Background. The status of p53 protein expression was determined by imm
unohistochemistry and correlated with genetic analysis and clinical ou
tcome in patients with uterine papillary serous carcinoma (UPSC). Meth
ods. Twenty-two patients with UPSC were identified and immunohistochem
ical staining of p53 protein was performed. Staining was analyzed by q
uantitating nuclear reactivity in 500 randomly counted cells per speci
men. DNA analysis was performed on the tumors using single-strand conf
ormation polymorphism (SSCP) analysis of exons 4-10 of the p53 gene, f
ollowed by DNA sequencing of all variants. Clinical data and patient s
tatus were ascertained from chart reviews. Results. Sixteen of the 22
(73%) tumors were scored as p53-overexpressing as determined by immuno
histochemical analysis. Patients whose tumors overexpressed p53 had a
statistically significant shorter survival than those whose tumors did
not (P < 0.022). DNA analysis of the 22 tumors revealed five with mut
ations of the p53 gene. Only three of these mutations were observed in
tumors that overexpressed p53. Conclusions. A relatively large percen
tage of UPSC tumors exhibited high p53 immunoreactivity. Overexpressio
n is correlated with poor prognosis. Positive immunohistochemistry for
p53 protein in UPSC is not necessarily indicative of a genetic mutati
on.