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Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression
BACKGROUND: Experimental studies have shown androgen receptor stimulation to facilitate formation of the TMPRSS2:ERG gene fusion in prostate cell lines. No study has tested whether higher pre-diagnostic circulating sex hormone levels in men increase risk of developing TMPRSS2:ERG-positive prostate c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984801/ https://www.ncbi.nlm.nih.gov/pubmed/26986253 http://dx.doi.org/10.1038/bjc.2016.61 |
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author | Graff, Rebecca E Meisner, Allison Ahearn, Thomas U Fiorentino, Michelangelo Loda, Massimo Giovannucci, Edward L Mucci, Lorelei A Pettersson, Andreas |
author_facet | Graff, Rebecca E Meisner, Allison Ahearn, Thomas U Fiorentino, Michelangelo Loda, Massimo Giovannucci, Edward L Mucci, Lorelei A Pettersson, Andreas |
author_sort | Graff, Rebecca E |
collection | PubMed |
description | BACKGROUND: Experimental studies have shown androgen receptor stimulation to facilitate formation of the TMPRSS2:ERG gene fusion in prostate cell lines. No study has tested whether higher pre-diagnostic circulating sex hormone levels in men increase risk of developing TMPRSS2:ERG-positive prostate cancer specifically. METHODS: We conducted a nested case–control study of 200 prostate cancer cases and 1057 controls from the Physicians' Health Study and Health Professionals Follow-up Study. We examined associations between pre-diagnostic circulating levels of total testosterone, free testosterone, DHT, androstanediol glucuronide, estradiol, and SHBG and risk of prostate cancer by TMPRSS2:ERG status. TMPRSS2:ERG was estimated by ERG immunohistochemistry. We used multivariable unconditional polytomous logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for risk of ERG-positive (n=94) and, separately, ERG-negative (n=106) disease. RESULTS: Free testosterone was significantly associated with the risk of ERG-positive prostate cancer (OR: 1.37, 95% CI: 1.05–1.77), but not ERG-negative prostate cancer (OR: 1.09, 95% CI: 0.86–1.38) (P(diff)=0.17). None of the remaining hormones evaluated showed clear differential associations with ERG-positive vs ERG-negative disease. CONCLUSIONS: These findings provide some suggestive evidence that higher pre-diagnostic free testosterone levels are associated with an increased risk of developing TMPRSS2:ERG-positive prostate cancer. |
format | Online Article Text |
id | pubmed-4984801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49848012017-04-12 Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression Graff, Rebecca E Meisner, Allison Ahearn, Thomas U Fiorentino, Michelangelo Loda, Massimo Giovannucci, Edward L Mucci, Lorelei A Pettersson, Andreas Br J Cancer Genetics and Genomics BACKGROUND: Experimental studies have shown androgen receptor stimulation to facilitate formation of the TMPRSS2:ERG gene fusion in prostate cell lines. No study has tested whether higher pre-diagnostic circulating sex hormone levels in men increase risk of developing TMPRSS2:ERG-positive prostate cancer specifically. METHODS: We conducted a nested case–control study of 200 prostate cancer cases and 1057 controls from the Physicians' Health Study and Health Professionals Follow-up Study. We examined associations between pre-diagnostic circulating levels of total testosterone, free testosterone, DHT, androstanediol glucuronide, estradiol, and SHBG and risk of prostate cancer by TMPRSS2:ERG status. TMPRSS2:ERG was estimated by ERG immunohistochemistry. We used multivariable unconditional polytomous logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for risk of ERG-positive (n=94) and, separately, ERG-negative (n=106) disease. RESULTS: Free testosterone was significantly associated with the risk of ERG-positive prostate cancer (OR: 1.37, 95% CI: 1.05–1.77), but not ERG-negative prostate cancer (OR: 1.09, 95% CI: 0.86–1.38) (P(diff)=0.17). None of the remaining hormones evaluated showed clear differential associations with ERG-positive vs ERG-negative disease. CONCLUSIONS: These findings provide some suggestive evidence that higher pre-diagnostic free testosterone levels are associated with an increased risk of developing TMPRSS2:ERG-positive prostate cancer. Nature Publishing Group 2016-04-12 2016-03-17 /pmc/articles/PMC4984801/ /pubmed/26986253 http://dx.doi.org/10.1038/bjc.2016.61 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Genetics and Genomics Graff, Rebecca E Meisner, Allison Ahearn, Thomas U Fiorentino, Michelangelo Loda, Massimo Giovannucci, Edward L Mucci, Lorelei A Pettersson, Andreas Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression |
title | Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression |
title_full | Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression |
title_fullStr | Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression |
title_full_unstemmed | Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression |
title_short | Pre-diagnostic circulating sex hormone levels and risk of prostate cancer by ERG tumour protein expression |
title_sort | pre-diagnostic circulating sex hormone levels and risk of prostate cancer by erg tumour protein expression |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984801/ https://www.ncbi.nlm.nih.gov/pubmed/26986253 http://dx.doi.org/10.1038/bjc.2016.61 |
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