Prognostic value of pS2 protein and receptors for epidermal growth factor (EGF-R), insulin-like growth factor-1 (IGF-1-R) and somatostatin (SS-R) in patients with breast and ovarian cancer

J Steroid Biochem Mol Biol. 1990 Dec 20;37(6):815-21. doi: 10.1016/0960-0760(90)90425-k.

Abstract

The prognostic value of EGF-R, IGF-1-R and SS-R, and of cytosolic estrogen-regulated pS2 protein, was studied in patients (pts) with primary breast and advanced ovarian cancer. Ovarian cancer tissues were negative for pS2 (by immunoradiometric assay) IGF-1-R and EGF-R contents (by ligand binding assay, LBA) were of no or moderate prognostic value for breast cancer pts (n = 214). For advanced ovarian cancer pts, EGF-R content determined by LBA (n = 55) showed no prognostic value, whereas EGF-R status (n = 35) determined by immunohistochemistry (MoAb 2E9) significantly correlated with progression of disease (P less than 0.05). In breast cancer pts, both SS-R and pS2 showed no association with tumor size, nodal status and grade. For pS2 the best cut-off level with respect to relapse-free (RFS) and overall survival (OS) was found to be 11 ng/mg protein. Both SS-R (1 g% SS-R+, n = 135; P less than 0.04) and pS2 (27% pS2+, n = 197; P less than 0.001), which were mainly positive in ER+ tumors, were of prognostic value, especially within the subgroups with ER+/PgR+ tumors. Also within N+ and No pts the 5-yr RFS and OS showed a difference between pS2+ and pS2- (33 and 54% for N+, and 31 and 13% difference for No pts). In summary, SS-R and pS2 are valuable prognosticators in breast cancer pts, and prognostic significance of EGF-R in ovarian cancer pts needs further study.

MeSH terms

  • Biomarkers, Tumor
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / metabolism*
  • ErbB Receptors / metabolism*
  • Female
  • Humans
  • Insulin-Like Growth Factor I / metabolism*
  • Neoplasm Proteins / metabolism*
  • Ovarian Neoplasms / diagnosis
  • Ovarian Neoplasms / metabolism*
  • Prognosis
  • Proteins*
  • Receptors, Cell Surface / metabolism
  • Receptors, Somatomedin
  • Trefoil Factor-1
  • Tumor Suppressor Proteins

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins
  • Proteins
  • Receptors, Cell Surface
  • Receptors, Somatomedin
  • TFF1 protein, human
  • Trefoil Factor-1
  • Tumor Suppressor Proteins
  • Insulin-Like Growth Factor I
  • ErbB Receptors