COX-2 expression in ampullary carcinoma: correlation with angiogenesis process and clinicopathological variables

J Clin Pathol. 2006 May;59(5):492-6. doi: 10.1136/jcp.2005.030098. Epub 2006 Feb 17.

Abstract

Background: There is evidence that the anti-neoplastic effect of non-steroidal anti-inflammatory drugs is attributable to cyclooxygenase-2 (COX-2) inhibition, but the exact mechanisms whereby COX-2 can promote tumour cell growth remain unclear. One hypothesis is the stimulation of tumour angiogenesis by the products of COX-2 activity. To data, there have been few clinicopathological studies on COX-2 expression in human ampullary carcinoma and no data have been reported about its relation with tumour angiogenesis.

Objective: To investigate by immunohistochemistry the expression of COX-2 and the angiogenesis process in a series of primary untreated ampullary carcinomas.

Methods: Tissue samples from 40 archival ampullary carcinomas were analysed for COX-2, vascular endothelial growth factor (VEGF), and an endothelial cell marker von Willebrand factor (vWF) by immunohistochemistry, using specific antibodies.

Results: COX-2 expression was detected in 39 tissue samples (97.5%), of which two (5%) were graded as weak, 26 (65%) as moderate, and 11 (27.5%) as strong. Only one lesion (2.5%) was negative for COX-2 expression. VEGF expression was detected in 36 tissue samples (90%). A significant positive correlation was found between COX-2 and VEGF expression. No statistic correlation was found between COX-2 expression and microvessel density.

Conclusions: COX-2 is highly expressed in ampullary carcinomas. This suggests an involvement of the COX-2 pathway in ampullary tumour associated angiogenesis, providing a rationale for targeting COX-2 in the treatment of ampullary cancer.

MeSH terms

  • Adult
  • Aged
  • Ampulla of Vater*
  • Biomarkers / analysis
  • Carcinoma / blood supply
  • Carcinoma / enzymology*
  • Common Bile Duct Neoplasms / blood supply
  • Common Bile Duct Neoplasms / enzymology*
  • Cyclooxygenase 2 / analysis*
  • Female
  • Humans
  • Immunohistochemistry / methods
  • Male
  • Middle Aged
  • Neovascularization, Pathologic / etiology*
  • Statistics, Nonparametric
  • Vascular Endothelial Growth Factor A / analysis
  • von Willebrand Factor / analysis

Substances

  • Biomarkers
  • Vascular Endothelial Growth Factor A
  • von Willebrand Factor
  • Cyclooxygenase 2