Antigrowth effect of polyamine biosynthesis inhibitors on the dunning R 3327‐G prostatic tumor

Abstract
α‐Difluoromethylornithine (DFMO) and methylglyoxal‐bis‐guanylhydrazone (MGBG), when administered simultaneously, inhibited growth and were highly toxic to the Dunning R 3327‐G hormone‐resistant prostatic adenocarcinoma transplanted into Copenhagen rats. Neither DFMO (2%) nor MGBG at a nontoxic dose (15 mg/kg) inhibited tumor growth, but total (47% early cure rate) or near total suppression of growth of established tumors was observed in rats receiving both treatments.