J Korean Gastric Cancer Assoc.  2001 Mar;1(1):10-16.

Expression of p53, CD44v6 and VEGF in Gastric Adenocarcinomas

Affiliations
  • 1Department of Pathology, College of Medicine, Chung-Ang University, Seoul, Korea.

Abstract

PURPOSE: The p53 protein is a tumor supressor gene, and its mutation is associated with biologic aggressiveness. CD44v6, one of the CD44 family, is a cell surface glycoprotein that plays a role in cancer invasion and metastasis. Vascular endothelial growth factor (VEGF) is another recently identified growth factor with significant angiogenic properties. The purpose of this study was to investigate p53, CD44v6, and VEGF expressions to determine whether degree of expression was related to pathological parameters such as Lauren's classification, depth of invasion, and lymph node metastasis. MATENRIALS AND METHODS: Immunohistochemical stains of p53, CD44v6, and VEGF in formalin-fixed paraffin-embedded tissue sections of 125 gastric adenocarcinomas were done.
RESULTS
The overall expression rates of p53, CD44v6, and VEGF were 54.4% (68/125), 36.8% (46/125), and 48.0% (60/ 125), respectively. The p53, not CD44v6 and VEGF was higher in intestinal-type gastric carcinomas by Lauren's classification. The expressions of p53, CD44v6, and VEGF were statistically correlated with depth of tumor invasion. The expression of CD44v6 was higher in the lymph node metastatic group than in the negative group. The p53 expression was significantly associated with VEGF expression.
CONCLUSIONs
These data suggest that the expressions of p53, CD44v6, and VEGF are biologically related to malignancy. The p53 and CD44v6 expressions are independent; however, p53 gene mutation is one of the contributing factors to VEGF expression in gastric adenocarcinoma.

Keyword

Gastric adenocarcinoma; Immunohistochemistry; p53; CD44v6; VEGF

MeSH Terms

Adenocarcinoma*
Classification
Coloring Agents
Genes, p53
Humans
Immunohistochemistry
Lymph Nodes
Membrane Glycoproteins
Neoplasm Metastasis
Vascular Endothelial Growth Factor A*
Coloring Agents
Membrane Glycoproteins
Vascular Endothelial Growth Factor A
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