Cargando…
Expression of oestrogen receptor β and prognosis of colorectal cancer
BACKGROUND: Previous studies suggest that sex steroids influence colorectal cancer (CRC) carcinogenesis. The oestrogen receptor β (ERβ) is the predominantly expressed ER in the colon and loss of ERβ in CRC has been associated with advanced cancer stages. METHODS: Information on vital status by the e...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425967/ https://www.ncbi.nlm.nih.gov/pubmed/22828608 http://dx.doi.org/10.1038/bjc.2012.323 |
_version_ | 1782241439052201984 |
---|---|
author | Rudolph, A Toth, C Hoffmeister, M Roth, W Herpel, E Jansen, L Marx, A Brenner, H Chang-Claude, J |
author_facet | Rudolph, A Toth, C Hoffmeister, M Roth, W Herpel, E Jansen, L Marx, A Brenner, H Chang-Claude, J |
author_sort | Rudolph, A |
collection | PubMed |
description | BACKGROUND: Previous studies suggest that sex steroids influence colorectal cancer (CRC) carcinogenesis. The oestrogen receptor β (ERβ) is the predominantly expressed ER in the colon and loss of ERβ in CRC has been associated with advanced cancer stages. METHODS: Information on vital status by the end of 2009 was obtained for 1262 CRC patients recruited between 2003 and 2007. The ERβ expression was immunohistochemically measured and associations of ERβ scores with overall survival (OS), disease-specific survival (DSS) and disease-free survival (DFS) were evaluated using Cox proportional hazard models adjusted for prognostic factors, such as tumour stage and second primary tumours. RESULTS: Of the 1101 tumour samples with successful measurement, 535 were ERβ negative (48.6%), 381 (34.6%) showed moderate and 185 (16.8%) showed high ERβ expression. Compared with high ERβ expression, lack of ERβ was associated with higher cancer stages as well as greater tumour extent. In multivariate analyses, ERβ negativity was associated with an increased hazard ratio for death (HR=1.61, 95% CI 1.09–2.40, P=0.02), death attributed to CRC (HR=1.54, 95% CI 0.99–2.39, P=0.06) as well as a poorer DFS (DFS HR=1.64, 95% CI 1.23–3.36, P=0.04). The associations were stronger in stage I-III patients (OS HR=2.20, 95% CI 1.28–4.06, P=0.007, DSS HR=2.38, 95% CI 1.20–5.39, P=0.02, respectively). CONCLUSIONS: Lack of ERβ expression is associated with advanced cancer stages and independently associated with poor survival. |
format | Online Article Text |
id | pubmed-3425967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34259672013-08-21 Expression of oestrogen receptor β and prognosis of colorectal cancer Rudolph, A Toth, C Hoffmeister, M Roth, W Herpel, E Jansen, L Marx, A Brenner, H Chang-Claude, J Br J Cancer Molecular Diagnostics BACKGROUND: Previous studies suggest that sex steroids influence colorectal cancer (CRC) carcinogenesis. The oestrogen receptor β (ERβ) is the predominantly expressed ER in the colon and loss of ERβ in CRC has been associated with advanced cancer stages. METHODS: Information on vital status by the end of 2009 was obtained for 1262 CRC patients recruited between 2003 and 2007. The ERβ expression was immunohistochemically measured and associations of ERβ scores with overall survival (OS), disease-specific survival (DSS) and disease-free survival (DFS) were evaluated using Cox proportional hazard models adjusted for prognostic factors, such as tumour stage and second primary tumours. RESULTS: Of the 1101 tumour samples with successful measurement, 535 were ERβ negative (48.6%), 381 (34.6%) showed moderate and 185 (16.8%) showed high ERβ expression. Compared with high ERβ expression, lack of ERβ was associated with higher cancer stages as well as greater tumour extent. In multivariate analyses, ERβ negativity was associated with an increased hazard ratio for death (HR=1.61, 95% CI 1.09–2.40, P=0.02), death attributed to CRC (HR=1.54, 95% CI 0.99–2.39, P=0.06) as well as a poorer DFS (DFS HR=1.64, 95% CI 1.23–3.36, P=0.04). The associations were stronger in stage I-III patients (OS HR=2.20, 95% CI 1.28–4.06, P=0.007, DSS HR=2.38, 95% CI 1.20–5.39, P=0.02, respectively). CONCLUSIONS: Lack of ERβ expression is associated with advanced cancer stages and independently associated with poor survival. Nature Publishing Group 2012-08-21 2012-07-24 /pmc/articles/PMC3425967/ /pubmed/22828608 http://dx.doi.org/10.1038/bjc.2012.323 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Molecular Diagnostics Rudolph, A Toth, C Hoffmeister, M Roth, W Herpel, E Jansen, L Marx, A Brenner, H Chang-Claude, J Expression of oestrogen receptor β and prognosis of colorectal cancer |
title | Expression of oestrogen receptor β and prognosis of colorectal cancer |
title_full | Expression of oestrogen receptor β and prognosis of colorectal cancer |
title_fullStr | Expression of oestrogen receptor β and prognosis of colorectal cancer |
title_full_unstemmed | Expression of oestrogen receptor β and prognosis of colorectal cancer |
title_short | Expression of oestrogen receptor β and prognosis of colorectal cancer |
title_sort | expression of oestrogen receptor β and prognosis of colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425967/ https://www.ncbi.nlm.nih.gov/pubmed/22828608 http://dx.doi.org/10.1038/bjc.2012.323 |
work_keys_str_mv | AT rudolpha expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT tothc expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT hoffmeisterm expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT rothw expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT herpele expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT jansenl expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT marxa expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT brennerh expressionofoestrogenreceptorbandprognosisofcolorectalcancer AT changclaudej expressionofoestrogenreceptorbandprognosisofcolorectalcancer |