Genetic polymorphism of CYP2E1, ADH2, and ALDH2 in Mexican-American

被引:26
作者
Wan, YJY [1 ]
Poland, RE
Lin, KM
机构
[1] Univ Calif Los Angeles, Harbor Med Ctr, Dept Pathol, Torrance, CA 90509 USA
[2] Univ Calif Los Angeles, Harbor Med Ctr, Dept Psychiat, Torrance, CA 90509 USA
来源
GENETIC TESTING | 1998年 / 2卷 / 01期
关键词
D O I
10.1089/gte.1998.2.79
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The major enzymes involved in the metabolism of ethanol are alcohol dehydrogenases (ADH) and aldehyde dehydrogenase (ALDH). Some of the isozymes of ADH are expressed polymorphically, Studies investigating a causal link between ADH expression and alcoholic liver disease (ALD) have so far produced conflicting results. The cytochrome P450 2E1 (CYP2E1) represents a second enzyme that can metabolize ethanol, Although normally a minor route of metabolism, its role in chronic alcoholics may be proportionately greater than in nonalcoholics because CYP2E1 is inducible by ethanol, An Rsa I restriction fragment length polymorphism (RFLP) in the 5'-flanking region of the CYP2E1 gene has been identified. Studies have shown that the mutant allele demonstrates greater transcriptional rate, protein level, and enzyme activity when compared with the wild-type allele, The association between the Rsa I site polymorphism and ALD has been reported. In this report, we examined the genotypes of ADH2(2), ALDH2(2), and CYP2E1 in a group of healthy subjects of Mexican-American descent, The ADH2(2) and ALDH2(2) frequencies are 6% and 0%, respectively, which are similar to those which have been reported for Caucasians. In contrast, the Rsa I allele frequency of the CYP2E1 gene is 16%, which is significantly higher than in Caucasians, The high RsaI allele frequency found in Mexican-Americans suggests that it might play a role in the development of ALD in this rapidly growing minority population where ALD is common.
引用
收藏
页码:79 / 83
页数:5
相关论文
共 40 条
[1]   GENETIC-POLYMORPHISM OF ENZYMES OF ALCOHOL METABOLISM AND SUSCEPTIBILITY TO ALCOHOLIC LIVER-DISEASE [J].
BOSRON, WF ;
LUMENG, L ;
LI, TK .
MOLECULAR ASPECTS OF MEDICINE, 1988, 10 (02) :147-158
[2]   GENETIC-POLYMORPHISM OF HUMAN-LIVER ALCOHOL AND ALDEHYDE DEHYDROGENASES, AND THEIR RELATIONSHIP TO ALCOHOL METABOLISM AND ALCOHOLISM [J].
BOSRON, WF ;
LI, TK .
HEPATOLOGY, 1986, 6 (03) :502-510
[3]   POLYMORPHISM AT THE P4501IE1 LOCUS IS NOT ASSOCIATED WITH ALCOHOLIC LIVER-DISEASE IN CAUCASIAN MEN [J].
CARR, LG ;
HARTLEROAD, JY ;
LIANG, YB ;
MENDENHALL, C ;
MORITZ, T ;
THOMASSON, H .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1995, 19 (01) :182-184
[4]   ALCOHOL-INDUCIBLE CYTOCHROME-P-450 (P-450ALC) [J].
COON, MJ ;
KOOP, DR .
ARCHIVES OF TOXICOLOGY, 1987, 60 (1-3) :16-21
[5]   HUMAN-LIVER MICROSOMAL CYTOCHROME-P-450IIE1 - IMMUNOLOGICAL EVALUATION OF ITS CONTRIBUTION TO MICROSOMAL ETHANOL OXIDATION, CARBON-TETRACHLORIDE REDUCTION AND NADPH OXIDASE ACTIVITY [J].
EKSTROM, G ;
VONBAHR, C ;
INGELMANSUNDBERG, M .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (04) :689-693
[6]   Chlormethiazole inhibition of cytochrome P450 2E1 as assessed by chloroxazone hydroxylation in humans [J].
Gebhardt, AC ;
Lucas, D ;
Menez, JF ;
Seitz, HK .
HEPATOLOGY, 1997, 26 (04) :957-961
[7]  
GOEDDE HW, 1979, HUM GENET, V51, P331
[8]  
GONZALEZ FJ, 1988, PHARMACOL REV, V40, P243
[9]  
GUENGERICH FP, 1991, MOL DOSIMETRY HUMAN, P27
[10]  
HARADA S, 1993, ALCOHOL ALCOHOLISM, V28, P11