Cell adhesion molecules in bladder cancer: Soluble serum E-cadherin correlates with predictors of recurrence

  • T. R.L. Griffiths
  • , I. Brotherick
  • , R. I. Bishop
  • , M. D. White
  • , D. M. McKenna
  • , C. H.W. Horne
  • , B. K. Shenton
  • , D. E. Neal
  • , J. K. Mellon

Research output: Contribution to journalArticlepeer-review

86 Scopus citations

Abstract

Sera from 40 patients with newly diagnosed bladder cancer (28 superficial tumours (pTa and pT1) and 12 muscle-invasive tumours) were assessed by enzyme-linked immunosorbent assay (ELISA) to determine the concentrations of soluble E-cadherin (sE-cadherin), soluble E-selectin (sE-selectin), soluble vascular cell adhesion molecule-1 (sVCAM-1) and soluble intercellular adhesion molecule-1 (sICAM-1). Corresponding frozen sections of primary tumour were analysed for E-cadherin expression using the monoclonal antibody, HECD-1 and standard immunohistochemistry. Patients with bladder cancer had significantly higher concentrations of sE-cadherin compared with a control group (P = 0.017). No difference was found between the two groups with regard to sE-selectin (P = 0.403), sVCAM-1 (P = 0.942) and sICAM-1 (P = 0.092). High levels of sE-cadherin were related to poor histological grade (P=0.009), number of superficial tumours at presentation (P = 0.008) and a positive 3 month check cytoscopy in superficial disease (P = 0.036). Abnormal E-cadherin expression was associated with increasing tumour stage (P = 0.009) and grade (P = 0.03). There was no correlation between high levels of soluble E-cadherin in sera and abnormal E-cadherin expression by the tumour (P = 0.077). Elevated levels of sE-cadherin are found in sera of patients with bladder cancer and correlate with known prognostic factors.

Original languageEnglish
Pages (from-to)579-584
Number of pages6
JournalBritish Journal of Cancer
Volume74
Issue number4
DOIs
StatePublished - 1996
Externally publishedYes

Keywords

  • Bladder neoplasm
  • Cell adhesion molecule
  • Enzyme-linked immunosorbent assay
  • Immunohistochemistry

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