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Irinotecan pharmacokinetics/pharmacodynamics and UGT1A genetic polymorphisms in Japanese: roles of UGT1A1*6 and *28.伊立替康在日本人群中的药代动力学/药效学及UGT1A基因多态性:UGT1A1*6和*28的作用
Pharmacogenet Genomics. 2007 Jul;17(7):497-504. doi: 10.1097/FPC.0b013e328014341f.
2
Rapid detection of UGT1A1 gene polymorphisms by newly developed Invader assay.通过新开发的侵入法快速检测UGT1A1基因多态性。
Clin Chem. 2004 Aug;50(8):1479-80. doi: 10.1373/clinchem.2004.034694.
3
UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer.在接受伊立替康治疗的日本癌症患者中,UGT1A1单倍型与葡萄糖醛酸化减少及血清胆红素升高相关。
Clin Pharmacol Ther. 2004 Jun;75(6):501-15. doi: 10.1016/j.clpt.2004.01.010.
4
Comprehensive UGT1A1 genotyping in a Japanese population by pyrosequencing.
Clin Chem. 2003 Jul;49(7):1182-5. doi: 10.1373/49.7.1182.
5
Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38), an active metabolite of irinotecan (CPT-11), by human UGT1A1 variants, G71R, P229Q, and Y486D.人UGT1A1变体G71R、P229Q和Y486D对伊立替康(CPT-11)的活性代谢产物7-乙基-10-羟基喜树碱(SN-38)的葡萄糖醛酸化作用。
Drug Metab Dispos. 2003 Jan;31(1):108-13. doi: 10.1124/dmd.31.1.108.
6
Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER).通过结合改良引物延伸反应的生物发光测定法(BAMPER)对混合样本中的单核苷酸多态性进行定量检测。
Nucleic Acids Res. 2001 Oct 1;29(19):E93. doi: 10.1093/nar/29.19.e93.
7
High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers.采用通用能量转移标记引物通过等位基因特异性PCR进行高通量单核苷酸多态性基因分型。
Genome Res. 2001 Jan;11(1):163-9. doi: 10.1101/gr.157901.
8
Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays.使用通用高密度寡核苷酸标签阵列对人类单核苷酸多态性进行平行基因分型。
Genome Res. 2000 Jun;10(6):853-60. doi: 10.1101/gr.10.6.853.
9
Single-nucleotide polymorphism analysis by pyrosequencing.焦磷酸测序法进行单核苷酸多态性分析。
Anal Biochem. 2000 Apr 10;280(1):103-10. doi: 10.1006/abio.2000.4493.
10
The use of single-nucleotide polymorphism maps in pharmacogenomics.单核苷酸多态性图谱在药物基因组学中的应用。
Nat Biotechnol. 2000 May;18(5):505-8. doi: 10.1038/75360.

采用探针捕获与改良等位基因特异性引物延伸反应(MASPER)相结合的高通量单碱基错配检测法对 UDP-葡糖醛酸基转移酶 1A1(UGT1A1)进行基因分型。

High-throughput single-base mismatch detection for genotyping of UDP-glucuronosyltransferase (UGT1A1) with probe capture assay coupled with modified allele-specific primer extension reaction (MASPER).

机构信息

Japan Clinical Laboratories, Kumiyama, Kuze-gun, Kyoto, Japan.

出版信息

J Clin Lab Anal. 2010;24(2):85-91. doi: 10.1002/jcla.20359.

DOI:10.1002/jcla.20359
PMID:20333765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6647693/
Abstract

We have developed a new method based on specific primer extension reactions coupled with plate hybridization for high-throughput genotyping of single-base mutations. To improve the switching characteristics of the primer extension reaction, we introduced an artificial mismatch two bases upstream of the 3'-terminal base in the detection primers. A set of primers that correspond to wild-type and mutant DNA segments can be used to accurately analyze single-base mutations. The termini of these primers are at the mutation positions. The primer extension products produced by polymerase chain reaction (PCR) were captured by an oligonucleotide probe immobilized on the surface of microtiter wells and were detected by a colorimetric assay using the streptavidin-conjugated horseradish peroxidase. We used the new method to genotype 96 individuals for 211G>A (G71R) and 119 for 1456T>G (Y486D) in the UDP-glucuronosyltransferase1A1 gene; the results were completely concordant with those found by direct sequencing. The proposed method includes ordinary PCR and a microplate assay format, and may be used in routine laboratory tests.

摘要

我们开发了一种新的方法,基于特定引物延伸反应与平板杂交相结合,用于高通量单碱基突变的基因分型。为了改善引物延伸反应的切换特性,我们在检测引物的 3'-末端碱基上游引入了一个人工错配碱基对。一组与野生型和突变型 DNA 片段相对应的引物可用于准确分析单碱基突变。这些引物的末端位于突变位置。聚合酶链反应 (PCR) 产生的引物延伸产物被固定在微孔板表面的寡核苷酸探针捕获,并通过辣根过氧化物酶标记的链亲和素进行比色测定进行检测。我们使用新方法对 96 个人的 UDP-葡萄糖醛酸基转移酶 1A1 基因中的 211G>A (G71R) 和 119 个 1456T>G (Y486D) 进行了基因分型;结果与直接测序完全一致。所提出的方法包括普通 PCR 和微孔板检测方法,可用于常规实验室检测。