Co-ordinated changes in expression of cell adhesion molecules in prostate cancer

S J Murant, J Handley, M Stower, N Reid, O Cussenot, N J Maitland

Research output: Contribution to journalArticlepeer-review

Abstract

The expressions of E-cadherin, the integrin subunits beta(1), beta(2), beta(3), CD44 and alpha-catenin were studied in parallel by immunohistochemistry in a series of 40 prostate biopsies comprising one normal, 11 benign prostatic hyperplasia (BPH), and 28 prostatic adenocarcinomas. As reported by others, there was a consistent loss of E-cadherin expression with increasing tumour grade and de-differentiation. However, a significant proportion of losses occurred at earlier grades than previously reported. The parallel nature of this study showed, for the first time in human prostate carcinoma, a reciprocal expression pattern of E-cadherin and beta(1) integrin in the higher grades of prostate cancer. A reciprocal expression pattern was also found for E-cadherin and CD44 between moderately and poorly differentiated tumours. alpha-Catenin expression was downregulated only in those cells which had previously lost E-cadherin expression, and beta(2) and beta(3) integrin were rarely expressed in prostate tumours. A loss of expression of the luminal epithelial specific keratins CK8 and CK18 was also observed in advanced stage, poorly differentiated carcinomas. (C) 1997 Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)263-271
Number of pages9
JournalEuropean Journal of Cancer
Volume33
Issue number2
Publication statusPublished - Feb 1997

Keywords

  • prostate cancer
  • adhesion molecules
  • integrin
  • cadherin
  • catenin
  • CD44
  • E-CADHERIN
  • DIFFERENTIAL EXPRESSION
  • NEOPLASTIC PROSTATE
  • GENETIC CHANGES
  • METASTASIS
  • INTEGRINS
  • CARCINOMA
  • PROTEINS
  • LINES

Cite this