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Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma
Limited studies have shown that some patients with pancreatic adenocarcinoma (PAC) may benefit from treatment with tamoxifen. PAC has been shown to be largely negative for estrogen receptor alpha (ER-alpha). The aim of this pilot study was to investigate ER-beta expression in human PAC. Sections of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340876/ https://www.ncbi.nlm.nih.gov/pubmed/30701026 http://dx.doi.org/10.18632/oncotarget.26503 |
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author | Younes, Mamoun Ly, Charles J. Singh, Kanchan Ertan, Atilla Younes, Pamela S. Bailey, Jennifer M. |
author_facet | Younes, Mamoun Ly, Charles J. Singh, Kanchan Ertan, Atilla Younes, Pamela S. Bailey, Jennifer M. |
author_sort | Younes, Mamoun |
collection | PubMed |
description | Limited studies have shown that some patients with pancreatic adenocarcinoma (PAC) may benefit from treatment with tamoxifen. PAC has been shown to be largely negative for estrogen receptor alpha (ER-alpha). The aim of this pilot study was to investigate ER-beta expression in human PAC. Sections of tissue microarray with 18 evaluable cases of human PAC were stained by immunohistochemistry (IHC) for ER-beta1, ER-beta2, ER-beta5, and Cyclin A. The levels of ER-beta isoform expression and the S-phase fraction (SPF) were determined using quantitative digital image analysis. Higher mean and median ER-beta2 levels correlated with male sex (p = 0.057 and p = 0.035, respectively), older age (p = 0.005 and p = 0.006, respectively), and lower pT stage (p = 0.008 and p = 0.009). Mean and median ER-beta5 levels correlated negatively with SPF (p = 0.021 and p = 0.047, respectively). Mean ER-beta1 expression did not correlate with any of the above mentioned clinicopathologic factors. The findings in this pilot study, although should be considered preliminary, suggest that some ER-beta isoforms may play a role in the biology of PAC. Additional larger studies are needed to confirm our findings, and to determine whether ER-beta may be considered for future targeted therapy. |
format | Online Article Text |
id | pubmed-6340876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-63408762019-01-30 Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma Younes, Mamoun Ly, Charles J. Singh, Kanchan Ertan, Atilla Younes, Pamela S. Bailey, Jennifer M. Oncotarget Research Paper Limited studies have shown that some patients with pancreatic adenocarcinoma (PAC) may benefit from treatment with tamoxifen. PAC has been shown to be largely negative for estrogen receptor alpha (ER-alpha). The aim of this pilot study was to investigate ER-beta expression in human PAC. Sections of tissue microarray with 18 evaluable cases of human PAC were stained by immunohistochemistry (IHC) for ER-beta1, ER-beta2, ER-beta5, and Cyclin A. The levels of ER-beta isoform expression and the S-phase fraction (SPF) were determined using quantitative digital image analysis. Higher mean and median ER-beta2 levels correlated with male sex (p = 0.057 and p = 0.035, respectively), older age (p = 0.005 and p = 0.006, respectively), and lower pT stage (p = 0.008 and p = 0.009). Mean and median ER-beta5 levels correlated negatively with SPF (p = 0.021 and p = 0.047, respectively). Mean ER-beta1 expression did not correlate with any of the above mentioned clinicopathologic factors. The findings in this pilot study, although should be considered preliminary, suggest that some ER-beta isoforms may play a role in the biology of PAC. Additional larger studies are needed to confirm our findings, and to determine whether ER-beta may be considered for future targeted therapy. Impact Journals LLC 2018-12-28 /pmc/articles/PMC6340876/ /pubmed/30701026 http://dx.doi.org/10.18632/oncotarget.26503 Text en Copyright: © 2018 Younes et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Younes, Mamoun Ly, Charles J. Singh, Kanchan Ertan, Atilla Younes, Pamela S. Bailey, Jennifer M. Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
title | Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
title_full | Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
title_fullStr | Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
title_full_unstemmed | Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
title_short | Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
title_sort | expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340876/ https://www.ncbi.nlm.nih.gov/pubmed/30701026 http://dx.doi.org/10.18632/oncotarget.26503 |
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