Expression of CD44 containing variant exon 9 (CD44v9) in gastric adenomas and adenocarcinomas: relation to the proliferation and progression

Int J Oncol. 1998 Jun;12(6):1253-8. doi: 10.3892/ijo.12.6.1253.

Abstract

The expression of CD44 splice variant containing exon 14 (variant exon 9: CD44v9) was examined immunohistochemically in non-neoplastic mucosa, adenoma and adenocarcinoma of the stomach and analyzed the relation with the expression of Ki-67 antigen and p53 protein. In non-neoplastic gastric mucosa, basolateral membrane of the epithelial cells in the pyloric glands showed the expression of CD44v9. The epithelial cells in the intestinal metaplastic mucosa of the stomach sometimes expressed CD44v9. In the neoplastic lesions, the expression of CD44v9 was detected in 20% (34/170) of the adenomas and 28% (132/478) of the adenocarcinomas, respectively. The incidence of CD44v9 expression did not differ among histological type of gastric carcinoma. Twelve per cent of the adenocarcinomas showed strong expression of CD44v9, whereas non of the adenomas did. The incidence of CD44v9 expression was significantly higher in carcinomas invading into muscularis propria or the cases of stages 3 and 4 in comparison with that in carcinomas limited to submucosa or the stages 1 and 2 cases (p<0.05). The incidence of positive cases was higher in carcinomas with lymph node metastasis than those without metastasis (p<0.05). The expression of CD44v9 was significantly correlated with the expression of Ki-67 (p<0.05). It was also correlated with the expression of p53 protein in the tumor cells (p<0.01). These findings overall suggest that the expression of CD44v9 may be associated with the development as well as progression of the gastric carcinomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemistry*
  • Adenocarcinoma / genetics
  • Adenocarcinoma / pathology
  • Adenoma / chemistry*
  • Adenoma / genetics
  • Adenoma / pathology
  • Biomarkers / analysis
  • Cell Division
  • Disease Progression
  • Exons / genetics
  • Gastric Fundus / chemistry
  • Gastric Mucosa / chemistry
  • Gene Expression
  • Genetic Variation / genetics
  • Humans
  • Hyaluronan Receptors / genetics*
  • Immunohistochemistry
  • Ki-67 Antigen / analysis
  • Neoplasm Staging
  • Severity of Illness Index
  • Stomach Neoplasms / chemistry*
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / pathology
  • Tumor Suppressor Protein p53 / analysis

Substances

  • Biomarkers
  • Hyaluronan Receptors
  • Ki-67 Antigen
  • Tumor Suppressor Protein p53