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Occludin expression decreases with the progression of human endometrial carcinoma.

Abstract
The tight junctions of the glandular epithelium are crucial for the maintenance of cell polarity, separating the plasma membrane into apical and basolateral domains. Thus abnormalities of the tight junctions may result in the structural disturbances of glandular epithelial neoplasia. In this study we introduced an anti-occludin monoclonal antibody for semiquantitative assay of the occludin expression in tissue sections of human normal and neoplastic endometrial epithelia using the Adobe Photoshop and NIH Image programs. Normal endometrial glands and samples of endometrial hyperplasia and endometrioid carcinoma grade 1 fully expressed occludin at the apical cell border. In endometrioid carcinomas grades 2 and 3, however, occludin disappeared in solid areas of the carcinomatous tissues. Occludin was also found at the apical borders of the cancer cells that formed glandular structures. Occludin expression decreased progressively in parallel with the increase in carcinoma grade, and the decreased occludin expression correlated with myometrial invasion and lymph node metastasis. These results suggest that the loss of tight junctions has a close relationship with structural atypia in the progression of human endometrial carcinomas and their malignant potential.
AuthorsHirotoshi Tobioka, Hiroshi Isomura, Yasuo Kokai, Yuichi Tokunaga, Jun Yamaguchi, Norimasa Sawada
JournalHuman pathology (Hum Pathol) Vol. 35 Issue 2 Pg. 159-64 (Feb 2004) ISSN: 0046-8177 [Print] United States
PMID14991532 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Monoclonal
  • Biomarkers, Tumor
  • Membrane Proteins
  • OCLN protein, human
  • Occludin
Topics
  • Adenocarcinoma (metabolism, pathology)
  • Adult
  • Antibodies, Monoclonal
  • Biomarkers, Tumor (immunology, metabolism)
  • Disease Progression
  • Down-Regulation
  • Endometrial Hyperplasia (metabolism, pathology)
  • Endometrial Neoplasms (metabolism, pathology)
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis
  • Membrane Proteins (immunology, metabolism)
  • Neoplasm Invasiveness
  • Occludin
  • Tight Junctions (metabolism, pathology)

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