A. Sakamoto et al., H-, K-, and N-ras gene mutation in atypical fibroxanthoma and malignant fibrous histiocytoma, HUMAN PATH, 32(11), 2001, pp. 1225-1231
Citations number
36
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Atypical fibroxanthoma (AFX) which is histologically similar to malignant f
ibrous histiocytoma (MFH), occurs in the sun-exposed skin. The presence of
mutations at codons 12 and 13 of the H- and K-ras genes and in exons 1 and
2, which include codons 12, 13, and 61, of the N-ras gene was studied in 8
cases of AFX and 8 cases of storiform-pleomorphic-type MFH using polymerase
chain reaction (PCR)-restriction fragment length polymorphism and PCR-sing
le-conformation polymorphism. Two of the 8 cases of NIM showed ras mutation
s in the H-ras gene at codon 12 (GGC-AGC) and in the K-ras gene at codon 13
(GGC-GAC). H- and K-ras gene mutations were not seen in any of the cases o
f AIX (0 of 8). N-ras gene mutation was not detected in either the AFX (0 o
f 8) or MFH (0 of 8) cases. In conclusion, although the number of cases in
this study was small, H-and K-ras genes were present in some of the MFH cas
es and accordingly may play an important role in the pathogenesis of MFH. I
n addition, the finding that H-, K-, and N-ras gene mutations are not prese
nt in AIX may indicate why AFX has a more favorable behavior than MFH. HUM
PATHOL 32:1225-1231. Copyright (C) 2001 by W.B. Saunders Company.