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Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers
Recent studies have identified the presence of estrogen receptor (ER)‐β in addition to ER‐α in human breast cancers, but the Clinicopathological characteristics of ER‐β‐positive tumors remain to be established. In this study, we have conducted an immunohistochemical analysis of ER‐α and ER‐β express...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926611/ https://www.ncbi.nlm.nih.gov/pubmed/11676856 http://dx.doi.org/10.1111/j.1349-7006.2001.tb01060.x |
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author | Miyoshi, Yasuo Taguchi, Tetsuya Gustafsson, Jan‐Åke Noguchi, Shinzaburo |
author_facet | Miyoshi, Yasuo Taguchi, Tetsuya Gustafsson, Jan‐Åke Noguchi, Shinzaburo |
author_sort | Miyoshi, Yasuo |
collection | PubMed |
description | Recent studies have identified the presence of estrogen receptor (ER)‐β in addition to ER‐α in human breast cancers, but the Clinicopathological characteristics of ER‐β‐positive tumors remain to be established. In this study, we have conducted an immunohistochemical analysis of ER‐α and ER‐β expression in human breast cancers. In addition, we investigated the correlation of ER‐α and ER‐β expression with progesterone receptor (PR) status, determined by enzyme immunoassay, and with various Clinicopathological factors. Of 79 tumors, 49 (62%) were positive for ER‐α and 24 (30%) were positive for ER‐β, and there was no significant association between ER‐α and ER‐β expression. ER‐α‐positive tumors were significantly more likely to be PR‐positive than were ER‐α‐negative tumors (P<0.0001), but there was no significant association between ER‐β expression and PR status. However, the PR values of ER‐α‐positive and ER‐β ‐positive tumors (65±17 fmol/mg protein, mean±SE) were marginally significantly lower than those of ER‐α‐positive and ER‐β ‐negative tumors (340±109) (P=0.08). ER‐β positivity was significantly associated with small tumor size (<2 cm) and high histological grade (P<0.05), and this association was also observed when only ER‐α‐positive tumors were considered. These results suggest that determination of ER‐β status might be clinically useful for further defining the characteristics of ER‐α‐positive tumors |
format | Online Article Text |
id | pubmed-5926611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59266112018-05-11 Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers Miyoshi, Yasuo Taguchi, Tetsuya Gustafsson, Jan‐Åke Noguchi, Shinzaburo Jpn J Cancer Res Article Recent studies have identified the presence of estrogen receptor (ER)‐β in addition to ER‐α in human breast cancers, but the Clinicopathological characteristics of ER‐β‐positive tumors remain to be established. In this study, we have conducted an immunohistochemical analysis of ER‐α and ER‐β expression in human breast cancers. In addition, we investigated the correlation of ER‐α and ER‐β expression with progesterone receptor (PR) status, determined by enzyme immunoassay, and with various Clinicopathological factors. Of 79 tumors, 49 (62%) were positive for ER‐α and 24 (30%) were positive for ER‐β, and there was no significant association between ER‐α and ER‐β expression. ER‐α‐positive tumors were significantly more likely to be PR‐positive than were ER‐α‐negative tumors (P<0.0001), but there was no significant association between ER‐β expression and PR status. However, the PR values of ER‐α‐positive and ER‐β ‐positive tumors (65±17 fmol/mg protein, mean±SE) were marginally significantly lower than those of ER‐α‐positive and ER‐β ‐negative tumors (340±109) (P=0.08). ER‐β positivity was significantly associated with small tumor size (<2 cm) and high histological grade (P<0.05), and this association was also observed when only ER‐α‐positive tumors were considered. These results suggest that determination of ER‐β status might be clinically useful for further defining the characteristics of ER‐α‐positive tumors Blackwell Publishing Ltd 2001-10 /pmc/articles/PMC5926611/ /pubmed/11676856 http://dx.doi.org/10.1111/j.1349-7006.2001.tb01060.x Text en |
spellingShingle | Article Miyoshi, Yasuo Taguchi, Tetsuya Gustafsson, Jan‐Åke Noguchi, Shinzaburo Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers |
title | Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers |
title_full | Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers |
title_fullStr | Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers |
title_full_unstemmed | Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers |
title_short | Clinicopathological Characteristics of Estrogen Receptor‐(3‐positive Human Breast Cancers |
title_sort | clinicopathological characteristics of estrogen receptor‐(3‐positive human breast cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926611/ https://www.ncbi.nlm.nih.gov/pubmed/11676856 http://dx.doi.org/10.1111/j.1349-7006.2001.tb01060.x |
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