Sera from patients with gynaecological cancel including the ovary, endometr
ium or cervix were examined for p53 protein, using the Pantropic p53 quanti
tative ELISA. Patients with benign gynaecological pathologies were included
as a control group. p53 values ranged from undetectable to high levels of
the protein (range:0-531 pg/ml). Using the value of 200 pg/ml as the cut-of
f, p53 serum levels were found to be elevated in 23% of the patients with o
varian cancer; in 16% of the patients with endometrial cancer and in 14% of
the patients with cervical cancel: In the cona ol group, increased serum p
53 levels were found in 3.3% of patients. No differences were observed amon
g the groups with different types of cancer or at different stages, but the
differences between the cancer groups and the control group were statistic
ally significant Our results suggest that serum p53 evaluation could be an
adjunctive tool to the diagnostic laboratory tests for preoperatively gynae
cological cancers and both a competitive and alternative useful procedure f
or the detection of p53 gene mutations.