Evidence of association of the CYP2E1 genetic polymorphism with micronuclei frequency in human peripheral blood

被引:20
作者
Ishikawa, H
Yamamoto, H
Tian, Y
Kawano, M
Yamauchi, T
Yokoyama, K
机构
[1] Mie Univ, Sch Med, Dept Publ Hlth & Prevent Med, Tsu, Mie 5148507, Japan
[2] Mie Univ, Sch Med, Dept Forens Med & Sci, Tsu, Mie 5148507, Japan
[3] Mie Univ, Sch Med, Dept Microbiol, Tsu, Mie 5148507, Japan
[4] Shanghai Med Univ 2, Sch Publ Hlth, Shanghai 200025, Peoples R China
关键词
age; alcohol; CYP2E1; polymorphism; micronuclei; odds ratio; RsaI;
D O I
10.1016/j.mrfmmm.2003.10.007
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
Micronuclei (MN) are used as one of the cytogenetic biomarkers, and intra- and inter-individual variations in this frequency have been reported in human blood lymphocytes. Polymorphisms in a few metabolic enzyme genes seem to account for a proportion of this variability, but the impacts of specific genetic variants on the MN frequency have not yet been clarified. Here, we investigated the relationship between the MN frequency and several gene polymorphisms in 90 healthy Japanese men. The subjects with the CYP2E1*3 variant allele had a statistically lower mean MN frequency than subjects with the CYP2E1*1/*1 wild type. Furthermore, the adjusted odds ratio (OR) of the CYP2E1*3 variant with higher MN frequency levels was also significantly lower and calculated to be 0.25 (95% CI 0.07-0.83), when the OR for the subjects with the CYP2E1*1/*1 wild type was defined as 1.00. These data suggest that the CYP2E1*3 polymorphism may have the potential to influence the baseline frequency of MN. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 53
页数:9
相关论文
共 33 条
[1]  
Bolognesi C, 1997, CANCER EPIDEM BIOMAR, V6, P249
[2]   Biomonitoring of exposure to urban air pollutants: analysis of sister chromatid exchanges and DNA lesions in peripheral lymphocytes of traffic policemen [J].
Carere, A ;
Andreoli, C ;
Galati, R ;
Leopardi, P ;
Marcon, F ;
Rosati, MV ;
Rossi, S ;
Tomei, F ;
Verdina, A ;
Zijno, A ;
Crebelli, R .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 518 (02) :215-224
[3]   Exposure to epichlorohydrin and dimethylformamide, glutathione S-transferases and sister chromatid exchange frequencies in peripheral lymphocytes [J].
Cheng, TJ ;
Hwang, SJ ;
Kuo, HW ;
Luo, JC ;
Chang, MJW .
ARCHIVES OF TOXICOLOGY, 1999, 73 (4-5) :282-287
[4]   Micronuclei in blood lymphocytes and genetic polymorphism for GSTM1, GSTT1 and NAT2 in pesticide-exposed greenhouse workers [J].
Falck, GCM ;
Hirvonen, A ;
Scarpato, R ;
Saarikoski, ST ;
Migliore, L ;
Norppa, H .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1999, 441 (02) :225-237
[5]  
FENCH M, 1999, MUTAT RES, V428, P271
[6]   The in vitro micronucleus technique [J].
Fenech, M .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2000, 455 (1-2) :81-95
[7]   THE CYTOKINESIS-BLOCK MICRONUCLEUS TECHNIQUE - A DETAILED DESCRIPTION OF THE METHOD AND ITS APPLICATION TO GENOTOXICITY STUDIES IN HUMAN-POPULATIONS [J].
FENECH, M .
MUTATION RESEARCH, 1993, 285 (01) :35-44
[8]  
Guengerich FP, 1998, MUTAT RES-FUND MOL M, V400, P201
[9]   PCR DETECTION OF AN A/G POLYMORPHISM WITHIN EXON-7 OF THE CYP1A1 GENE [J].
HAYASHI, SI ;
WATANABE, J ;
NAKACHI, K ;
KAWAJIRI, K .
NUCLEIC ACIDS RESEARCH, 1991, 19 (17) :4797-4797
[10]   The glutathione S-Transferase supergene family: Regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance [J].
Hayes, JD ;
Pulford, DJ .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 30 (06) :445-600