Mammalian cell mutagenesis of the DNA adducts of vinyl chloride and crotonaldehyde

被引:43
作者
Fernandes, PH
Kanuri, M
Nechev, LV
Harris, TM
Lloyd, RS
机构
[1] Oregon Hlth Sci Univ, Ctr Res Occupat & Environm Toxicol, Portland, OR 97239 USA
[2] Oregon Hlth Sci Univ, Dept Mol & Med Genet, Portland, OR 97239 USA
[3] Univ Texas, Med Branch, Sealy Ctr Mol Sci, Galveston, TX 77550 USA
[4] Vanderbilt Univ, Dept Chem, Nashville, TN USA
关键词
vinyl chloride; crotonaldehyde; beta-HOEdG; alpha-Me-gamma-HOPdG; mutagenicity;
D O I
10.1002/em.20117
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Vinyl chloride and crotonaldehyde are known mutagens and carcinogens that, through their reaction with DNA, form specific deoxyguanosine adducts. To investigate the mutagenic potential of a subset of the possible deoxyguanosine lesions, site-specific adducts of vinyl chloride and crotonaldehyde were synthesized, inserted into a shuttle vector, and replicated in mammalian cells. Mutation yields of the DNA adducts of vinyl chloride and crotonaldehyde were found to be 2% and 5-6%, respectively, thus suggesting that these adducts could contribute to the overall genotoxicity and carcinogenicity associated with exposure to these chemicals. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:455 / 459
页数:5
相关论文
共 33 条
[1]   Mutagenicity of site-specifically located 1,N2-ethenoguanine in Chinese hamster ovary cell chromosomal DNA [J].
Akasaka, S ;
Guengerich, FP .
CHEMICAL RESEARCH IN TOXICOLOGY, 1999, 12 (06) :501-507
[2]  
BENAMIRA M, 1992, J BIOL CHEM, V267, P22392
[3]  
Budiawan, 2000, CARCINOGENESIS, V21, P1191
[4]  
CHUNG FL, 1986, CANCER RES, V46, P1285
[5]   Endogenous formation and significance of 1,N2-propanodeoxyguanosine adducts [J].
Chung, FL ;
Nath, RG ;
Nagao, M ;
Nishikawa, A ;
Zhou, GD ;
Randerath, K .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 424 (1-2) :71-81
[6]  
Chung FL, 1999, IARC SCI PUBL, P45
[7]  
CZEMY C, 1998, MUTAT RES, V407, P125
[8]   NMR characterization of a DNA duplex containing the major acrolein-derived deoxyguanosine adduct γ-OH-1,N2-propano-2′-deoxyguanosine [J].
de los Santos, C ;
Zaliznyak, T ;
Johnson, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (12) :9077-9082
[9]   IDENTIFICATION AND CHARACTERIZATION OF DEOXYGUANOSINE CROTONALDEHYDE ADDUCTS - FORMATION OF 7,8 CYCLIC ADDUCTS AND 1,N(2),7,8 BIS-CYCLIC ADDUCTS [J].
EDER, E ;
HOFFMAN, C .
CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (06) :802-808
[10]   Mutational spectrum and genotoxicity of the major lipid peroxidation product, trans-4-hydroxy-2-nonenal, induced DNA adducts in nucleotide excision repair-proficient and -deficient human cells [J].
Feng, ZH ;
Hu, WW ;
Amin, S ;
Tang, MS .
BIOCHEMISTRY, 2003, 42 (25) :7848-7854