Metabolic activation capacity of neonatal mice in relation to the neonatal mouse tumorigenicity bioassay

被引:14
作者
Fu, PP
Von Tungelin, LS
Hammons, GJ
McMahon, G
Wogan, G
Flammang, TJ
Kadlubar, FF
机构
[1] Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[2] MIT, Div Toxicol, Cambridge, MA 02139 USA
关键词
D O I
10.1081/DMR-100100575
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The neonatal mouse tumorigenicity bioassay is a well-developed animal model that has recently been recommended as an alternative tumorigenicity bioassay by the International Conference on Harmonization (ICH) for Technical Requirements for the Registration of Pharmaceuticals for Human Use. There are sufficient data to conclude that this animal model is highly sensitive to genotoxic chemical carcinogens that exert their tumorigenicity through mechanisms involving the formation of covalently bound exogenous DNA adducts that lead to mutation. On the other hand, it is not sensitive to chemical carcinogens that exert tumorigenicity through a secondary mechanism. The metabolizing enzymes present in the neonatal mouse, particularly the cytochromes P450, are critical factors in determining the tumorigenic potency of a chemical tested in this bioassay. However, compared to the metabolizing enzymes of the adult mouse and rat, the study of the metabolizing enzymes in neonatal mouse tissues has been relatively limited.
引用
收藏
页码:241 / 266
页数:26
相关论文
共 95 条
[21]  
FENNELL TR, 1985, CANCER RES, V45, P5310
[22]  
FLAKS ANTONIA, 1965, BRIT J CANCER, V19, P547, DOI 10.1038/bjc.1965.67
[23]   Neonatal mouse assay for tumorigenicity: Alternative to the chronic rodent bioassay [J].
Flammang, TJ ;
VonTungeln, LS ;
Kadlubar, FF ;
Fu, PP .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (02) :230-240
[24]  
FOX TR, 1990, CANCER RES, V50, P4014
[25]  
FREI JV, 1979, CANCER RES, V30, P11
[26]  
FU PF, UNPUB
[27]   COMPARATIVE REGIOSELECTIVE AND STEREOSELECTIVE METABOLISM OF 7-CHLOROBENZ[A]ANTHRACENE AND 7-BROMOBENZ[A]ANTHRACENE BY MOUSE AND RAT-LIVER MICROSOMES [J].
FU, PP ;
VONTUNGELN, LS ;
UNRUH, LE ;
NI, YC ;
CHOU, MW .
CARCINOGENESIS, 1991, 12 (03) :371-378
[28]  
Fu PP, 1998, DRUG INF J, V32, P711, DOI 10.1177/009286159803200311
[29]   Potent tumorigenicity of 7-chlorobenz[a]anthracene and 7-bromobenz[a]anthracene in the neonatal B6C3F(1) male mouse [J].
Fu, PP ;
VonTungeln, LS ;
Zhan, DJ ;
Bucci, T .
CANCER LETTERS, 1996, 101 (01) :37-42
[30]   CALORIC RESTRICTION PROFOUNDLY INHIBITS LIVER-TUMOR FORMATION AFTER INITIATION BY 6-NITROCHRYSENE IN MALE-MICE [J].
FU, PP ;
DOOLEY, KL ;
VONTUNGELN, LS ;
BUCCI, T ;
HART, RW ;
KADLUBAR, FF .
CARCINOGENESIS, 1994, 15 (02) :159-161