Germline BCL-2 sequence variants and inherited predisposition to prostate cancer

Prostate Cancer Prostatic Dis. 2006;9(3):284-92. doi: 10.1038/sj.pcan.4500884. Epub 2006 May 30.

Abstract

Apoptosis is an essential physiological process that regulates cellular proliferation. Here, we explored the effect of DNA sequence variation within the BCL-2 gene on prostate cancer susceptibility in three clinical populations, consisting of 428 African Americans, 214 Jamaicans and 218 European Americans. We observed a 70% reduced risk for prostate cancer among the European Americans who had possessed two copies of a promoter variant -938C/A. Additionally, common BCL-2 haplotypes appeared to influence prostate cancer risk; however, studies in larger data sets are needed to confirm our findings. Our data suggest that inherited BCL-2 variants may be associated with a decrease in prostate cancer susceptibility.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Black or African American / genetics
  • Carcinoma / genetics*
  • Case-Control Studies
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Genetic Variation*
  • Genotype
  • Germ-Line Mutation*
  • Haplotypes
  • Humans
  • Inheritance Patterns
  • Jamaica / ethnology
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Models, Biological
  • Open Reading Frames
  • Prostatic Neoplasms / genetics*
  • Proto-Oncogene Proteins c-bcl-2 / genetics*
  • Regulatory Elements, Transcriptional
  • White People / genetics

Substances

  • Proto-Oncogene Proteins c-bcl-2