Epithelial-cadherin gene is not mutated in ductal carcinomas of the breast

Jpn J Cancer Res. 1995 Nov;86(11):1054-9. doi: 10.1111/j.1349-7006.1995.tb03020.x.

Abstract

We investigated mutations of the epithelial (E)-cadherin gene and loss of heterozygosity (LOH) at flanking loci using three microsatellite markers on the long arm of chromosome 16 in 25 ductal carcinomas of the breast. Expression of E-cadherin was also investigated immunohistochemically. No mutations were detected in exons 6 through 9 of the E-cadherin gene. LOH was observed more frequently (42%) at D16S402 (16q-ter) than at D16S421 (16q22.3-q23.1) (17%), which is located near the E-cadherin gene. Expression of E-cadherin was observed at the cell borders in 92% (11/12) of the tumors examined. The absence of mutations in the E-cadherin gene and its conserved expression suggest that inactivation of E-cadherin does not contribute significantly to the invasion or metastatic potential of ductal carcinomas of the breast. Furthermore, the high frequency of LOH at 16q-ter suggests the existence of another tumor suppressor gene which may play a crucial role in the genesis of ductal carcinomas of the breast.

Publication types

  • Comparative Study

MeSH terms

  • Adenocarcinoma, Scirrhous / chemistry
  • Adenocarcinoma, Scirrhous / genetics
  • Adenocarcinoma, Scirrhous / pathology
  • Aneuploidy
  • Base Sequence
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Cadherins / analysis
  • Cadherins / genetics*
  • Carcinoma, Ductal, Breast / chemistry
  • Carcinoma, Ductal, Breast / genetics*
  • Carcinoma, Ductal, Breast / pathology
  • Carcinoma, Intraductal, Noninfiltrating / chemistry
  • Carcinoma, Intraductal, Noninfiltrating / genetics
  • Carcinoma, Intraductal, Noninfiltrating / pathology
  • Cell Adhesion
  • DNA, Neoplasm / genetics
  • DNA, Satellite / genetics
  • Humans
  • Molecular Sequence Data
  • Neoplasm Invasiveness
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Receptors, Estrogen / analysis

Substances

  • Cadherins
  • DNA, Neoplasm
  • DNA, Satellite
  • Neoplasm Proteins
  • Receptors, Estrogen