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Genome-wide association study identifies new prostate cancer susceptibility loci
Vise andre og tillknytning
2011 (engelsk)Inngår i: Human Molecular Genetics, ISSN 0964-6906, E-ISSN 1460-2083, Vol. 20, nr 19, s. 3867-3875Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Prostate cancer (PrCa) is the most common non-skin cancer diagnosed among males in developed countries and the second leading cause of cancer mortality, yet little is known regarding its etiology and factors that influence clinical outcome. Genome-wide association studies (GWAS) of PrCa have identified at least 30 distinct loci associated with small differences in risk. We conducted a GWAS in 2782 advanced PrCa cases (Gleason grade >= 8 or tumor stage C/D) and 4458 controls with 571 243 single nucleotide polymorphisms (SNPs). Based on in silico replication of 4679 SNPs (Stage 1, P < 0.02) in two published GWAS with 7358 PrCa cases and 6732 controls, we identified a new susceptibility locus associated with overall PrCa risk at 2q37.3 (rs2292884, P = 4.3 x 10(-8)). We also confirmed a locus suggested by an earlier GWAS at 12q13 (rs902774, P = 8.6 x 10(-9)). The estimated per-allele odds ratios for these loci (1.14 for rs2292884 and 1.17 for rs902774) did not differ between advanced and non-advanced PrCa (case-only test for heterogeneity P = 0.72 and P = 0.61, respectively). Further studies will be needed to assess whether these or other loci are differentially associated with PrCa subtypes.

sted, utgiver, år, opplag, sider
London: IRL Press , 2011. Vol. 20, nr 19, s. 3867-3875
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URN: urn:nbn:se:umu:diva-47641DOI: 10.1093/hmg/ddr295ISI: 000294810000014OAI: oai:DiVA.org:umu-47641DiVA, id: diva2:444762
Tilgjengelig fra: 2011-09-30 Laget: 2011-09-27 Sist oppdatert: 2018-06-08bibliografisk kontrollert

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