Transforming growth Factor-β (TGF-β) bind to the type II TGF-P receptor (TβRII), which then heterodimer-izes with the type I TGF-β receptor (TβRI), thereby initiating a signaling cascade. TGF-β are overexpressed in pancreatic cancer, and this overexpression is associated with more aggressive disease. Although TβR II also is overexpressed in pancreatic ductal adenocarcinoma cells in vivo, the biologic significance of this overexpression is not completely known. Therefore in this study, we characterized TβR II expression by Northern blot analysis in 32 normal and 42 cancerous pancreatic tissues and correlated the survival of the cancer patients with TβR II messenger RNA (mRNA) levels. Northern blot analysis revealed that, by comparison with the normal controls, TPRII expression was increased in 19 (45%) of 42 cancer samples. Densitometric analysis of all the pancreatic tissues revealed a 3.4-fold increase (p< 0.01) in TβRII mRNA levels in the cancer tissues by comparison with normal controls. There was a strong correlation between the expression of TβRII and the levels of two invasion-promoting genes, plasminogen-activator-inhibitor-1 (PAI-1) and matrix-metalloproteinase-9 (MMP9). Log-rank analysis of the Kaplan-Meier survival curves indicated that patients whose tumors overexpressed TβRII had a significantly shorter survival period than did patients whose cancers expressed low levels of TβRII. It is suggested that TβRII overexpression may be a marker that correlates with disease progression in pancreatic ductal adenocarcinoma.