author_facet Barry, Kathryn Hughes
Moore, Lee E.
Sampson, Joshua
Yan, Liying
Meyer, Ann
Oler, Andrew J.
Chung, Charles C.
Wang, Zhaoming
Yeager, Meredith
Amundadottir, Laufey
Berndt, Sonja I.
Barry, Kathryn Hughes
Moore, Lee E.
Sampson, Joshua
Yan, Liying
Meyer, Ann
Oler, Andrew J.
Chung, Charles C.
Wang, Zhaoming
Yeager, Meredith
Amundadottir, Laufey
Berndt, Sonja I.
author Barry, Kathryn Hughes
Moore, Lee E.
Sampson, Joshua
Yan, Liying
Meyer, Ann
Oler, Andrew J.
Chung, Charles C.
Wang, Zhaoming
Yeager, Meredith
Amundadottir, Laufey
Berndt, Sonja I.
spellingShingle Barry, Kathryn Hughes
Moore, Lee E.
Sampson, Joshua
Yan, Liying
Meyer, Ann
Oler, Andrew J.
Chung, Charles C.
Wang, Zhaoming
Yeager, Meredith
Amundadottir, Laufey
Berndt, Sonja I.
Cancer Prevention Research
DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
Cancer Research
Oncology
author_sort barry, kathryn hughes
spelling Barry, Kathryn Hughes Moore, Lee E. Sampson, Joshua Yan, Liying Meyer, Ann Oler, Andrew J. Chung, Charles C. Wang, Zhaoming Yeager, Meredith Amundadottir, Laufey Berndt, Sonja I. 1940-6207 1940-6215 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1940-6207.capr-14-0132 <jats:title>Abstract</jats:title> <jats:p>Chromosome 8q24 has emerged as an important region for genetic susceptibility to various cancers, but little is known about the contribution of DNA methylation at 8q24. To evaluate variability in DNA methylation levels at 8q24 and the relationship with cancer susceptibility single nucleotide polymorphisms (SNPs) in this region, we quantified DNA methylation levels in peripheral blood at 145 CpG sites nearby 8q24 cancer susceptibility SNPs or MYC using pyrosequencing among 80 Caucasian men in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial. For the 60 CpG sites meeting quality control, which also demonstrated temporal stability over a 5-year period, we calculated pairwise Spearman correlations for DNA methylation levels at each CpG site with 42 8q24 cancer susceptibility SNPs. To account for multiple testing, we adjusted P values into q values reflecting the false discovery rate (FDR). In contrast to the MYC CpG sites, most sites nearby the SNPs demonstrated good reproducibility, high methylation levels, and moderate-high between-individual variation. We observed 10 statistically significant (FDR &amp;lt; 0.05) CpG site–SNP correlations. These included correlations between an intergenic CpG site at Chr8:128393157 and the prostate cancer SNP rs16902094 (ρ = −0.54; P = 9.7 × 10−7; q = 0.002), a PRNCR1 CpG site at Chr8:128167809 and the prostate cancer SNP rs1456315 (ρ = 0.52; P = 1.4 × 10−6; q = 0.002), and two POU5F1B CpG sites and several prostate/colorectal cancer SNPs (for Chr8:128498051 and rs6983267, ρ = 0.46; P = 2.0 × 10−5; q = 0.01). This is the first report of correlations between blood DNA methylation levels and cancer susceptibility SNPs at 8q24, suggesting that DNA methylation at this important susceptibility locus may contribute to cancer risk. Cancer Prev Res; 7(12); 1282–92. ©2014 AACR.</jats:p> DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci Cancer Prevention Research
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recordtype ai
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series Cancer Prevention Research
source_id 49
title DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_unstemmed DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_full DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_fullStr DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_full_unstemmed DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_short DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_sort dna methylation levels at chromosome 8q24 in peripheral blood are associated with 8q24 cancer susceptibility loci
topic Cancer Research
Oncology
url http://dx.doi.org/10.1158/1940-6207.capr-14-0132
publishDate 2014
physical 1282-1292
description <jats:title>Abstract</jats:title> <jats:p>Chromosome 8q24 has emerged as an important region for genetic susceptibility to various cancers, but little is known about the contribution of DNA methylation at 8q24. To evaluate variability in DNA methylation levels at 8q24 and the relationship with cancer susceptibility single nucleotide polymorphisms (SNPs) in this region, we quantified DNA methylation levels in peripheral blood at 145 CpG sites nearby 8q24 cancer susceptibility SNPs or MYC using pyrosequencing among 80 Caucasian men in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial. For the 60 CpG sites meeting quality control, which also demonstrated temporal stability over a 5-year period, we calculated pairwise Spearman correlations for DNA methylation levels at each CpG site with 42 8q24 cancer susceptibility SNPs. To account for multiple testing, we adjusted P values into q values reflecting the false discovery rate (FDR). In contrast to the MYC CpG sites, most sites nearby the SNPs demonstrated good reproducibility, high methylation levels, and moderate-high between-individual variation. We observed 10 statistically significant (FDR &amp;lt; 0.05) CpG site–SNP correlations. These included correlations between an intergenic CpG site at Chr8:128393157 and the prostate cancer SNP rs16902094 (ρ = −0.54; P = 9.7 × 10−7; q = 0.002), a PRNCR1 CpG site at Chr8:128167809 and the prostate cancer SNP rs1456315 (ρ = 0.52; P = 1.4 × 10−6; q = 0.002), and two POU5F1B CpG sites and several prostate/colorectal cancer SNPs (for Chr8:128498051 and rs6983267, ρ = 0.46; P = 2.0 × 10−5; q = 0.01). This is the first report of correlations between blood DNA methylation levels and cancer susceptibility SNPs at 8q24, suggesting that DNA methylation at this important susceptibility locus may contribute to cancer risk. Cancer Prev Res; 7(12); 1282–92. ©2014 AACR.</jats:p>
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author Barry, Kathryn Hughes, Moore, Lee E., Sampson, Joshua, Yan, Liying, Meyer, Ann, Oler, Andrew J., Chung, Charles C., Wang, Zhaoming, Yeager, Meredith, Amundadottir, Laufey, Berndt, Sonja I.
author_facet Barry, Kathryn Hughes, Moore, Lee E., Sampson, Joshua, Yan, Liying, Meyer, Ann, Oler, Andrew J., Chung, Charles C., Wang, Zhaoming, Yeager, Meredith, Amundadottir, Laufey, Berndt, Sonja I., Barry, Kathryn Hughes, Moore, Lee E., Sampson, Joshua, Yan, Liying, Meyer, Ann, Oler, Andrew J., Chung, Charles C., Wang, Zhaoming, Yeager, Meredith, Amundadottir, Laufey, Berndt, Sonja I.
author_sort barry, kathryn hughes
container_issue 12
container_start_page 1282
container_title Cancer Prevention Research
container_volume 7
description <jats:title>Abstract</jats:title> <jats:p>Chromosome 8q24 has emerged as an important region for genetic susceptibility to various cancers, but little is known about the contribution of DNA methylation at 8q24. To evaluate variability in DNA methylation levels at 8q24 and the relationship with cancer susceptibility single nucleotide polymorphisms (SNPs) in this region, we quantified DNA methylation levels in peripheral blood at 145 CpG sites nearby 8q24 cancer susceptibility SNPs or MYC using pyrosequencing among 80 Caucasian men in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial. For the 60 CpG sites meeting quality control, which also demonstrated temporal stability over a 5-year period, we calculated pairwise Spearman correlations for DNA methylation levels at each CpG site with 42 8q24 cancer susceptibility SNPs. To account for multiple testing, we adjusted P values into q values reflecting the false discovery rate (FDR). In contrast to the MYC CpG sites, most sites nearby the SNPs demonstrated good reproducibility, high methylation levels, and moderate-high between-individual variation. We observed 10 statistically significant (FDR &amp;lt; 0.05) CpG site–SNP correlations. These included correlations between an intergenic CpG site at Chr8:128393157 and the prostate cancer SNP rs16902094 (ρ = −0.54; P = 9.7 × 10−7; q = 0.002), a PRNCR1 CpG site at Chr8:128167809 and the prostate cancer SNP rs1456315 (ρ = 0.52; P = 1.4 × 10−6; q = 0.002), and two POU5F1B CpG sites and several prostate/colorectal cancer SNPs (for Chr8:128498051 and rs6983267, ρ = 0.46; P = 2.0 × 10−5; q = 0.01). This is the first report of correlations between blood DNA methylation levels and cancer susceptibility SNPs at 8q24, suggesting that DNA methylation at this important susceptibility locus may contribute to cancer risk. Cancer Prev Res; 7(12); 1282–92. ©2014 AACR.</jats:p>
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spelling Barry, Kathryn Hughes Moore, Lee E. Sampson, Joshua Yan, Liying Meyer, Ann Oler, Andrew J. Chung, Charles C. Wang, Zhaoming Yeager, Meredith Amundadottir, Laufey Berndt, Sonja I. 1940-6207 1940-6215 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1940-6207.capr-14-0132 <jats:title>Abstract</jats:title> <jats:p>Chromosome 8q24 has emerged as an important region for genetic susceptibility to various cancers, but little is known about the contribution of DNA methylation at 8q24. To evaluate variability in DNA methylation levels at 8q24 and the relationship with cancer susceptibility single nucleotide polymorphisms (SNPs) in this region, we quantified DNA methylation levels in peripheral blood at 145 CpG sites nearby 8q24 cancer susceptibility SNPs or MYC using pyrosequencing among 80 Caucasian men in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial. For the 60 CpG sites meeting quality control, which also demonstrated temporal stability over a 5-year period, we calculated pairwise Spearman correlations for DNA methylation levels at each CpG site with 42 8q24 cancer susceptibility SNPs. To account for multiple testing, we adjusted P values into q values reflecting the false discovery rate (FDR). In contrast to the MYC CpG sites, most sites nearby the SNPs demonstrated good reproducibility, high methylation levels, and moderate-high between-individual variation. We observed 10 statistically significant (FDR &amp;lt; 0.05) CpG site–SNP correlations. These included correlations between an intergenic CpG site at Chr8:128393157 and the prostate cancer SNP rs16902094 (ρ = −0.54; P = 9.7 × 10−7; q = 0.002), a PRNCR1 CpG site at Chr8:128167809 and the prostate cancer SNP rs1456315 (ρ = 0.52; P = 1.4 × 10−6; q = 0.002), and two POU5F1B CpG sites and several prostate/colorectal cancer SNPs (for Chr8:128498051 and rs6983267, ρ = 0.46; P = 2.0 × 10−5; q = 0.01). This is the first report of correlations between blood DNA methylation levels and cancer susceptibility SNPs at 8q24, suggesting that DNA methylation at this important susceptibility locus may contribute to cancer risk. Cancer Prev Res; 7(12); 1282–92. ©2014 AACR.</jats:p> DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci Cancer Prevention Research
spellingShingle Barry, Kathryn Hughes, Moore, Lee E., Sampson, Joshua, Yan, Liying, Meyer, Ann, Oler, Andrew J., Chung, Charles C., Wang, Zhaoming, Yeager, Meredith, Amundadottir, Laufey, Berndt, Sonja I., Cancer Prevention Research, DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci, Cancer Research, Oncology
title DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_full DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_fullStr DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_full_unstemmed DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_short DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
title_sort dna methylation levels at chromosome 8q24 in peripheral blood are associated with 8q24 cancer susceptibility loci
title_unstemmed DNA Methylation Levels at Chromosome 8q24 in Peripheral Blood Are Associated with 8q24 Cancer Susceptibility Loci
topic Cancer Research, Oncology
url http://dx.doi.org/10.1158/1940-6207.capr-14-0132