PLoS ONE (Jan 2011)

Association between Prostinogen (KLK15) genetic variants and prostate cancer risk and aggressiveness in Australia and a meta-analysis of GWAS data.

  • Jyotsna Batra,
  • Felicity Lose,
  • Tracy O'Mara,
  • Louise Marquart,
  • Carson Stephens,
  • Kimberly Alexander,
  • Srilakshmi Srinivasan,
  • Rosalind A Eeles,
  • Douglas F Easton,
  • Ali Amin Al Olama,
  • Zsofia Kote-Jarai,
  • Michelle Guy,
  • Kenneth Muir,
  • Artitaya Lophatananon,
  • Aneela A Rahman,
  • David E Neal,
  • Freddie C Hamdy,
  • Jenny L Donovan,
  • Suzanne Chambers,
  • Robert A Gardiner,
  • Joanne Aitken,
  • John Yaxley,
  • Mary-Anne Kedda,
  • Judith A Clements,
  • Amanda B Spurdle

DOI
https://doi.org/10.1371/journal.pone.0026527
Journal volume & issue
Vol. 6, no. 11
p. e26527

Abstract

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BackgroundKallikrein 15 (KLK15)/Prostinogen is a plausible candidate for prostate cancer susceptibility. Elevated KLK15 expression has been reported in prostate cancer and it has been described as an unfavorable prognostic marker for the disease.ObjectivesWe performed a comprehensive analysis of association of variants in the KLK15 gene with prostate cancer risk and aggressiveness by genotyping tagSNPs, as well as putative functional SNPs identified by extensive bioinformatics analysis. METHODS AND DATA SOURCES: Twelve out of 22 SNPs, selected on the basis of linkage disequilibrium pattern, were analyzed in an Australian sample of 1,011 histologically verified prostate cancer cases and 1,405 ethnically matched controls. Replication was sought from two existing genome wide association studies (GWAS): the Cancer Genetic Markers of Susceptibility (CGEMS) project and a UK GWAS study.ResultsTwo KLK15 SNPs, rs2659053 and rs3745522, showed evidence of association (pConclusionsOur findings suggest a role for KLK15 genetic variation in the etiology of prostate cancer among men of European ancestry, although further studies in very large sample sets are necessary to confirm effect sizes.