Alteration of the tumour-suppressor gene p53 is the commonest genetic
change encountered in human malignant tumours. A study was undertaken
to ascertain the prognostic value of p53 immunoexpression in nephrobla
stomas. A series of 93 consecutive cases was analysed. Archival formal
in-fixed, paraffin wax-embedded tissue sections were stained with mono
clonal anti-p53 antibody (DO-7, Dako) using a peroxidase-labelled stre
ptavidin biotin kit. Five of seven tumours (71.4%) with unfavourable h
istology, but only 3 of 86 favourable histology tumours, showed 'high'
p53 immunoexpression (P < 0.001). p53 expression in unfavourable hist
ology tumours was present in both anaplastic and non-anaplastic compon
ents. Moreover, there was uniform staining of blastema, epithelium and
stroma in unfavourable histology tumours. No statistical difference i
n p53 expression was found between patients who had received and those
who had not received preoperative chemotherapy (P = 0.678). Similarly
, no statistical difference was found in the groups of patients who we
re disease free, who had residual/recurrent disease or who had died (P
= 0.238). The mean survival period for patients with tumours that had
'low' and 'high' expressions was 24.8 months and 12.6 months respecti
vely (P = 0.0003). In conclusion, p53 immunoexpression in nephroblasto
mas was found to be an important determinant of poor prognosis as it i
dentifies those patients with a shorter survival period and also those
with unfavourable histology tumours. It may also be of practical valu
e to the practising pathologist by identifying those tumours that requ
ire careful assessment for the presence of anaplasia.