HER-2/neu amplification predicts poor survival in node-positive breast cancer

Cancer Res. 1990 Jul 15;50(14):4332-7.

Abstract

HER-2/neu protooncogene amplification and protein expression were analyzed with slot blot and Western blot techniques, respectively, in more than 300 invasive primary breast tumors of all stages. Amplification (2- greater than 30 copies) was found in 17% of these tumors and high expression was seen in 19%. There was a striking coincidence between gene amplification and high expression. Tumors associated with many involved axillary lymph nodes or with Stage IV disease were more often HER-2/neu amplified or overexpressed. Furthermore, gene alteration was strongly correlated with the absence of steroid receptors and with larger tumor size. High expression without gene amplification was seen in a minor subset of tumors of less aggressive character. Neither amplification nor overexpression was correlated with disease outcome for patients with negative axillary lymph nodes. For node-positive patients, however, HER-2/neu amplification was a significant predictor of early relapse and death (median follow-up = 45 months), and a similar trend, although not significant, existed for high gene expression. Multivariate analyses indicated that HER-2/neu alterations were not independent predictors of patient outcome.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Biomarkers, Tumor / analysis*
  • Blotting, Western
  • Breast Neoplasms / analysis
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Female
  • Gene Amplification*
  • Gene Expression
  • Humans
  • Immune Sera
  • Lymphatic Metastasis
  • Menopause
  • Molecular Sequence Data
  • Peptides / chemical synthesis
  • Peptides / immunology
  • Prognosis
  • Protein-Tyrosine Kinases / genetics
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogenes*
  • Receptor, ErbB-2
  • Receptors, Estrogen / analysis
  • Receptors, Progesterone

Substances

  • Biomarkers, Tumor
  • Immune Sera
  • Peptides
  • Proto-Oncogene Proteins
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Protein-Tyrosine Kinases
  • Receptor, ErbB-2