Expression of IGF-I, IGF-II, the Type-I IGF receptor and six IGF binding pr
oteins were examined in three different T-ag-driven mouse tumors. Unlike th
e widespread expression of IGF-II in pancreatic p-cell tumors, IGF-II was n
ot widely expressed in the two different pituitary tumors examined indicati
ng that a mechanism independent of focal IGF-II expression can also drive T
-antigen tumorigenesis. In addition, multiple IGF binding proteins were exp
ressed in all three tumor types. This expression, however, was generally he
terogeneous with no specific changes to indicate a required role for any IG
F binding protein in T-antigen tumorigenesis.