R. Wada et al., HISTOGENESIS OF THE GASTRIC DIFFERENTIATED ADENOCARCINOMA-EXPRESSION OF ONCOGENE PROTEIN PRODUCTS AND MUCIN HISTOCHEMISTRY IN MINUTE GASTRIC-CANCER, Oncology Reports, 3(5), 1996, pp. 901-905
Examination of the immuno-overexpression for myc, ras, c-erbB-2 and p5
3 and the mucin histochemistry of the gastric adenocarcinoma cells at
the earlier stages were performed using 12 lesions of the well differe
ntiated tubular adenocarcinomas, less than 1 mm in greatest dimension
(G-ade-1), from the pyloric gland or the intermediate area of the surg
ically resected stomach. The G-ade-1 had a high frequency of expressio
n of oncogene myc (58%) and of the cancer suppressor gene p53 (83%), w
hile almost no expression of ras or c-erbB-2 was observed. All lesions
of G-ade-1 were positive for acid mucin staining, and 8/12 lesions (6
7%) also for sulfomucin, in 4/12 lesions (33%) gastric native mucin wa
s observed. The adjacent mucosa to all G-ade-1 lesions in this study s
howed chronic gastritis with incomplete intestinal metaplasia. These r
esults suggested that the human gastric differentiated adenocarcinoma
developed accompanying the abnormal expression of myc and p53 with ref
erence to intestinal metaplasia, and that these carcinoma cells always
had acid mucin, often the colonic native mucin as sulfomucin, and als
o sometimes gastric native mucin in the earlier stages.