall survival (OS). Random or fixed-effects models were used when appropriate, and between-study heterogeneity was assessed. RESULTS: In the 20 studies that assessed ERβ status using immunohistochemical (IHC) methods, we observed significantly improved DFS in patients positive for ERβ-1 (HR=0.56, 95%CI 0.40-0.78, P=0.0007) and ERβ-2 (HR=0.67, 95%CI 0.45-1.00, P=0.05). Improved OS was associated with a positive status for pan-ERβ (HR=0.60, 95%CI 0.45-0.80, P=0.0004) and ERβ-2 (HR=0.44, 95%CI 0.31-0.62, P<0.0001). In ERα-positive patients, ERβ positivity was not associated with DFS (HR=0.77, 95%CI 0.46-1.27, P=0.31) or OS (HR=0.64, 95%CI 0.37-1.11, P=0.11). In contrast, ERβ expression was significantly associated with increased DFS (HR=0.37, 95%CI 0.14-0.93, P=0.03) or OS (HR=0.44, 95%CI 0.30-0.65, P<0.0001) in ERα-negative patients. We did not observe an association between ERβ mRNA levels and DFS and OS. CONCLUSION: In this study, we showed that IHC ERβ status, rather than mRNA levels, is a prognostic factor that is associated with DFS and OS in breast cancer patients. The prognostic value of ERβ may be higher in ERα-negative patients than in ERα-positive patients. Impact Journals LLC 2016-02-06 /pmc/articles/PMC4891126/ /pubmed/26863572 http://dx.doi.org/10.18632/oncotarget.7219 Text en Copyright: © 2016 Tan et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Tan, Weige
Li, Qian
Chen, Kai
Su, Fengxi
Song, Erwei
Gong, Chang
Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis
title Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis
title_full Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis
title_fullStr Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis
title_full_unstemmed Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis
title_short Estrogen receptor beta as a prognostic factor in breast cancer patients: A systematic review and meta-analysis
title_sort estrogen receptor beta as a prognostic factor in breast cancer patients: a systematic review and meta-analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891126/
https://www.ncbi.nlm.nih.gov/pubmed/26863572
http://dx.doi.org/10.18632/oncotarget.7219
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