Expression of Bcl-2 and p53 protein in resectable invasive ductal carcinoma of the pancreas: Effects on clinical outcome and efficacy of adjuvant chemotherapy
Y. Nio et al., Expression of Bcl-2 and p53 protein in resectable invasive ductal carcinoma of the pancreas: Effects on clinical outcome and efficacy of adjuvant chemotherapy, J SURG ONC, 76(3), 2001, pp. 188-196
Background and Objectives: p53 tumor suppressor gene has a dual role as a t
rigger of apoptosis and as an initiator of DNA repair. The Bcl-2 can work t
o protect cells from apoptosis, which is induced by p53 gene. These facts s
uggest the significant role of these genes in the genesis and progression o
f various tumors. The present study was designed to assess the significance
of p53 and Bcl-2 protein (pBcl-2) expression on resectable invasive ductal
carcinoma (IDC) of the pancreas.
Methods: The present study included 63 IDCs, which were resected between 19
82 and 1998. pBcl-2 and p53 were stained immunohistochemically with monoclo
nal antibodies.
Results: pBcl-2 was expressed in 16 (25.4%), and p53 was positively express
ed in 32 out of 63 IDCs (50.8%); however, expression of pBcl-2, did not nec
essarily correlate with that of p53. Although p53 expression did not show a
ny significant influence on the patients' survival, pBcl-2(+) patients show
ed a higher survival than pBcl-2(-) patients for both p.53(+) and p53(-) pa
tients, which suggested that pBcl-2 expression had a more significant effec
t on the survival of patients than p53 expression. On the other hand, there
were no differences in the survival curve between the adjuvant chemotherap
y (ACT) group and the surgery alone (SA) group. pBcl-2 expression had no in
fluence on the effect of ACT, the ACT group showed a significantly better s
urvival than the SA group for p53(+) IDC patients.
Conclusions: pBcl-2 expression is a beneficial prognostic factor for patien
ts with IDC, whereas p53 expression may be beneficial in the prediction of
the effects of adjuvant chemotherapy on patients with IDC. (C) 2001 Wiley-L
iss, Inc.