Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

Charles C. Chung, Julia Ciampa, Meredith Yeager, Kevin B. Jacobs, Sonja I. Berndt, Richard B. Hayes, Jesus Gonzalez-Bosquet, Peter Kraft, Sholom Wacholder, Nick Orr, Kai Yu, Amy Hutchinson, Joseph Boland, Quan Chen, Heather Spencer Feigelson, Michael J. Thun, W. Ryan Diver, Demetrius Albanes, Jarmo Virtamo, Stephanie WeinsteinFredrick R. Schumacher, Geraldine Cancel-Tassin, Olivier Cussenot, Antoine Valeri, Gerald L. Andriole, E. David Crawford, Christopher A. Haiman, Brian E. Henderson, Laurence Kolonel, Loic Le Marchand, Afshan Siddiq, Elio Riboli, Tim J. Key, Rudolf Kaaks, William B. Isaacs, Sarah D. Isaacs, Henrik Grönberg, Fredrik Wiklund, Jianfeng Xu, Lars J. Vatten, Kristian Hveem, Inger Njolstad, Daniela S. Gerhard, Margaret Tucker, Robert N. Hoover, Joseph F. Fraumeni, David J. Hunter, Gilles Thomas, Nilanjan Chatterjee, Stephen J. Chanock

Research output: Contribution to journalArticlepeer-review

38 Scopus citations


Genome-wide association studies have identified prostate cancer susceptibility alleles on chromosome 11q13. As part of the Cancer Genetic Markers of Susceptibility (CGEMS) Initiative, the region flanking the most significant marker, rs10896449, was fine mapped in 10 272 cases and 9123 controls of European origin (10 studies) using 120 common single nucleotide polymorphisms (SNPs) selected by a two-staged tagging strategy using HapMap SNPs. Single-locus analysis identified 18 SNPs below genome-wide significance (P < 10-8) with rs10896449 the most significant (P = 7.94 × 10-19). Multi-locus models that included significant SNPs sequentially identified a second association at rs12793759 [odds ratio (OR) = 1.14, P = 4.76 × 10-5, adjusted P = 0.004] that is independent of rs10896449 and remained significant after adjustment for multiple testing within the region. rs10896438, a proxy of previously reported rs12418451 (r2= 0.96), independent of both rs10896449 and rs12793759 was detected (OR = 1.07, P = 5.92 × 10-3, adjusted P = 0.054). Our observation of a recombination hotspot that separates rs10896438 from rs10896449 and rs12793759, and low linkage disequilibrium (rs10896449-rs12793759, r2= 0.17; r2=10896449-rs10896438, r2= 0.10; rs12793759- rs10896438, r2= 0.12) corroborate our finding of three independent signals. By analysis of tagged SNPs across ~123 kb using next generation sequencing of 63 controls of European origin, 1000 Genome and HapMap data, we observed multiple surrogates for the three independent signals marked by rs10896449 (n = 31), rs10896438 (n = 24) and rs12793759 (n = 8). Our results indicate that a complex architec- ture underlying the common variants contributing to prostate cancer risk at 11q13. We estimate that at least 63 common variants should be considered in future studies designed to investigate the biological basis of the multiple association signals.

Original languageEnglish
Article numberddr189
Pages (from-to)2869-2878
Number of pages10
JournalHuman molecular genetics
Issue number14
StatePublished - Jul 2011


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