The expression of the nuclear protein p53 in oligodendrogliomas was in
vestigated by immunohistochemistry, using a monoclonal anti-p53 antibo
dy (DO-7) on formalin-fixed, paraffin-embedded material in 84 histolog
ically verified cases, and compared with the histopathological grade a
nd survival. p53-immunoreactive cells were found in 75 per cent of the
samples acquired at the first biopsy. The p53 labelling index was not
related to the degree of nuclear anaplasia. Tumour cases with more th
an 75 per cent p53 immunostained cells had a rapidly fatal clinical co
urse. However, no significant correlation was found between p53 labell
ing index and tumour grade, mitotic index, or ploidy status. In most t
umour recurrences (n=25), the p53 labelling index increased or remaine
d at the level of the first biopsy. In five cases (6 per cent), p53 wa
s absent in the first sample as well as in the recurrence. Irrespectiv
e of the underlying aberration of either the gene or the metabolic pat
hway of p53, it is concluded that a high percentage (i.e., more than 7
5 per cent) of p53-immunolabelled cells is predictive of an unfavourab
le clinical course, while a percentage lower than 75 per cent immunore
active cells does not exclude a rapid fatal outcome.