Assay of the c-erbB-2 oncogene encoded protein by ELISA and immunocytochemistry in human breast cancer

Ann Clin Biochem. 1994 Mar:31 ( Pt 2):171-3. doi: 10.1177/000456329403100210.

Abstract

The c-erbB-2 gene is amplified in a wide variety of different adenocarcinomas. Generally, gene amplification correlates with increased expression of the c-erbB-2 oncoprotein. Previous assays for the c-erbB-2 oncoprotein have been qualitative or semi-quantitative. In this investigation using human breast cancers, c-erbB-2 oncoprotein levels as measured by enzyme-linked immunosorbent assay (ELISA) correlated significantly with semi-quantitation by immunocytochemistry (r = 0.843, P < 0.0001, n = 97). The cut-off point for the ELISA which gave the strongest agreement with immunocytochemistry was 15 units/micrograms protein. It is concluded that detection of c-erbB-2 oncoprotein by ELISA is quantitative and objective.

Publication types

  • Comparative Study

MeSH terms

  • Biomarkers, Tumor / analysis*
  • Breast Neoplasms / chemistry*
  • Enzyme-Linked Immunosorbent Assay*
  • ErbB Receptors / analysis*
  • Humans
  • Immunohistochemistry*
  • Proto-Oncogene Proteins / analysis*
  • Receptor, ErbB-2

Substances

  • Biomarkers, Tumor
  • Proto-Oncogene Proteins
  • ErbB Receptors
  • Receptor, ErbB-2