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Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
Authors:Gudmundsson Julius  Sulem Patrick  Manolescu Andrei  Amundadottir Laufey T  Gudbjartsson Daniel  Helgason Agnar  Rafnar Thorunn  Bergthorsson Jon T  Agnarsson Bjarni A  Baker Adam  Sigurdsson Asgeir  Benediktsdottir Kristrun R  Jakobsdottir Margret  Xu Jianfeng  Blondal Thorarinn  Kostic Jelena  Sun Jielin  Ghosh Shyamali  Stacey Simon N  Mouy Magali  Saemundsdottir Jona  Backman Valgerdur M  Kristjansson Kristleifur  Tres Alejandro  Partin Alan W  Albers-Akkers Marjo T  Godino-Ivan Marcos Javier  Walsh Patrick C  Swinkels Dorine W  Navarrete Sebastian  Isaacs Sarah D  Aben Katja K  Graif Theresa  Cashy John
Institution:deCODE genetics, Sturlugata 8, 101 Reykjavik, Iceland.
Abstract:Prostate cancer is the most prevalent noncutaneous cancer in males in developed regions, with African American men having among the highest worldwide incidence and mortality rates. Here we report a second genetic variant in the 8q24 region that, in conjunction with another variant we recently discovered, accounts for about 11%-13% of prostate cancer cases in individuals of European descent and 31% of cases in African Americans. We made the current discovery through a genome-wide association scan of 1,453 affected Icelandic individuals and 3,064 controls using the Illumina HumanHap300 BeadChip followed by four replication studies. A key step in the discovery was the construction of a 14-SNP haplotype that efficiently tags a relatively uncommon (2%-4%) susceptibility variant in individuals of European descent that happens to be very common (approximately 42%) in African Americans. The newly identified variant shows a stronger association with affected individuals who have an earlier age at diagnosis.
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