This study investigates the mdm2 gene status and expression in 66 surg
ically resected human breast carcinomas, with correlations with clinic
o-pathological and biological data (histological type, grading, steroi
d receptor status, p53 expression, proliferative activity). Four (7.7
per cent) out of 52 informative cases bear mdm2 gene amplification (fo
ur- to ten-fold) and 8 (15.4 per cent) of 52 cases showed borderline a
mplification (three-fold). Nine (13.6 per cent) out of 66 cases showed
strong mdm2 nuclear immunoreactivity. Twenty-seven (40.9 per cent) ca
ses showed isolated mdm2 reactive nuclei. All cases with clear amplifi
cation showed a high percentage of mdm2 immunoreactive nuclei. The rel
ationship between gene amplification and mdm2 protein expression is hi
ghly significant (P<0.0001). No association was observed between mdm2
gene amplification and any of the considered clinico-pathological and
biological parameters, while mdm2 immunoreactivity showed a significan
t association only with oestrogen receptor immunoreactivity (P=0.009).
p53 expression was associated neither with mdm2 gene amplification no
r with mdm2 immunoreactivity. It could be tempting to hypothesize that
the evaluation of the combined mdm2/p53 immunohistochemical phenotype
in human breast carcinoma could give us better prognostic information
than the evaluation of the expression of the p53 protein alone.