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Simultaneous detection of CYP3A5 and MDR1 polymorphisms based on the SNaPshot assay
被引:8
|作者:
Li, Liang
[2
]
Li, Chuan-Jiang
[1
]
Zhang, Yan-Jun
[3
]
Zheng, Lei
Jiang, Hai-Xia
Si-Tu, Bo
机构:
[1] So Med Univ, Nanfang Hosp, Dept Organ Transplantat, Guangzhou 510515, Guangdong, Peoples R China
[2] So Med Univ, Sch Basic Med Sci, Guangzhou 510515, Guangdong, Peoples R China
[3] Univ Cincinnati, Coll Pharm, Acad Hlth Ctr, Cincinnati, OH 45267 USA
关键词:
CYP3A5;
MDR1;
SNP;
Genotyping;
Sequencing;
SINGLE-NUCLEOTIDE POLYMORPHISMS;
P-GLYCOPROTEIN;
GENETIC POLYMORPHISMS;
PHARMACOKINETICS;
DISPOSITION;
C3435T;
PCR;
GENOTYPES;
G2677T/A;
C1236T;
D O I:
10.1016/j.clinbiochem.2010.12.018
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: The 6986A > G polymorphism for CYP3A5 and the -129T > C, 1236C > T, 2677G > T/A, and 3435C > T polymorphisms for MDR1 are considered the major genetic factors affecting a range of drugs' metabolism and transport. Simultaneous genotyping of these five polymorphisms would be useful for estimating the therapeutic effects of their related drugs. Subjects and methods: We have described a SNaPshot assay that can simultaneously detect all the five polymorphisms based on multiplex PCR and minisequencing reaction. A total of 168 unrelated Chinese DNA samples were used to establish and evaluate the assay. Results: The different genotypes of the five polymorphisms could be determined by peak retention time and colors. DNA sequencing was performed on samples randomly selected from each of the genotype groups detected by SNaPshot assay, and the results indicated 100% concordance. Conclusion: The SNaPshot assay for the CYP3A5 and MDR1 five polymorphisms detection was accurate, automated, and cost-effective. (C) 2011 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
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页码:418 / 422
页数:5
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