Abnormal expression of the 53 kDa nuclear phosphoprotein produced by t
he p53 gene is observed in many human cancers. p53 nuclear immunoreact
ivity is found commonly in tumor cells. Immunohistochemistry was perfo
rmed using a monoclonal antibody, DO-7 (DAKO, Denmark; cat. no. M7001;
1:100 dilution), to investigate p53 protein immunoreactivity; in a gr
oup of cutaneous fibrohistiocytic tumors that are known to be locally
aggressive. The study group consisted of dermatofibrosarcoma protubera
ns (DFSP) (n = 14) and atypical fibroxanthoma (AFX) (n = 7). Cases of
dermatofibroma (DF) (n = 16) formed the benign control group. Intense
nuclear immunostaining for p53 protein was observed in 71% of DFSP and
86% of AFX. None of the dermatofibromas showed strong p53 nuclear imm
unostaining. Statistical analyses revealed significant differences in
p53 immunoreactivity between DFSP and DF(P = 0.0001, chi(2) test) and
between AFX and DF (P = 0.0001, chi(2) test). In conclusion, increased
p53 protein immunoreactivity is found in DFSP and AFX but not in DF.
These differences in p53 immunoreactivity suggest that increased expre
ssion of the protein may be important in the pathogenesis of the more
aggressive group of fibrohistiocytic tumors.