Infrequent mutation of the H-cadherin gene on chromosome 16q24 in human breast cancers

Jpn J Cancer Res. 1997 Aug;88(8):701-4. doi: 10.1111/j.1349-7006.1997.tb00439.x.

Abstract

To investigate the molecular basis of altered expression of the H-cadherin gene, we used polymerase chain reaction-single strand conformation polymorphism and DNA sequencing to examine the H-cadherin gene in 48 primary breast cancers in which loss of the long arm of chromosome 16 had been detected. We identified no mutations other than somatic 5-bp deletion within the coding region in a single tumor. The very low frequency of mutation found in these experiments suggests that H-cadherin is usually not a primary target for carcinogenesis in human breast cancers, and that reduction of its expression is likely to be a consequence of some other genetic event(s).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / genetics*
  • Cadherins / genetics*
  • Chromosomes, Human, Pair 16 / genetics*
  • DNA Mutational Analysis
  • DNA, Neoplasm / genetics*
  • Female
  • Humans
  • Neoplasm Proteins / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Sequence Deletion*

Substances

  • Cadherins
  • DNA, Neoplasm
  • H-cadherin
  • Neoplasm Proteins