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Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
Authors:Gudmundsson Julius  Sulem Patrick  Steinthorsdottir Valgerdur  Bergthorsson Jon T  Thorleifsson Gudmar  Manolescu Andrei  Rafnar Thorunn  Gudbjartsson Daniel  Agnarsson Bjarni A  Baker Adam  Sigurdsson Asgeir  Benediktsdottir Kristrun R  Jakobsdottir Margret  Blondal Thorarinn  Stacey Simon N  Helgason Agnar  Gunnarsdottir Steinunn  Olafsdottir Adalheidur  Kristinsson Kari T  Birgisdottir Birgitta  Ghosh Shyamali  Thorlacius Steinunn  Magnusdottir Dana  Stefansdottir Gerdur  Kristjansson Kristleifur  Bagger Yu  Wilensky Robert L  Reilly Muredach P  Morris Andrew D  Kimber Charlotte H  Adeyemo Adebowale  Chen Yuanxiu
Affiliation:deCODE genetics, Sturlugata 8, 101 Reykjavik, Iceland. julius.gudmundsson@decode.is
Abstract:
We performed a genome-wide association scan to search for sequence variants conferring risk of prostate cancer using 1,501 Icelandic men with prostate cancer and 11,290 controls. Follow-up studies involving three additional case-control groups replicated an association of two variants on chromosome 17 with the disease. These two variants, 33 Mb apart, fall within a region previously implicated by family-based linkage studies on prostate cancer. The risks conferred by these variants are moderate individually (allele odds ratio of about 1.20), but because they are common, their joint population attributable risk is substantial. One of the variants is in TCF2 (HNF1beta), a gene known to be mutated in individuals with maturity-onset diabetes of the young type 5. Results from eight case-control groups, including one West African and one Chinese, demonstrate that this variant confers protection against type 2 diabetes.
Keywords:
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