Modification of allele-specific polymerase chain reaction for hMYH mutation analysis in Taiwanese patients with colorectal cancer

被引:2
|
作者
Gu, Yesong [1 ]
Fang, Ting-Ting [1 ]
Chao, Te-Hsin [2 ]
机构
[1] Tunghai Univ, Dept Chem & Mat Engn, Taichung 40704, Taiwan
[2] Taichung Vet Gen Hosp, Dept Surg, Taichung 40705, Taiwan
关键词
AS-PCR; hMYH; Mutations; Colorectal cancer; BASE EXCISION-REPAIR; HUMAN MUTY HOMOLOG; ADENOMATOUS POLYPOSIS; MYH GENE; PCR; INTERACTS; VARIANTS; MISMATCH;
D O I
10.1016/j.jtice.2010.11.002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
hMYH, a putative human E. coli MutY homology, can effectively remove adenine opposite to GO or G in duplex oligonucleotides with its glycosylase and AP lyase activities. Its germline mutations have been reported to be associated with colorectal cancer in Caucasian population. Plasmid DNA containing hMYH was employed to optimize the allele-specific polymerase chain reaction analysis conditions. The reliability of analysis was further improved by reducing the template concentration and adjusting annealing temperature. Genomic DNA of Taiwanese patients who had been diagnosed as colorectal cancer by the Taichung Veterans General Hospital were then examined for the mutations of hMYH, including G382D, Y165C and V232F. However, none of patients were detected with those reported mutations in hMYH. The relationship between the reported mutations of hMYH and colorectal cancer in Taiwan population is uncertain. Our results implicate that the frequencies of hMYH mutations may depend on the pathology of colorectal cancer and vary among different ethnic groups. (C) 2010 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:572 / 575
页数:4
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