transplantable nitrosoguanidine- induced rat colonic carcinoma was tra
nsplanted into the liver of 49 rats in six different series during thr
ee years. Tumor growth in vivo was surveyed by repeated laparotomy at
day eight and day seventeen, and 25 rats were treated with 5-fluoroura
cil (30 mg/kg body weight) once a day, between day 8 and day 17. Tumor
take was one hundred per cent and the tumor growth rate was similar t
hroughout the experimental period. No animals died due to treatment or
due to progressive tumor growth. The animals treated with 5-fluoroura
cil revealed a 5 per cent weight loss compared to the controls but no
other signs of health deterioration were observed. The tumors treated
with 5-fluorouracil had a 70 per cent decrease of growth rate compared
to control rats. Exposure of the tumor cells in vitro to 5-fluorourac
il induced a dose - related decrease in surviving cells with a 50 per
cent reduction of surviving cells 48 hours after exposure to 0.01 mg/m
l of 5-fluorouracil. Thus, we present here a new, feasible and reprodu
cible animal model, excellently suited to in vivo and in vitro studies
of fluorinated pyrimidines and solid tumor growth.