Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/45652
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dc.contributor.authorSeveri, G.en
dc.contributor.authorHayes, V.en
dc.contributor.authorTesoriero, A.en
dc.contributor.authorSouthey, M.en
dc.contributor.authorHoang, H.en
dc.contributor.authorPadilla, E.en
dc.contributor.authorMorris, H.en
dc.contributor.authorEnglish, D.en
dc.contributor.authorSutherland, R.en
dc.contributor.authorBoyle, P.en
dc.contributor.authorHopper, J.en
dc.contributor.authorGiles, G.en
dc.date.issued2008en
dc.identifier.citationBJU International, 2008; 101(4):492-496en
dc.identifier.issn1464-4096en
dc.identifier.issn1464-410Xen
dc.identifier.urihttp://hdl.handle.net/2440/45652-
dc.descriptionThe definitive version is available at www.blackwell-synergy.comen
dc.description.abstractOBJECTIVE: To use a large population-based case-control study to test the association between the common genetic variant rs743572 (−34 T to C), prostate cancer risk and circulating levels of several hormones. SUBJECTS AND METHODS: A previous meta-analysis concluded that reported associations between rs743572 in the promoter of CYP17A1 and prostate cancer risk might reflect publication bias, but a few recent studies reported associations with prostate cancer risk and data suggesting that rs743572 is functional. We genotyped 824 prostate cancer cases and 737 population-based controls, and applied unconditional logistic regression to estimate the association between rs743572 and prostate cancer risk. We also used linear regression of transformed testosterone, androstanediol glucuronide, dehydroepiandrosterone sulphate, androstenedione, sex hormone-binding globulin and oestradiol (circulating levels) measured for controls, to estimate the association between these levels and rs743572. The linear models were adjusted for age and laboratory batch. RESULTS: Men with different genotypes had similar circulating levels of all the hormones measured (all P < 0.05). In the case-control comparison using unconditional unadjusted logistic regression, the odds ratios (95% confidence interval) for prostate cancer were 1.07 (0.87–1.32) and 0.94 (0.71–1.25) for the dominant and recessive models, respectively, and for the co-dominant model, 1.10 (0.88–1.36) and 0.99 (0.73–1.35) for carriers of one or two copies of the C allele, respectively. There was no evidence of heterogeneity in the odds ratios by tumour stage (all P > 0.3) and grade (all P > 0.3). CONCLUSION: The results of the present study are consistent with the conclusions of the previous meta-analysis, and suggest that rs743572 has no role in the risk of prostate cancer for men of Caucasian origin.en
dc.description.statementofresponsibilityGianluca Severi, Vanessa M. Hayes, Andrea A. Tesoriero, Melissa C. Southey, Hoa N. Hoang, Emma J.D. Padilla, Howard A. Morris, Dallas R. English, Robert L. Sutherland, Peter Boyle, John L. Hopper and Graham G. Gilesen
dc.language.isoenen
dc.publisherBlackwell Publishing Ltden
dc.rightsCopyright © 2007 The Authorsen
dc.subjectHumans; Prostatic Neoplasms; Hormones; Steroid 17-alpha-Hydroxylase; Neoplasm Staging; Risk Factors; Case-Control Studies; Alleles; Aged; Middle Aged; Male; Promoter Regions, Geneticen
dc.titleThe rs743572 common variant in the promoter of CYP17A1 is not associated with prostate cancer risk or circulating hormonal levelsen
dc.typeJournal articleen
dc.identifier.doi10.1111/j.1464-410X.2007.07272.xen
pubs.publication-statusPublisheden
dc.identifier.orcidMorris, H. [0000-0002-2745-3750]en
Appears in Collections:Molecular and Biomedical Science publications

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