P53 PROTEIN IMMUNOREACTIVITY IN FIBROHISTIOCYTIC TUMORS OF THE SKIN

Authors
Citation
Cs. Lee et St. Chou, P53 PROTEIN IMMUNOREACTIVITY IN FIBROHISTIOCYTIC TUMORS OF THE SKIN, Pathology, 30(3), 1998, pp. 272-275
Citations number
31
Categorie Soggetti
Pathology
Journal title
ISSN journal
00313025
Volume
30
Issue
3
Year of publication
1998
Pages
272 - 275
Database
ISI
SICI code
0031-3025(1998)30:3<272:PPIIFT>2.0.ZU;2-0
Abstract
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.