A novel method for sensitive and specific detection of DNA methylation biomarkers based on DNA restriction during PCR cycling

DNA methylation is an important epigenetic mechanism involved in fundamental biological processes such as development, imprinting, and carcino-genesis. For these reasons, DNA methylation represents a valuable source for cancer biomarkers. Methods for the sensitive and specific detection of methylate...

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Veröffentlicht in:BioTechniques. - 1993. - 47(2009), 3 vom: 23. Sept., Seite 737-44
1. Verfasser: Kneip, Christoph (VerfasserIn)
Weitere Verfasser: Schmidt, Bernd, Fleischhacker, Michael, Seegebarth, Anke, Lewin, Jörn, Flemming, Nadja, Seemann, Stefanie, Schlegel, Thomas, Witt, Christian, Liebenberg, Volker, Dietrich, Dimo
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Evaluation Study Journal Article BARHL2 protein, human Biomarkers, Tumor DNA, Neoplasm Homeodomain Proteins Nerve Tissue Proteins DNA Restriction Enzymes EC 3.1.21.-
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245 1 2 |a A novel method for sensitive and specific detection of DNA methylation biomarkers based on DNA restriction during PCR cycling 
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520 |a DNA methylation is an important epigenetic mechanism involved in fundamental biological processes such as development, imprinting, and carcino-genesis. For these reasons, DNA methylation represents a valuable source for cancer biomarkers. Methods for the sensitive and specific detection of methylated DNA are a prerequisite for the implementation of DNA biomarkers into clinical routine when early detection based on the analysis of body fluids is desired. Here, a novel technique is presented for the detection of DNA methylation biomarkers, based on real-time PCR of bisulfite-treated template with enzymatic digestion of background DNA during amplification using the heat-stable enzyme Tsp509I. An assay for the lung cancer methylation biomarker BARHL2 was used to show clinical and analytical performance of the method in comparison with methylation-specific PCR technology. Both technologies showed comparable performance when analyzing technical DNA mixtures and bronchial lavage samples from 75 patients suspected of having lung cancer. The results demonstrate that the approach is useful for sensitive and specific detection of a few copies of methylated DNA in samples with a high background of unmethylated DNA, such as in clinical samples from body fluids 
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650 7 |a EC 3.1.21.-  |2 NLM 
700 1 |a Schmidt, Bernd  |e verfasserin  |4 aut 
700 1 |a Fleischhacker, Michael  |e verfasserin  |4 aut 
700 1 |a Seegebarth, Anke  |e verfasserin  |4 aut 
700 1 |a Lewin, Jörn  |e verfasserin  |4 aut 
700 1 |a Flemming, Nadja  |e verfasserin  |4 aut 
700 1 |a Seemann, Stefanie  |e verfasserin  |4 aut 
700 1 |a Schlegel, Thomas  |e verfasserin  |4 aut 
700 1 |a Witt, Christian  |e verfasserin  |4 aut 
700 1 |a Liebenberg, Volker  |e verfasserin  |4 aut 
700 1 |a Dietrich, Dimo  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t BioTechniques  |d 1993  |g 47(2009), 3 vom: 23. Sept., Seite 737-44  |w (DE-627)NLM012627046  |x 1940-9818  |7 nnns 
773 1 8 |g volume:47  |g year:2009  |g number:3  |g day:23  |g month:09  |g pages:737-44 
856 4 0 |u http://dx.doi.org/10.2144/000113208  |3 Volltext 
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