Hepatic drug metabolizing enzymes were significantly decreased in Ehrl
ich ascites tumour-bearing mice. A protein inhibitor of hepatic drug m
etabolizing enzymes was isolated from Ehrlich ascites cells and purifi
ed. This involved ammonium sulphate fractionation (60-80%), DEAE, phos
phocellulose, Sephadex G-100 and hydroxyapatite column chromatography.
Purification attained was 800-fold. The inhibitory protein was effect
ive in decreasing all the components of hepatic mixed-function-oxidase
system and drug metabolizing enzymes both in vivo and in vitro. This
novel inhibitor may have potential applications in chemical carcinogen
esis. (C) 1997 Elsevier Science Ireland Ltd.