Two major xenobiotic metabolizing sub-families of cytochrome P450 (cyt
ochrome P450 IA and cytochrome P450 3A) have been identified in soft t
issue sarcomas. Cytochrome P450 1A was present in 70 per cent and cyto
chrome P450 3A was present in 78 per cent of tumours, respectively. A
high proportion (86 per cent) of those tumours which contained cytochr
ome P450 1A or cytochrome P450 3A demonstrated co-expression of both s
ub-families. In each tumour, cytochrome P450 immunoreactivity was iden
tified in all tumour cells and there was no intra-tumour heterogeneity
. These results indicate that expression of cytochrome P450 is a commo
n molecular event in soft tissue sarcomas and that the presence of dif
ferent sub-families of cytochrome P450 has implications both for the p
athogenesis and for the treatment of these tumours. Cytochrome P450 ex
pression may influence the intrinsic drug resistance of these tumours
and also provide a molecular target for anti-cancer drugs which can be
activated by cytochrome P450.