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...
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Veröffentlicht in: | British journal of cancer 2016-04, Vol.114 (8), p.939-944 |
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Sprache: | eng |
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Zusammenfassung: | 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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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/bjc.2016.61 |