Sp. Povoski et al., TEMPORAL EXPRESSION OF THE GASTRIN (CCK-B) RECEPTOR DURING AZASERINE-INDUCED PANCREATIC CARCINOGENESIS, Pancreas, 8(5), 1993, pp. 615-621
Cholecystokinin (CCK-A) and gastrin (CCK-B) receptors have been demons
trated in the azaserine-induced rat pancreatic carcinoma DSL-6. In ord
er to determine at what stage in azaserine-induced pancreatic carcinog
enesis gastrin (CCK-B) receptors are first expressed, we examined the
binding of [I-125]gastrin-I to normal rat pancreas, azaserine-induced
premalignant pancreatic nodules, grossly normal internodular pancreas,
and DSL-6 carcinoma. We observed that specific gastrin binding was ab
sent in normal pancreas, premalignant nodules, and internodular pancre
as, and also reconfirmed our previous report of marked overexpression
of gastrin (CCK-B) receptors in the DSL-6 carcinoma. Specific cholecys
tokinin (CCK) binding was present in all pancreatic tissue types teste
d. Therefore, we conclude that the presence of gastrin (CCK-B) recepto
rs in the azaserine-induced pancreatic carcinoma DSL-6, in contrast to
their absence in premalignant nodules, suggests that the expression o
f the gastrin (CCK-B) receptor may be important in the transformation
from premalignant nodules to pancreatic cancer.