Cyclooxygenase-2 expression and angiogenesis in gastric hyperplastic polyp--association with polyp size

Digestion. 2003;67(1-2):20-4. doi: 10.1159/000069708.

Abstract

Background: Cyclooxygenase (COX)-2 is the rate-limiting enzyme in prostaglandin synthesis, and plays an important role in tumor enlargement. COX-2 is expressed in human gastric and colorectal tumors, and the expression increases in a tumor size-dependent manner. In the present study, we attempted to examine the COX-2 expression pattern in gastric hyperplastic polyp, a non-tumorous lesion.

Patients and methods: Fifty-eight gastric hyperplastic polyps, obtained by endoscopic polypectomy, were immunostained with anti-COX-2 and antivascular endothelial growth factor (VEGF) antibodies. Microvessel density (MVD) was determined by von Willebrand factor immunostaining.

Results: In larger gastric hyperplastic polyps, COX-2 was expressed mainly on the luminal side of the polyp stroma, while it was absent in smaller polyps. A significant correlation between COX-2 immunoreactivity and polyp size was observed (p < 0.01). High VEGF expression and MVD were observed mainly in the same stromal region of the polyps where COX-2 was expressed. Both VEGF expression and MVD were also correlated with polyp size significantly (ps < 0.01).

Conclusions: COX-2 expression increased in a size-dependent manner in non-tumorous hyperplastic polyps, suggesting that COX-2 expression is not necessarily linked to epithelial cell transformation. Moreover, COX-2 may participate in polyp enlargement through angiogenesis by promoting VEGF production.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Cyclooxygenase 2
  • Female
  • Gastric Mucosa / blood supply
  • Gastric Mucosa / enzymology
  • Gastric Mucosa / pathology
  • Humans
  • Hyperplasia / enzymology
  • Hyperplasia / pathology
  • Isoenzymes / metabolism*
  • Male
  • Membrane Proteins
  • Middle Aged
  • Neovascularization, Pathologic / enzymology*
  • Neovascularization, Pathologic / pathology
  • Polyps / blood supply*
  • Polyps / enzymology*
  • Polyps / pathology
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Stomach Neoplasms / blood supply*
  • Stomach Neoplasms / enzymology*
  • Stomach Neoplasms / pathology

Substances

  • Isoenzymes
  • Membrane Proteins
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases