W. Yasui et al., EXPRESSION OF E-CADHERIN, ALPHA-CATENINS AND BETA-CATENINS IN HUMAN GASTRIC CARCINOMAS - CORRELATION WITH HISTOLOGY AND TUMOR PROGRESSION, Oncology Reports, 2(1), 1995, pp. 111-117
The expression of cell-cell adhesion molecule, E-cadherin and its asso
ciated proteins, alpha- and beta-catenins in human gastric carcinomas
was examined by Western blotting. All the seven gastric carcinoma cell
lines expressed E-cadherin except KATOIII, which was derived from ple
ural effusion of a scirrhous type stomach cancer or Borrmann's type-4
carcinoma. The expression of alpha-catenin was not detected in HSC43 d
erived from scirrhous carcinoma, while HSC39 expressed abnormal beta-c
atenin caused by genetic alteration. In gastric carcinoma cases, the l
evels of E-cadherin and alpha-catenin were significantly lower in poor
ly differentiated adenocarcinomas and scirrhous carcinomas when compar
ed to other types of gastric carcinomas. Deeply invasive carcinomas ex
pressed E-cadherin and alpha-catenin at lower levels. However, the exp
ression level of alpha-catenin was not necessarily consistent with tha
t of E-cadherin. One of 10 gastric carcinomas examined showed complete
deletion of alpha-catenin gene in Southern blotting. beta-catenin was
expressed at lower level in poorly differentiated adenocarcinomas tha
n in well-differentiated adenocarcinomas. These findings suggest that
reduction in the expression of E-cadherin and its associated molecules
, catenins, is involved in the development and infiltrative growth of
scirrhous type gastric carcinomas.