Abstract
The function of E-cadherin is thought to be regulated by its associated cytoplasmic proteins including alpha-catenin. To determine whether possible downregulation of alpha-catenin expression may play a role in tumor invasion and metastasis through the dysfunction of E-cadherin, we investigated the expression of alpha-catenin in human carcinoma samples (esophagus, stomach, and colon) by immunohistochemistry using our monoclonal antibody against alpha-catenin (alpha-18). Normal epithelium expressed alpha-catenin strongly without exception. However, alpha-catenin expression was frequently reduced in primary tumors of esophagus (12 of 15:80%), stomach (14 of 20: 70%), and colon (8 of 10: 80%). Of the tumors with reduced alpha-catenin expression, alpha-catenin expression was completely negative in 70.6% of them (9 of 12 in esophagus, 9 of 14 in stomach, and 6 of 8 in colon). These results also suggested that some human cancer cells may have impaired E-cadherin-mediated cell adhesiveness through the downregulation of alpha-catenin expression.
MeSH Terms
Adenocarcinoma/metabolism,pathology
Adult
Aged
Cadherins/metabolism
Carcinoma, Squamous Cell/metabolism,pathology
Colonic Neoplasms/metabolism,pathology
Cytoskeletal Proteins/metabolism
Down-Regulation
Esophageal Neoplasms/metabolism,pathology
Female
Humans
Immunoenzyme Techniques
Infant
Male
Middle Aged
Neoplasm Staging
Stomach Neoplasms/metabolism,pathology
alpha Catenin
Chemicals
CTNNA1 protein, human
Cadherins
Cytoskeletal Proteins
alpha Catenin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Shiozaki H
Department of Surgery II, Osaka University Medical School, Japan.
Iihara K
Oka H
Kadowaki T
Matsui S
Gofuku J
Inoue M
Nagafuchi A
Tsukita S
Mori T
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