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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
Thorarinn Blondal1,
Stacey, Simon N.
Helgason, Agnar
Gunnarsdottir, Steinunn
Olafsdottir, Adalheidur
Kristinsson, Kari T.
Birgisdottir, Birgitta
Source :
Nature Genetics. Aug2007, Vol. 39 Issue 8, p977-983. 7p. 5 Charts, 1 Graph.
Publication Year :
2007

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 (HNF1β), 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10614036
Volume :
39
Issue :
8
Database :
Academic Search Index
Journal :
Nature Genetics
Publication Type :
Academic Journal
Accession number :
25960565
Full Text :
https://doi.org/10.1038/ng2062