Expression of vascular endothelial growth factors (VEGF-A/VEGF-1 and VEGF-C/VEGF-2) in postmenopausal uterine endometrial carcinoma

Gynecol Oncol. 2001 Feb;80(2):181-8. doi: 10.1006/gyno.2000.6056.

Abstract

Objective: We investigated the expression of two angiogenic vascular endothelial growth factors, VEGF-A/VEGF-1 and VEGF-C/VEGF-2, in 228 cases of uterine endometrial carcinomas from postmenopausal patients to evaluate the correlation with histopathologic features and clinical outcome.

Methods: Immunohistochemistry was used to assess VEGF-A/VEGF-1 and VEGF-C/VEGF-2 expression in 228 primary surgically treated cases of postmenopausal endometrial carcinomas and the results were statistically analyzed in relation to vascular invasion, depth of invasion (myometrial vs serosal-parametrial invasion), lymphatic vessel invasion, lymph node metastasis, disease-free 5-year survival rate (DF5YR), and disease-free 10 year-survival rate (DF10YR).

Results: The results of univariate analysis showed that VEGF-A/VEGF-1 and VEGF-C/VEGF-2 expression correlated with vascular invasion (P < 0.0001, P = 0.0006), depth of invasion (P = 0.0004, P = 0.043), lymphatic vessel invasion (P = 0.021, P < 0.0001), lymph node metastasis (P = 0.0017, P = 0.0008), DF5YR (P = 0.0081, P = 0.0002), and DF10YR (P = 0.0077, P = 0.0001). Multivariate analysis showed that lymph node metastasis (P = 0.0017, P = 0.0008), parametrial-serosal invasion (P < 0.0001, P < 0.0001), and VEGF-C/VEGF-2-positive status (P = 0.03, P = 0.01) were significant factors in DF5YR and DF10YR.

Conclusions: We conclude that VEGF-A/VEGF-1 and VEGF-C/VEGF-2 expression was predictive of these histopathologic features of endometrial carcinoma and clinical outcome.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies
  • Antibody Specificity
  • Disease-Free Survival
  • Endometrial Neoplasms / blood supply
  • Endometrial Neoplasms / metabolism*
  • Endometrial Neoplasms / pathology
  • Endothelial Growth Factors / biosynthesis*
  • Endothelial Growth Factors / immunology
  • Female
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis
  • Lymphatic System / pathology
  • Middle Aged
  • Multivariate Analysis
  • Neoplasm Invasiveness
  • Postmenopause / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Risk Factors
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factor C

Substances

  • Antibodies
  • Endothelial Growth Factors
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factor C