Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11

Lingyi Lu, Jielin Sun, Sarah D. Isaacs, Kathleen E. Wiley, Shelly Smith, Kristen Pruett, Yi Zhu, Zheng Zhang, Fredrik Wiklund, Henrik Grönberg, Patrick Walsh, Bao Li Chang, S. Lilly Zheng, William B Isaacs, Jianfeng Xu

Research output: Contribution to journalArticle

Abstract

Two single nucleotide polymorphisms (SNP; rs5945572 and rs5945619) at Xp11 were recently implicated in two genome-wide association studies of prostate cancer. Using a family-based association test for these two SNPs in 168 families with prostate cancer, we showed in this study that the risk alleles of the two reported SNPs were overtransmitted to the affected offspring (P = 0.009 for rs5945372 and P = 0.03 for rs5945619), which suggested that the observed association in case-control studies were not driven by potential population stratification. We also did a fine-mapping study in the f800 kb region at Xp11 between two independent case-control studies, including 1,527 cases and 482 controls from Johns Hopkins Hospital and 1,172 cases and 1,157 controls from the Prostate, Lung, Colon and Ovarian Cancer screening trial. The strongest association was found with SNPs in the haplotype block in which the two initial reported SNPs were located, although many SNPs in the ̃140 kb region were highly significant in the combined allelic tests (P = 10-5 to 10 -6). The second strongest association was observed with SNPs in the f286 kb region at another haplotype block (P = 10-4 to 10 -5),̃94 kb centromeric to the first region. The significance of SNPs in the second region decreased considerably after adjusting for SNPs at the first region, although P values remained at

Original languageEnglish (US)
Pages (from-to)2132-2136
Number of pages5
JournalCancer Epidemiology Biomarkers and Prevention
Volume18
Issue number7
DOIs
StatePublished - Jul 2009

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Single Nucleotide Polymorphism
Prostatic Neoplasms
Haplotypes
Case-Control Studies
Genome-Wide Association Study
Early Detection of Cancer
Ovarian Neoplasms
Colonic Neoplasms
Lung Neoplasms
Alleles
Population

ASJC Scopus subject areas

  • Epidemiology
  • Oncology

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Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11. / Lu, Lingyi; Sun, Jielin; Isaacs, Sarah D.; Wiley, Kathleen E.; Smith, Shelly; Pruett, Kristen; Zhu, Yi; Zhang, Zheng; Wiklund, Fredrik; Grönberg, Henrik; Walsh, Patrick; Chang, Bao Li; Zheng, S. Lilly; Isaacs, William B; Xu, Jianfeng.

In: Cancer Epidemiology Biomarkers and Prevention, Vol. 18, No. 7, 07.2009, p. 2132-2136.

Research output: Contribution to journalArticle

Lu, L, Sun, J, Isaacs, SD, Wiley, KE, Smith, S, Pruett, K, Zhu, Y, Zhang, Z, Wiklund, F, Grönberg, H, Walsh, P, Chang, BL, Zheng, SL, Isaacs, WB & Xu, J 2009, 'Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11', Cancer Epidemiology Biomarkers and Prevention, vol. 18, no. 7, pp. 2132-2136. https://doi.org/10.1158/1055-9965.EPI-08-1221
Lu, Lingyi ; Sun, Jielin ; Isaacs, Sarah D. ; Wiley, Kathleen E. ; Smith, Shelly ; Pruett, Kristen ; Zhu, Yi ; Zhang, Zheng ; Wiklund, Fredrik ; Grönberg, Henrik ; Walsh, Patrick ; Chang, Bao Li ; Zheng, S. Lilly ; Isaacs, William B ; Xu, Jianfeng. / Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11. In: Cancer Epidemiology Biomarkers and Prevention. 2009 ; Vol. 18, No. 7. pp. 2132-2136.
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