Uroplakin gene expression in normal human tissues and locally advanced bladder cancer

J Olsburgh, P Harnden, R Weeks, B Smith, A Joyce, G Hall, R Poulsom, P Selby, J Southgate

Research output: Contribution to journalArticlepeer-review

Abstract

The uroplakins are widely regarded as urothelium-specific markers of terminal urothelial cytodifferentiation. This study investigated the expression of the four uroplakin genes, UPIa, UPIb, UPII and UPIII, in a wide range of normal human tissues to determine tissue specificity and in advanced transitional cell carcinoma (TCC) to examine gene expression in primary and metastatic disease. In the urinary tract, all four uroplakins were expressed by urothelium and UPIII was also expressed by prostatic glandular epithelium. UPIa and UPII appeared to be urothelium-specific, but UPIb was detected in several non-urothelial tissues, including the respiratory tract, where it was associated with squamous metaplasia of tracheal and bronchial epithelia. The ten cases of primary TCC and corresponding lymph node metastases demonstrated that each uroplakin gene could be expressed at the mRNA level. No single uroplakin gene was expressed in all primary tumours or metastases, but 80% of the primary tumours and 70% of the lymph node metastases expressed at least one uroplakin gene. UPIII mRNA was often expressed in the absence of UPIII protein. These results confirm that in human tissues the expression of UPIa and UPII genes is highly specific to urothelium and suggest that the tight differentiation-restricted expression of uroplakin genes in normal urothelium is lost following malignant transformation.
Original languageEnglish
Pages (from-to)41-49
Number of pages8
JournalJournal of Pathology
Volume199
Issue number1
DOIs
Publication statusPublished - Jan 2003

Keywords

  • urothelium
  • bladder cancer
  • transitional cell carcinoma
  • metastasis
  • differentiation
  • uroplakin
  • gene expression
  • in situ hybridization
  • TRANSITIONAL-CELL CARCINOMA
  • LYMPH-NODE METASTASIS
  • IN-SITU HYBRIDIZATION
  • PERIPHERAL-BLOOD
  • UROTHELIAL CELLS
  • MESSENGER-RNA
  • PROTEINS
  • MARKER
  • IB
  • CYTOKERATIN-20

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