DOSE-DEPENDENCE OF 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]-PYRIDINE (PHIP) CARCINOGENICITY IN RATS
Citation
R. Hasegawa et al., DOSE-DEPENDENCE OF 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]-PYRIDINE (PHIP) CARCINOGENICITY IN RATS, Carcinogenesis, 14(12), 1993, pp. 2553-2557
Categorie Soggetti
Oncology
SICI code
0143-3334(1993)14:12<2553:DO2(>2.0.ZU;2-Y
Abstract
The dose-dependence of 2-amino-1-methyl-6-phenylimidazo-[4,5-b]pyridin
e (PhIP) carcinogenicity was investigated in F344 rats of both sexes a
dministered title heterocyclic amine in the diet at concentrations of
25 or 100 p.p.m. for up to 104 weeks. Incidences of mammary adenocarci
nomas were 7% (2/30) for 25 p.p.m. and 47% (14 of 30 rats) for 100 p.p
.m. in females and those of colon adenocarcinomas were 43% (13/30) for
males and 13% (4/30) for females of the 100 p.p.m. groups. No mammary
adenocarcinomas were induced in males and no colon carcinomas were ob
served in the 25 p.p.m. groups of either sex. Furthermore, development
of lymphocytic leukemia was apparently enhanced by PhIP in males. In
a separate experiment, dose-dependent induction of aberrant crypts in
the large intestine, considered as preneoplastic lesions, was evident
after 8 weeks feeding of PhIP-supplemented diet at doses of 25, 100 or
400 p.p.m. Thus a clear dose-dependency was demonstrated for both col
on and mammary carcinogenesis. Since PhIP is a particularly abundant h
eterocyclic amine and its carcinogenic organotropism overlaps with the
types of neoplasias most commonly observed in western countries, the
compound may be extremely important with respect to human cancer devel
opment.