CYP3A5*3 and CYP3A4*18 single nucleotide polymorphisms in a Chinese population

被引:85
作者
Hu, YF
He, J
Chen, GL
Wang, D
Liu, ZQ
Zhang, C
Duan, LF
Zhou, HH [1 ]
机构
[1] Cent S Univ, Inst Clin Pharmacol, Pharmacogenet Res Inst, Changsha 410078, Hunan, Peoples R China
[2] Cent S Univ, Affiliated Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
CYP3A4; CYP3A5; PCR-RFLP; cytochrome P450; Chinese;
D O I
10.1016/j.cccn.2004.11.005
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Human cytochrome P450 3A evolved to catalyze the metabolism of numerous common therapy drugs and endogenous molecules. Members of the CYP3A are the majority expressed in human liver and intestine, and there are marked interindividual differences in their protein expression and activity. The activity of CYP3A enzyme in Chinese is highly variable, exceeding 14-fold, and contributes greatly to variation in oral bioavailability and systemic clearance of CYP3A substrates. The genetic factors play an important role in the interindividual variability in CYP3A activity. Detection of CYP3A5 and CYP3A4 variant alleles and knowledge about their allelic frequency in specific ethnic groups are important to lead to individualized drug dosing and improved therapeutics. Methods: We determined the allelic frequency of the CYP3A5*3 and CYP3A4*18 in a group of 302 Chinese subjects by using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assays. Results: In the group of 302 unrelated individuals, the frequency of the CYP3A5*3 and CYP3A4*18 variant allele in Chinese population were 0.778 (95% CI: 0.754, 0.802) and 0.01 (95% CI: 0, 0.02), respectively. Conclusions: We developed a simple assay for the detection of the CYP3A4* 18 allele and showed that in a Chinese population, CYP3A4*18 and CYP3A5*3 allelic frequencies are similar to that reported previously in Chinese resident in Taiwan. The frequency of the CYP3A5*3 allele in Chinese population is similar to the Japanese but lower than Caucasians. Meanwhile, our findings suggest that an approximate 62% of the Chinese population carrying CYP3A5*3/*3 genotype may appear not to express CYP3A5 protein. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:187 / 192
页数:6
相关论文
共 20 条
[1]  
AOYAMA T, 1989, J BIOL CHEM, V264, P10388
[2]   CYP3A5*3 and *6 single nucleotide polymorphisms in three distinct Asian populations [J].
Balram, C ;
Zhou, QY ;
Cheung, YB ;
Lee, EJD .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 59 (02) :123-126
[3]   GENERAL METHOD FOR ISOLATION OF HIGH MOLECULAR-WEIGHT DNA FROM EUKARYOTES [J].
BLIN, N ;
STAFFORD, DW .
NUCLEIC ACIDS RESEARCH, 1976, 3 (09) :2303-2308
[4]  
Dai D, 2001, J PHARMACOL EXP THER, V299, P825
[5]   cDNA cloning and initial characterization of CYP3A43, a novel human cytochrome p450 [J].
Domanski, TL ;
Finta, C ;
Halpert, JR ;
Zaphiropoulos, PG .
MOLECULAR PHARMACOLOGY, 2001, 59 (02) :386-392
[6]   Pharmacogenomics: Translating functional genomics into rational therapeutics [J].
Evans, WE ;
Relling, MV .
SCIENCE, 1999, 286 (5439) :487-491
[7]  
First MR, 1996, CLIN TRANSPLANT, V10, P55
[8]   Novel detection assay by PCR-RFLP and frequency of the CYP3A5 SNPs, CYP3A5*3 and *6, in a Japanese population [J].
Fukuen, S ;
Fukuda, T ;
Maune, H ;
Ikenaga, Y ;
Yamamoto, I ;
Inaba, T ;
Azuma, J .
PHARMACOGENETICS, 2002, 12 (04) :331-334
[9]   HUMAN P450PCN1 - SEQUENCE, CHROMOSOME LOCALIZATION, AND DIRECT EVIDENCE THROUGH CDNA EXPRESSION THAT P450PCN1 IS NIFEDIPINE OXIDASE [J].
GONZALEZ, FJ ;
SCHMID, BJ ;
UMENO, M ;
MCBRIDE, OW ;
HARDWICK, JP ;
MEYER, UA ;
GELBOIN, HV ;
IDLE, JR .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1988, 7 (02) :79-86
[10]   The genetic determinants of the CYP3A5 polymorphism [J].
Hustert, E ;
Haberl, M ;
Burk, O ;
Wolbold, R ;
He, YQ ;
Klein, K ;
Nuessler, AC ;
Neuhaus, P ;
Klattig, J ;
Eiselt, R ;
Koch, I ;
Zibat, A ;
Brockmöller, J ;
Halpert, JR ;
Zanger, UM ;
Wojnowski, L .
PHARMACOGENETICS, 2001, 11 (09) :773-779