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Expression of vascular endothelial growth factor in renal cell carcinoma and the relation to angiogenesis and p53 protein expression
Author(s) -
Lee Ji Shin,
Kim Hyung Seok,
Jung Jong Jae,
Park Chang Soo,
Lee Min Cheol
Publication year - 2001
Publication title -
journal of surgical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.201
H-Index - 111
eISSN - 1096-9098
pISSN - 0022-4790
DOI - 10.1002/jso.1066
Subject(s) - angiogenesis , vascular endothelial growth factor , medicine , immunohistochemistry , cd34 , microvessel , cancer research , renal cell carcinoma , pathology , carcinoma , stage (stratigraphy) , vegf receptors , biology , stem cell , paleontology , genetics
Abstract Background and Objectives: Vascular endothelial growth factor (VEGF) seems to play an important role in tumor angiogenesis. The tumor‐suppressor gene p53 has been thought to regulate VEGF expression. We investigated the effect of VEGF expression on renal cell carcinoma (RCC) and the correlation between the expression of VEGF and tumor angiogenesis and p53 protein expression. Methods: Sixty‐two RCCs were examined by immunohistochemical studies with anti‐VEGF, anti‐p53, and anti‐CD34 antibodies. Results: Forty tumors (80.6%) were classified as VEGF positive, and 28 tumors (45.2%) were positive for p53 protein. The microvessel density was 75.3 ± 33.5. A significant correlation was found between VEGF expression and both the nuclear grade ( P < 0.05) and the TNM stage ( P < 0.05). The tumors with VEGF expression had a significantly higher microvessel density than those without VEGF expression ( P < 0.01). There was no statistically significant correlation between p53 protein and VEGF expression. No statistically significant differences in survival were found to be associated with microvessel density, VEGF expression or p53 protein expression. By using multivariate survival analyses, nuclear grade ( P < 0.05) and TNM stage ( P < 0.05) were the only independent prognostic factors. Conclusions: Our data do not show a direct regulation of VEGF expression by p53. We suggest that VEGF expression plays a role in the promotion of angiogenesis in RCC. J. Surg. Oncol. 2001; 77:55–60. © 2001 Wiley‐Liss, Inc.