INDUCTION OF THE P-450-I FAMILY OF PROTEINS BY POLYCYCLIC AROMATIC-HYDROCARBONS - POSSIBLE RELATIONSHIP TO THEIR CARCINOGENICITY

被引:37
作者
AYRTON, AD
MCFARLANE, M
WALKER, R
NEVILLE, S
COOMBS, MM
IOANNIDES, C
机构
[1] UNIV SURREY,DEPT BIOCHEM,GUILDFORD GU2 5XH,SURREY,ENGLAND
[2] UNIV SURREY,DEPT CHEM,IMPERIAL CANC RES FUND LAB,GUILDFORD GU2 5XH,SURREY,ENGLAND
关键词
Chemical carcinogenesis; Cytochrome P-450; Enzyme induction; Mixed-function oxidases; Polycyclic aromatic hydrocarbons;
D O I
10.1016/0300-483X(90)90171-C
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The hypothesis has been put forward that mutagenic polycyclic aromatic hydrocarbons which induce the P-450 I family of cytochromes, the major enzyme system responsible for their activation, are likely to be carcinogenic. In order to test this hypothesis, rats have been pretreated with a number of polycyclic aromatic hydrocarbons of different mutagenic and carcinogenic potency and hepatic P-450 I activity was monitored using chemical probes such as the O-deethylation of ethoxyresorufin and metabolic activation of Glu-P-1 to mutagens, and immunologically employing polyclonal antibodies against purified rat P-450 I A1. All compounds studied enhanced P-450 I activity and induced P-450 I apoproteins but the extent of induction was very markedly different. The results are discussed with reference to the mutagenicity of these chemicals in the Ames test and their carcinogenicity in the classical mouse skin model. A relationship appears to exist between carcinogenicity of polycyclic aromatic hydrocarbons and their ability to induce hepatic P-450 I activity. © 1990.
引用
收藏
页码:173 / 186
页数:14
相关论文
共 56 条
[1]   INDUCTION OF DIFFERENT ISOZYMES OF CYTOCHROME-P-450 AND OF MICROSOMAL EPOXIDE HYDROLASE IN RAT-LIVER BY 2-ACETYLAMINOFLUORENE AND STRUCTURALLY RELATED-COMPOUNDS [J].
ASTROM, A ;
BIRBERG, W ;
PILOTTI, A ;
DEPIERRE, JW .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 154 (01) :125-134
[2]   METABOLISM OF 2-ACETYLAMINOFLUORENE BY 8 DIFFERENT FORMS OF CYTOCHROME-P-450 ISOLATED FROM RAT-LIVER [J].
ASTROM, A ;
DEPIERRE, JW .
CARCINOGENESIS, 1985, 6 (01) :113-120
[3]   INDUCTION OF THE RAT HEPATIC-MICROSOMAL MIXED-FUNCTION OXIDASES BY 2 AZA-ARENES - A COMPARISON WITH THEIR NON-HETEROCYCLIC ANALOGS [J].
AYRTON, AD ;
TRINICK, J ;
WOOD, BP ;
SMITH, JN ;
IOANNIDES, C .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (23) :4565-4571
[4]  
BENEDICT WF, 1973, MOL PHARMACOL, V6, P266
[5]  
BHATT TS, 1983, CANCER RES, V43, P984
[6]   CARCINOGENICITY AND MUTAGENICITY OF SOME ALKOXY CYCLOPENTA[A]-PHENANTHREN-17-ONES - EFFECT OF OBSTRUCTING THE BAY REGION [J].
BHATT, TS ;
HADFIELD, ST ;
COOMBS, MM .
CARCINOGENESIS, 1982, 3 (06) :677-680
[7]   ETHOXYPHENOXAZONES, PENTOXYPHENOXAZONES, AND BENZYLOXYPHENOXAZONES AND HOMOLOGS - A SERIES OF SUBSTRATES TO DISTINGUISH BETWEEN DIFFERENT INDUCED CYTOCHROMES-P-450 [J].
BURKE, MD ;
THOMPSON, S ;
ELCOMBE, CR ;
HALPERT, J ;
HAAPARANTA, T ;
MAYER, RT .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (18) :3337-3345
[8]  
BURKE MD, 1974, DRUG METAB DISPOS, V2, P583
[9]  
COOMBS MM, 1976, CANCER RES, V36, P4525
[10]   CARCINOGENICITY OF 15,16-DIHYDRO-11-METHYL-CYCLOPENTA[A]PHENANTHREN-17-ONE [J].
COOMBS, MM ;
BHATT, TS ;
YOUNG, S .
BRITISH JOURNAL OF CANCER, 1979, 40 (06) :914-921