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 (AKAP12/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 (AKAP12/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. Copyright 2010 Elsevier B.V. All rights reserved.
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 (AKAP12/Gravin) promoter region and the accompanied underexpression of it has been noted in a variety of humancancers. METHODS: We applied methylation-specific high resolution melting (MS-HRM) technology to detect quantitatively A kinase anchor protein 12 (AKAP12/Gravin) methylation in peripheral blood from 100 colorectal cancerpatients 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. Copyright 2010 Elsevier B.V. All rights reserved.
Authors: M Naghitorabi; J Mohammadi Asl; H Mir Mohammad Sadeghi; M Rabbani; A Jafarian-Dehkordi; Haghjooye S Javanmard Journal: Res Pharm Sci Date: 2013-07
Authors: Mojgan Naghitorabi; Javad Mohammadi-Asl; Hamid Mir Mohammad Sadeghi; Mohammad Rabbani; Abbas Jafarian-Dehkordi; Shaghayegh Haghjooy Javanmard Journal: Adv Biomed Res Date: 2016-05-30
Authors: Yun-Fang Jia; YuBin Choi; Jennifer R Ayers-Ringler; Joanna M Biernacka; Jennifer R Geske; Daniel R Lindberg; Susan L McElroy; Mark A Frye; Doo-Sup Choi; Marin Veldic Journal: Front Cell Neurosci Date: 2017-07-21 Impact factor: 5.505
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