Germline ATBF1 mutations and prostate cancer risk

Prostate. 2006 Jul 1;66(10):1082-5. doi: 10.1002/pros.20430.

Abstract

Background: ATBF1 has been recently identified as a candidate prostate tumor suppressor gene. In addition to more unique mutations, two somatic mutations (shortening of a polypyrimidine tract [Poly(T)n] and a deletion beginning at codon 3381 (3381del)) were each observed in multiple prostate cancer samples and both appear to have an impact on ATBF1 gene function and expression.

Methods: We assayed two recurrent sequence variants in germline DNA from prostate cancer cases and controls, and examined whether carriers of these variants are at increased risk for prostate cancer.

Results: We found Poly(T)n variants in both normal and matched tumor DNA samples from multiple patients, indicating a germline origin in each case. Genotyping germline DNA samples indicated that 3381del was significantly associated with prostate cancer risk among sporadic cases (P = 0.03), but not among men with hereditary disease.

Conclusions: Our study indicates that the germline 3381del allele may influence prostate cancer susceptibility.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Codon / genetics
  • DNA Mutational Analysis
  • DNA, Neoplasm / analysis
  • DNA, Neoplasm / blood
  • DNA, Neoplasm / genetics
  • Gene Deletion
  • Gene Frequency
  • Genes, Tumor Suppressor / physiology
  • Genetic Predisposition to Disease
  • Genotype
  • Germ-Line Mutation / genetics*
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / physiology*
  • Humans
  • Male
  • Middle Aged
  • Prostate / chemistry
  • Prostatic Neoplasms / chemistry
  • Prostatic Neoplasms / etiology
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / physiopathology*
  • Risk Factors

Substances

  • Codon
  • DNA, Neoplasm
  • Homeodomain Proteins
  • ZFHX3 protein, human