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Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival
BACKGROUND: Altered androgen hormone homeostasis and androgen receptor (AR) activity have been implicated in ovarian carcinogenesis but the relationship between AR expression in ovarian cancer and clinical outcome remains unclear. METHODS: In this study, the prognostic impact of AR expression was in...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902477/ https://www.ncbi.nlm.nih.gov/pubmed/20565760 http://dx.doi.org/10.1186/1757-2215-3-14 |
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author | Nodin, Björn Zendehrokh, Nooreldin Brändstedt, Jenny Nilsson, Elise Manjer, Jonas Brennan, Donal J Jirström, Karin |
author_facet | Nodin, Björn Zendehrokh, Nooreldin Brändstedt, Jenny Nilsson, Elise Manjer, Jonas Brennan, Donal J Jirström, Karin |
author_sort | Nodin, Björn |
collection | PubMed |
description | BACKGROUND: Altered androgen hormone homeostasis and androgen receptor (AR) activity have been implicated in ovarian carcinogenesis but the relationship between AR expression in ovarian cancer and clinical outcome remains unclear. METHODS: In this study, the prognostic impact of AR expression was investigated using immunohistochemistry in tissue microarrays from 154 incident cases of epithelial ovarian cancer (EOC) in the prospective, population-based cohorts Malmö Diet and Cancer Study and Malmö Preventive Project. A subset of corresponding fallopian tubes (n = 36) with no histopathological evidence of disease was also analysed. RESULTS: While abundantly expressed in the majority of fallopian tubes with more than 75% positive nuclei in 16/36 (44%) cases, AR was absent in 108/154 (70%) of EOC cases. AR expression was not related to prognosis in the entire cohort, but in the serous subtype (n = 90), AR positivity (> 10% positive nuclei) was associated with a prolonged disease specific survival in univariate (HR= 0.49; 95% CI 0.25-0.96; p= 0.038) and multivariate (HR= 0.46; 95% CI 0.22-0.97; p= 0.042) analysis, adjusted for age, grade and clinical stage. CONCLUSIONS: AR expression is considerably reduced in EOC as compared to fallopian tubes, and in EOC of the serous subtype, high AR expression is a favourable prognostic factor. These results indicate that assessment of AR expression might be of value for treatment stratification of EOC patients with serous ovarian carcinoma. |
format | Text |
id | pubmed-2902477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29024772010-07-13 Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival Nodin, Björn Zendehrokh, Nooreldin Brändstedt, Jenny Nilsson, Elise Manjer, Jonas Brennan, Donal J Jirström, Karin J Ovarian Res Research BACKGROUND: Altered androgen hormone homeostasis and androgen receptor (AR) activity have been implicated in ovarian carcinogenesis but the relationship between AR expression in ovarian cancer and clinical outcome remains unclear. METHODS: In this study, the prognostic impact of AR expression was investigated using immunohistochemistry in tissue microarrays from 154 incident cases of epithelial ovarian cancer (EOC) in the prospective, population-based cohorts Malmö Diet and Cancer Study and Malmö Preventive Project. A subset of corresponding fallopian tubes (n = 36) with no histopathological evidence of disease was also analysed. RESULTS: While abundantly expressed in the majority of fallopian tubes with more than 75% positive nuclei in 16/36 (44%) cases, AR was absent in 108/154 (70%) of EOC cases. AR expression was not related to prognosis in the entire cohort, but in the serous subtype (n = 90), AR positivity (> 10% positive nuclei) was associated with a prolonged disease specific survival in univariate (HR= 0.49; 95% CI 0.25-0.96; p= 0.038) and multivariate (HR= 0.46; 95% CI 0.22-0.97; p= 0.042) analysis, adjusted for age, grade and clinical stage. CONCLUSIONS: AR expression is considerably reduced in EOC as compared to fallopian tubes, and in EOC of the serous subtype, high AR expression is a favourable prognostic factor. These results indicate that assessment of AR expression might be of value for treatment stratification of EOC patients with serous ovarian carcinoma. BioMed Central 2010-06-17 /pmc/articles/PMC2902477/ /pubmed/20565760 http://dx.doi.org/10.1186/1757-2215-3-14 Text en Copyright ©2010 Nodin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Nodin, Björn Zendehrokh, Nooreldin Brändstedt, Jenny Nilsson, Elise Manjer, Jonas Brennan, Donal J Jirström, Karin Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
title | Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
title_full | Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
title_fullStr | Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
title_full_unstemmed | Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
title_short | Increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
title_sort | increased androgen receptor expression in serous carcinoma of the ovary is associated with an improved survival |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902477/ https://www.ncbi.nlm.nih.gov/pubmed/20565760 http://dx.doi.org/10.1186/1757-2215-3-14 |
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