Rapid determination of AKAP12 promoter methylation levels in peripheral blood using methylation-sensitive high resolution melting (MS-HRM) analysis: Application in colorectal cancer

被引:23
|
作者
Liu, Weiwei [1 ]
Guan, Ming [1 ,2 ]
Su, Bing [3 ]
Li, Ji [4 ]
Ma, Weizhe
Liu, Chunfang [1 ]
Li, Min [1 ]
Lin, Yong [1 ]
Lu, Yuan [1 ]
机构
[1] Fudan Univ, Dept Lab Med, Huashan Hosp, Coll Med, Shanghai 200433, Peoples R China
[2] Fudan Univ, Cent Lab, Huashan Hosp, Shanghai 200433, Peoples R China
[3] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
[4] Fudan Univ, Dept Surg, Huashan Hosp, Shanghai 200433, Peoples R China
基金
上海市自然科学基金;
关键词
A kinase anchor protein 12; Methylation-sensitive high resolution melting (MS-HRM); Colorectal carcinoma; Peripheral blood; Circulating DNA; DNA METHYLATION; ABERRANT METHYLATION; BREAST-CANCER; HIGH-THROUGHPUT; CPG ISLAND; SERUM DNA; HYPERMETHYLATION; GENES; INACTIVATION; CADHERIN;
D O I
10.1016/j.cca.2010.03.003
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 Colorectal cancer is the third most common form of cancer and hypermethylation has been shown to increase the risk of developing this disease DNA hypermethylation in the A kinase anchor protein 12 (AKAPI2/Gravin) promoter region and the accompanied underexpression of it has been noted in a variety of human cancers Methods We applied methylation-specific high resolution melting (MS-HRM) technology to detect quantitatively A kinase anchor protein 12 (AKAPI2/Gravin) methylation in peripheral blood from 100 colorectal cancer patients and 50 healthy volunteers and in 3 colorectal cancer cell lines Results In this study 48 of the 100 colorectal cancer samples (48%) were found to be methylated at the AKAP12 promoter region AKAP12 methylation was significantly higher in the colorectal cancer samples with differentiation (p = 0 03) We also compared the results generated by MS-HRM with a traditional methylation-specific PCR (MSP) assay We found that intra-assay variability ranged from 6.14 to 9.90% and inter-assay variability ranged from 14.5 to 17.2% The AKAP12 MS-HRM assay was able to reproducibly detect 1% methylated DNA, whereas the MSP method was unable to detect less than 5% methylation Conclusions. We demonstrate the utility of quantitative AKAP12 MS-HRM analysis of promoter methylation in peripheral blood samples. AKAP12 MS-HRM quantitative methods with excellent detection capabilities have many promising applications in the research and diagnosis of colorectal cancer (C) 2010 Elsevier BV All rights reserved
引用
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页码:940 / 946
页数:7
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