Genetic factors influencing prostate cancer risk in Norwegian men.

Published

Journal Article

Norway has one of the highest rates of death due to prostate cancer (PCa) in the world. To assess the contribution of both common and rare single nucleotide variants (SNPs) to the prostate cancer burden in Norway, we assessed the frequency of the established prostate cancer susceptibility allele, HOXB13 G84E, as well as a series of validated, common PCa risk SNPs in a Norwegian PCa population of 779 patients. The G84E allele was observed in 2.3% of patients compared to 0.7% of control individuals, OR = 3.8, P = 1 × 10-4. While there was a trend toward an earlier age at diagnosis, overall the clinicopathologic features of PCa were not significantly different in G84E carriers and non-carriers. Evaluation of 32 established common risk alleles revealed significant associations of risk alleles at 13 loci, including SNPs at 8q24, and near TET2, SLC22A3, NKX3-1, CASC8, MYC, DAP2IP, MSMB, HNF1B, PPP1R14A, and KLK2/3. When the data for each SNP are combined into a genetic risk score (GRS), Norwegian men within the top decile of GRS have over 5-fold greater risk to be diagnosed with PCa than men with GRS in the lowest decile. These results indicate that risk alleles of HOXB13 and common variant SNPs are important components of inherited PCa risk in the Norwegian population, although these factors appear to contribute little to the malignancy's aggressiveness.

Full Text

Duke Authors

Cited Authors

  • Chen, H; Ewing, CM; Zheng, S; Grindedaal, EM; Cooney, KA; Wiley, K; Djurovic, S; Andreassen, OA; Axcrona, K; Mills, IG; Xu, J; Maehle, L; Fosså, SD; Isaacs, WB

Published Date

  • February 2018

Published In

Volume / Issue

  • 78 / 3

Start / End Page

  • 186 - 192

PubMed ID

  • 29181843

Pubmed Central ID

  • 29181843

Electronic International Standard Serial Number (EISSN)

  • 1097-0045

Digital Object Identifier (DOI)

  • 10.1002/pros.23453

Language

  • eng

Conference Location

  • United States