Nuclear and flow cytometric characteristics associated with overexpression of the c-erbB-2 oncoprotein in breast carcinoma

Breast Cancer Res Treat. 1991 Dec;20(1):3-10. doi: 10.1007/BF01833351.

Abstract

The overexpression of the c-erbB-2 oncoprotein is now thought by most authors to be associated with adverse prognosis in breast carcinoma. In this study, we investigate the relationship between overexpression of the c-erbB-2 oncoprotein and nuclear size by morphometry in a series of 150 human breast carcinomas, comprising 65 cases of ductal carcinoma in situ (DCIS) and 85 cases of invasive adenocarcinoma. The mean nuclear size for c-erbB-2 positive cases of DCIS was 54.8 micron 2 and invasive carcinoma was 52.1 micron 2 respectively, in contrast with 41.6 micron 2 and 42.5 micron 2 for c-erbB-2 negative cases of DCIS and invasive carcinoma respectively. Flow cytometric examination of DNA in a subset of 91 of these tumours showed no association between tumour cell aneuploidy and c-erbB-2 overexpression. S-phase fraction could be calculated on 20 cases of DCIS and 48 invasive carcinomas. There was a strong association between c-erbB-2 overexpression, S-phase fraction (p less than 0.001) and proliferative index (p less than 0.001) in 20 cases of DCIS. A weak association of S-phase fraction and c-erbB-2 overexpression was seen in 48 invasive carcinomas (p = 0.047). This study confirms the subjective impression that there is a relationship between large tumour cell nuclear size and an overexpression of the c-erbB-2 oncoprotein, and also shows an association with increased tumour cell proliferation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemistry*
  • Adenocarcinoma / pathology
  • Aneuploidy
  • Biomarkers, Tumor / analysis*
  • Breast Neoplasms / chemistry*
  • Breast Neoplasms / pathology
  • Carcinoma, Intraductal, Noninfiltrating / chemistry*
  • Carcinoma, Intraductal, Noninfiltrating / pathology
  • Cell Division
  • Cell Nucleus / ultrastructure
  • DNA, Neoplasm / analysis
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Neoplasm Proteins / analysis*
  • Proto-Oncogene Proteins / analysis*
  • Receptor, ErbB-2
  • S Phase

Substances

  • Biomarkers, Tumor
  • DNA, Neoplasm
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Receptor, ErbB-2