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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...

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Autores principales: Graff, Rebecca E, Meisner, Allison, Ahearn, Thomas U, Fiorentino, Michelangelo, Loda, Massimo, Giovannucci, Edward L, Mucci, Lorelei A, Pettersson, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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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.
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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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