A methylation sensitive dot blot assay (MS-DBA) for the quantitative analysis of DNA methylation in clinical samples

Details

Serval ID
serval:BIB_1848C26DE439
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A methylation sensitive dot blot assay (MS-DBA) for the quantitative analysis of DNA methylation in clinical samples
Journal
Journal of Clinical Pathology
Author(s)
Clement  G., Benhattar  J.
ISSN
0021-9746 (Print)
Publication state
Published
Issued date
2005
Volume
58
Number
2
Pages
155-158
Notes
PT - Journal Article PT - Research Support, Non-U.S. Gov't
Abstract
BACKGROUND: There is increasing interest in DNA methylation and in its implication in transcriptional gene silencing, a phenomenon commonly seen in human cancer. AIMS: To develop a new method that would allow quantitative DNA methylation analysis in a large range of clinical samples, independently of the processing protocol. METHODS: A methylation sensitive dot blot assay (MS-DBA) was developed, which is quantitative and combines bisulfite modification, PCR amplification using primers without CpG sites, and dot blot analysis with two probes specific for methylated and unmethylated DNA. RESULTS: The established method was used to study methylation of the hTERT, APC, and p16 promoter regions in microdissected, formalin fixed and paraffin wax embedded tissues. CONCLUSIONS: MS-DBA is a sensitive, specific, and quantitative approach to analyse DNA methylation in a variety of frozen or fixed tissues. Moreover, MS-DBA is rapid, easy to perform, and permits the screening of a large panel of samples in one experiment. Thus, MS-DBA can facilitate the routine analysis of DNA methylation in all types of clinical samples
Keywords
Adenocarcinoma/genetics/DNA Methylation/DNA Probes/DNA-Binding Proteins/Esophageal Neoplasms/Genes,p16/Humans/Immunoblotting/methods/Polymerase Chain Reaction/Promoter Regions (Genetics)/Telomerase/metabolism
Pubmed
Web of science
Open Access
Yes
Create date
29/01/2008 18:33
Last modification date
20/08/2019 12:48
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