The hypoxia-inducible genes VEGF and CA9 are differentially regulated in superficial vs invasive bladder cancer

K. J. Turner, J. P. Crew, C. C. Wykoff, P. H. Watson, R. Poulsom, J. Pastorek, P. J. Ratcliffe, D. Cranston, A. L. Harris

Research output: Contribution to journalArticle

102 Scopus citations

Abstract

Regulation by hypoxia may underlie the expression of vascular endothelial growth factor in bladder cancer. We have compared the distribution of vascular endothelial growth factor mRNA with a hypoxia marker, carbonic anhydrase 9 (CA IX). vascular endothelial growth factor mRNA was analysed by in situ hybridisation and CA IX by immunochemistry in 22 cases of bladder cancer. The relationship of microvessels to the distribution of CA IX was determined. In a separate series of 49 superficial tumours, CA IX immunostaining was compared with clinico-pathological outcome. In superficial and invasive disease there was overlap in the expression of vascular endothelial growth factor and CA IX, CA IX being more widespread. Both were expressed predominantly on the luminal surface, and surrounding areas of necrosis (invasive tumours). Expression of both factors was greater in superficial disease. Expression was absent within ∼80 μm of microvessels. Unlike vascular endothelial growth factor, CA IX did not predict outcome in superficial disease. Differential responses to reoxygenation provide one explanation: vascular endothelial growth factor mRNA declined rapidly, while CA IX expression was sustained for >72 h. Expression of vascular endothelial growth factor mRNA in bladder tumours is consistent with hypoxic regulation and suggests differential regulation in superficial vs invasive disease. The expression of CA IX on the luminal surface justifies investigation of its utility as a therapeutic target/prognostic indicator.

Original languageEnglish (US)
Pages (from-to)1276-1282
Number of pages7
JournalBritish Journal of Cancer
Volume86
Issue number8
DOIs
StatePublished - 2002

Keywords

  • Angiogenic factors
  • Bladder neoplasms
  • Carbonic acid
  • Cell hypoxia

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

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