Immunohistochemical study of c-erbB-2 oncoprotein overexpression in human major salivary gland carcinoma: an indicator of aggressiveness

Laryngoscope. 1992 Aug;102(8):923-7. doi: 10.1288/00005537-199208000-00013.

Abstract

In order to analyze the correlation between immunohistochemical positivity for c-erbB-2 oncoprotein and prognosis in patients with malignant salivary gland tumors, 59 cases of malignant tumors of the major salivary glands, including 35 parotid gland, 20 submaxillary gland and 4 sublingual gland tumors, were studied immunohistochemically using a polyclonal antibody against c-erbB-2 oncoprotein. Positive staining was observed in 13 (22%) of the 59 cases. Interestingly, positive results were obtained only in adenocarcinoma (6/20) and carcinoma in pleomorphic adenoma (7/15), and not in any other histological types such as adenoid cystic carcinoma, mucoepidermoid tumor, and squamous cell carcinoma. There was no correlation between the degree of differentiation of adenocarcinoma and c-erbB-2 positivity. Since the carcinoma in pleomorphic adenoma positive for c-erbB-2 oncoprotein was adenocarcinoma, adenocarcinoma and adenocarcinoma in pleomorphic adenoma were placed together (n = 33), and the presence or absence of c-erbB-2 oncoprotein in this group was examined for correlation with patients' survival and other clinicopathological features, including clinical stage, tumor size, surgical margins, and lymph node status. The c-erbB-2-positive tumors tended to be more advanced and larger than negative tumors. Similarly, c-erbB-2-positive tumors were difficult to resect completely, were associated with lymph node metastasis more frequently, and showed lower disease-free survival than negative cases (P less than .05). We conclude that immunohistochemical positivity for c-erbB-2 is an indicator of aggressiveness in both adenocarcinoma and adenocarcinoma in pleomorphic adenoma of the major salivary glands.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemistry*
  • Adenocarcinoma / genetics
  • Adenocarcinoma / pathology
  • Adenoma, Pleomorphic / chemistry
  • Adenoma, Pleomorphic / genetics
  • Adenoma, Pleomorphic / pathology
  • Biomarkers, Tumor / analysis*
  • Biomarkers, Tumor / genetics
  • Carcinoma / chemistry*
  • Carcinoma / genetics
  • Carcinoma / pathology
  • Gene Amplification
  • Gene Expression*
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis
  • Neoplasm Staging
  • Neoplasms, Germ Cell and Embryonal / chemistry
  • Neoplasms, Germ Cell and Embryonal / genetics
  • Neoplasms, Germ Cell and Embryonal / pathology
  • Neoplasms, Multiple Primary / chemistry
  • Neoplasms, Multiple Primary / genetics
  • Neoplasms, Multiple Primary / pathology
  • Parotid Neoplasms / chemistry
  • Parotid Neoplasms / genetics
  • Parotid Neoplasms / pathology
  • Protein-Tyrosine Kinases / analysis*
  • Protein-Tyrosine Kinases / genetics
  • Proto-Oncogene Proteins / analysis*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogenes / genetics*
  • Receptor, ErbB-2
  • Salivary Gland Neoplasms / chemistry*
  • Salivary Gland Neoplasms / genetics
  • Salivary Gland Neoplasms / pathology
  • Sublingual Gland Neoplasms / chemistry
  • Sublingual Gland Neoplasms / genetics
  • Sublingual Gland Neoplasms / pathology
  • Submandibular Gland Neoplasms / chemistry
  • Submandibular Gland Neoplasms / genetics
  • Submandibular Gland Neoplasms / pathology
  • Survival Rate

Substances

  • Biomarkers, Tumor
  • Proto-Oncogene Proteins
  • Protein-Tyrosine Kinases
  • Receptor, ErbB-2