Detection of c-erbB-2 and FGF-3 (INT-2) gene amplification in epithelial ovarian cancer

Int J Oncol. 2000 Jul;17(1):103-6. doi: 10.3892/ijo.17.1.103.

Abstract

We examined gene amplifications of the c-erbB-2 and FGF-3 gene in 48 epithelial ovarian cancers by differential PCR and addressed their association with clinico-pathological features including clinical outcome. Overall, 25.0 and 20.8% of ovarian cancers displayed amplified c-erbB-2 or FGF-3 gene, respectively. Amplification of the c-erbB-2 gene was significantly associated with particular histological cell types, higher histological grade, and low levels of serous CA125. However, there was no correlation between c-erbB-2 gene amplification and patient outcome. No correlation was observed between FGF-3 gene amplification and any clinico-pathological features including overall survival. These findings suggested that c-erbB-2 or FGF-3 gene amplification might be one of the oncogenic events implicated in the development of ovarian cancers, yet is not a useful prognostic marker.

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / genetics
  • CA-125 Antigen / blood
  • Carcinoma / genetics*
  • Carcinoma / mortality
  • Carcinoma / pathology
  • Carcinoma / surgery
  • Female
  • Fibroblast Growth Factor 3
  • Fibroblast Growth Factors / analysis
  • Fibroblast Growth Factors / genetics*
  • Follow-Up Studies
  • Gene Amplification*
  • Genes, erbB-2*
  • Humans
  • Middle Aged
  • Neoplasm Staging
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / mortality
  • Ovarian Neoplasms / pathology
  • Ovarian Neoplasms / surgery
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / genetics*
  • Receptor, ErbB-2 / analysis
  • Receptor, ErbB-2 / genetics*
  • Survival Rate
  • Time Factors

Substances

  • Biomarkers, Tumor
  • CA-125 Antigen
  • FGF3 protein, human
  • Fibroblast Growth Factor 3
  • Proto-Oncogene Proteins
  • Fibroblast Growth Factors
  • Receptor, ErbB-2