Allelic imbalance within the E-cadherin gene is an infrequent event in prostate carcinogenesis

Genes Chromosomes Cancer. 2000 Jan;27(1):104-9. doi: 10.1002/(sici)1098-2264(200001)27:1<104::aid-gcc13>3.0.co;2-6.

Abstract

By exploiting two single nucleotide polymorphisms (SNPs) located within the E-cadherin gene, at 16q22, we have determined the frequency of allelic imbalance at this proposed tumor suppressor locus in a series of human prostatic carcinoma DNA samples. Whereas results with seven highly polymorphic microsatellite markers flanking the E-cadherin locus confirmed the existence of three separate loci on chromosome 16, at which allelic imbalance increased with increasing loss of tumor cell differentiation, no allelic imbalance within the E-cadherin gene was detected either by single-strand conformational polymorphism analysis or by direct sequencing. We conclude that the loss of E-cadherin function observed in prostate cancer is not a result of allelic deletion. Genes Chromosomes Cancer 27:104-109, 2000.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Cadherins / genetics*
  • Chromosomes, Human, Pair 16 / genetics
  • Genotype
  • Humans
  • Loss of Heterozygosity*
  • Male
  • Microsatellite Repeats / genetics
  • Polymorphism, Single Nucleotide
  • Polymorphism, Single-Stranded Conformational
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology
  • Sequence Deletion

Substances

  • Cadherins