Cyclooxygenase-2 supports tumor proliferation in vestibular schwannomas

Neurosurgery. 2011 Apr;68(4):1112-7. doi: 10.1227/NEU.0b013e318208f5c7.

Abstract

Background: Recent studies have shown that cyclooxygenase-2 (COX-2) plays an important role in tumor growth and neovascularization. However, COX-2 expression in vestibular schwannomas (VSs) has not been investigated.

Objective: To analyze the pattern of COX-2 expression in sporadic and neurofibromatosis type 2 (NF2)-associated VSs and its relationship with tumor proliferation and microvessel density.

Methods: Fifteen sporadic and 15 NF2-associated VSs were examined for COX-2 expression, microvessel density, and proliferation rate by immunohistochemical methods. Immunohistochemical scores were used to interpret the extent and intensity of COX-2 staining. Microvessel density (MVD) was determined using von Willebrand factor (vWf). Proliferation rate was quantified using Ki-67. The relationship among COX-2 expression, MVD, and proliferation rate was statistically analyzed.

Results: COX-2 expression was detected in 29 (96.67%) of 30 VSs, with no significant difference between sporadic and NF2-associated VSs (P = .722). In 6 (20%) VSs, COX-2 expression was graded as strong, in 12 (40%) as moderate, and in 11 (36.7%) as weak. VSs with high proliferation showed significantly higher COX-2 expression (P = .015) than VSs with low proliferation. COX-2 expression and MVD did not show specific biological correlations (P = .035).

Conclusion: Our data demonstrate that COX-2 is expressed in VSs. High COX-2 expression in VSs with high proliferation rates suggests that the COX-2 pathway may be involved in the development and growth of VSs.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Cell Proliferation*
  • Cyclooxygenase 2 / physiology*
  • Female
  • Gene Expression Regulation, Enzymologic
  • Humans
  • Male
  • Middle Aged
  • Neovascularization, Pathologic / enzymology
  • Neovascularization, Pathologic / pathology
  • Neurofibromatosis 2 / enzymology
  • Neurofibromatosis 2 / pathology
  • Neuroma, Acoustic / enzymology*
  • Neuroma, Acoustic / pathology*
  • Young Adult

Substances

  • Cyclooxygenase 2
  • PTGS2 protein, human