Chemical and biological factors affecting mutagen potency

被引:39
作者
Colvin, ME [1 ]
Hatch, FT [1 ]
Felton, JS [1 ]
机构
[1] Univ Calif Lawrence Livermore Natl Lab, Biol & Biotechnol Res Program, Livermore, CA 94550 USA
关键词
aromatic amine mutagen; food mutagen; review; quantitative structure-activity relationship; computational chemistry;
D O I
10.1016/S0027-5107(98)00073-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This review surveys the chemical and biological factors that are correlated with the mutagenic activity of the aromatic and heterocyclic amines, Particular attention is given to the predicted quantum chemical properties of the parent amines and their metabolites. A number of chemical properties have been found to correlate well with measured mutagenic potency, including log P, the energies of the frontier orbitals of the parent amines, and the thermodynamic stability of the nitrenium ion, possibly the ultimate DNA-binding species. These correlations are intriguing clues to the mutagenic activity of the aromatic amines; however, many factors still await final explanation, including the exact mechanisms of the metabolic enzymes, the identity(s) of the ultimate DNA-binding species, the reaction mechanism in the DNA-adduction, the role of sequence context in the covalent and non-covalent binding of the adducts, and the role of DNA repair. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:479 / 492
页数:14
相关论文
共 73 条
[1]   REPAIR OF UV-DAMAGED DNA BY MAMMALIAN-CELLS AND SACCHAROMYCES-CEREVISIAE [J].
ABOUSSEKHRA, A ;
WOOD, RD .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (02) :212-220
[2]  
[Anonymous], UPD IARC MON
[3]   QUANTITATIVE STRUCTURE ACTIVITY RELATIONSHIPS - PRINCIPLES, AND APPLICATIONS TO MUTAGENICITY AND CARCINOGENICITY [J].
BENIGNI, R ;
ANDREOLI, C ;
GIULIANI, A .
MUTATION RESEARCH, 1989, 221 (03) :197-216
[4]   KINETICS AND MECHANISM OF THE DECOMPOSITION IN AQUEOUS-SOLUTIONS OF 2-(HYDROXYAMINO)IMIDAZOLES [J].
BOLTON, JL ;
MCCLELLAND, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (21) :8172-8181
[5]   BIOACTIVATION OF N-HYDROXY-2-ACETYLAMINOFLUORENES BY N,O-ACYLTRANSFERASE - SUBSTITUENT EFFECTS ON COVALENT BINDING TO DNA [J].
BOTEJU, LW ;
HANNA, PE .
CARCINOGENESIS, 1993, 14 (08) :1651-1657
[6]   ARYLAMINE-NUCLEOSIDE ADDUCT FORMATION - EVIDENCE FOR ARYLNITRENE INVOLVEMENT IN THE REACTIONS OF AN N-ACETOXYARYLAMINE [J].
BOTEJU, LW ;
HANNA, PE .
CHEMICAL RESEARCH IN TOXICOLOGY, 1994, 7 (05) :684-689
[7]  
BUTLER MA, 1989, CANCER RES, V49, P25
[8]   Review of mutagenicity of monocyclic aromatic amines: quantitative structure-activity relationships [J].
Chung, KT ;
Kirkovsky, L ;
Kirkovsky, A ;
Purcell, WP .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 1997, 387 (01) :1-16
[9]   FRONTIER ORBITAL ENERGIES IN QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS - A COMPARISON OF QUANTUM-CHEMICAL METHODS [J].
CLARE, BW .
THEORETICA CHIMICA ACTA, 1994, 87 (06) :415-430
[10]  
Clark T. A., 1985, Handbook of Computational Chemistry