[Correlation of tissue factor expression to angiogenesis of gastric carcinoma and its clinical significance]

Ai Zheng. 2005 Jul;24(7):880-4.
[Article in Chinese]

Abstract

Background & objective: Tissue factor (TF), the primary physiologic initiator of coagulation cascade, is involved in the process of angiogenesis of various malignancies. This study was designed to investigate the correlation of TF expression to angiogenesis of gastric carcinoma, and to study its clinical significance.

Methods: The expression of TF and vascular endothelial growth factor (VEGF) in 80 specimens of gastric carcinoma and 20 specimens of normal gastric tissue was detected by EnVision immunohistochemistry. Tumor microvessel density (MVD) was evaluated using anti-CD34 antibody as an endothelial marker with the same technique as well.

Results: Positive rates of TF and VEGF, and the mean value of MVD were significantly higher in gastric carcinoma than in normal gastric tissue (65.00% vs. 5.00%, P<0.01; 67.50% vs. 5.00%, P<0.05; and 36.14+/-9.94 vs. 12.10+/-3.27, P<0.05). TF expression was positively correlated with VEGF expression and MVD value (P<0.05). TF expression was correlated to the overall survival times of patients, TNM stage, and liver metastasis (P<0.05).

Conclusion: Overexpression of TF relates with angiogenesis and prognosis of gastric carcinoma.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / blood supply
  • Adenocarcinoma / metabolism*
  • Adenocarcinoma / pathology
  • Adult
  • Aged
  • Antigens, CD34 / metabolism
  • Female
  • Follow-Up Studies
  • Humans
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / secondary
  • Lymphatic Metastasis
  • Male
  • Microcirculation / pathology
  • Middle Aged
  • Neoplasm Staging
  • Neovascularization, Pathologic*
  • Prognosis
  • Stomach Neoplasms / blood supply
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology
  • Survival Rate
  • Thromboplastin / metabolism*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Antigens, CD34
  • Vascular Endothelial Growth Factor A
  • Thromboplastin