Conclusion: Anti-p53-autoantibodies (a-p53-aabs) may suppress the deve
lopment of distant metastases, but not lymph node metastases, This cou
ld explain the significantly prolonged survival of patients with UICC
stage III tumors who have a-p53-aabs compared to those without a-p53-a
abs. Background: Mutation within the tumor suppressor gene p53 leads t
o increased intracellular p53 protein levels and an increased antibody
formation against this molecule. Altered p53 has been proposed to be
associated with poor prognosis, and the present study investigated whe
ther the detection of a humoral response to p53 gives evidence for a p
rognostic or diagnostic parameter in pancreatic disorders. Methods: We
screened 145 patients with pancreatic cancer and 95 patients with chr
onic pancreatitis for the development of a-p53-aab via ELISA and Weste
rn-blotting. p53 expression was examined by immuno-histochemistry. Res
ults: We found that 41% of the tissues of patients suffering from panc
reatic carcinoma overexpressed p53, and 15.9% of the patients sufferin
g from pancreatic cancer developed a-p53-aab. In pancreatic cancer, we
could exhibit a significant correlation between grading, p53-overexpr
ession, survival, and antibody response against p53. A-p53-aabs were s
ignificantly more frequent in patients with stage III tumors (tumors w
ith lymph node metastases, but not distant metastases, p < 0.02).