Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.

A recent ovarian cancer genome-wide association study (GWAS) identified a locus on 9p22 associated with reduced ovarian cancer risk. The single nucleotide polymorphism (SNP) markers localize to the BNC2 gene, which has been associated with ovarian development.We analyzed the association of 9p22 SNPs...

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Main Authors: Nicolas Wentzensen, Amanda Black, Kevin Jacobs, Hannah P Yang, Christine D Berg, Neil Caporaso, Ulrike Peters, Lawrence Ragard, Saundra S Buys, Stephen Chanock, Patricia Hartge
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3131287?pdf=render
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author Nicolas Wentzensen
Amanda Black
Kevin Jacobs
Hannah P Yang
Christine D Berg
Neil Caporaso
Ulrike Peters
Lawrence Ragard
Saundra S Buys
Stephen Chanock
Patricia Hartge
author_facet Nicolas Wentzensen
Amanda Black
Kevin Jacobs
Hannah P Yang
Christine D Berg
Neil Caporaso
Ulrike Peters
Lawrence Ragard
Saundra S Buys
Stephen Chanock
Patricia Hartge
author_sort Nicolas Wentzensen
collection DOAJ
description A recent ovarian cancer genome-wide association study (GWAS) identified a locus on 9p22 associated with reduced ovarian cancer risk. The single nucleotide polymorphism (SNP) markers localize to the BNC2 gene, which has been associated with ovarian development.We analyzed the association of 9p22 SNPs with transvaginal ultrasound (TVU) screening results and CA-125 blood levels from participants without ovarian cancer in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO); 1,106 women with adequate ultrasound screening results and available genotyping information were included in the study.We observed a significantly increased risk of abnormal suspicious TVU results for seven SNPs on 9p22, with odds ratios between 1.68 (95% CI: 1.04-2.72) for rs4961501 and 2.10 (95% CI: 1.31-3.38) for rs12379183. Associations were restricted to abnormal suspicious findings at the first TVU screen. We did not observe an association between 9p22 SNPs and CA-125 levels.Our findings suggest that 9p22 SNPs, which were found to be associated with decreased risk of ovarian cancer in a recent GWAS, are associated with sonographically detectable ovarian abnormalities. Our results corroborate the relevance of the 9p22 locus for ovarian biology. Further studies are required to understand the complex relationship between screening abnormalities and ovarian carcinogenesis and to evaluate whether this locus can influence the risk stratification of ovarian cancer screening.
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spelling doaj.art-3047cc10296d46859a661109d98c04922022-12-22T02:24:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2173110.1371/journal.pone.0021731Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.Nicolas WentzensenAmanda BlackKevin JacobsHannah P YangChristine D BergNeil CaporasoUlrike PetersLawrence RagardSaundra S BuysStephen ChanockPatricia HartgeA recent ovarian cancer genome-wide association study (GWAS) identified a locus on 9p22 associated with reduced ovarian cancer risk. The single nucleotide polymorphism (SNP) markers localize to the BNC2 gene, which has been associated with ovarian development.We analyzed the association of 9p22 SNPs with transvaginal ultrasound (TVU) screening results and CA-125 blood levels from participants without ovarian cancer in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO); 1,106 women with adequate ultrasound screening results and available genotyping information were included in the study.We observed a significantly increased risk of abnormal suspicious TVU results for seven SNPs on 9p22, with odds ratios between 1.68 (95% CI: 1.04-2.72) for rs4961501 and 2.10 (95% CI: 1.31-3.38) for rs12379183. Associations were restricted to abnormal suspicious findings at the first TVU screen. We did not observe an association between 9p22 SNPs and CA-125 levels.Our findings suggest that 9p22 SNPs, which were found to be associated with decreased risk of ovarian cancer in a recent GWAS, are associated with sonographically detectable ovarian abnormalities. Our results corroborate the relevance of the 9p22 locus for ovarian biology. Further studies are required to understand the complex relationship between screening abnormalities and ovarian carcinogenesis and to evaluate whether this locus can influence the risk stratification of ovarian cancer screening.http://europepmc.org/articles/PMC3131287?pdf=render
spellingShingle Nicolas Wentzensen
Amanda Black
Kevin Jacobs
Hannah P Yang
Christine D Berg
Neil Caporaso
Ulrike Peters
Lawrence Ragard
Saundra S Buys
Stephen Chanock
Patricia Hartge
Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
PLoS ONE
title Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
title_full Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
title_fullStr Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
title_full_unstemmed Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
title_short Genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
title_sort genetic variation on 9p22 is associated with abnormal ovarian ultrasound results in the prostate lung colorectal and ovarian cancer screening trial
url http://europepmc.org/articles/PMC3131287?pdf=render
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