TY - JOUR
T1 - Methylation profiles of genes utilizing newly developed CpG island methylation microarray on colorectal cancer patients
AU - Kimura, Naoki
AU - Nagasaka, Takeshi
AU - Murakami, Jun
AU - Sasamoto, Hiromi
AU - Murakami, Masahiro
AU - Tanaka, Noriaki
AU - Matsubara, Nagahide
N1 - Funding Information:
We thank Natasha Koshnifsky for proof reading our manuscript. This study was partly supported by a Grant-in Aid from the Japanese Ministry of Education, Science, Sports and Culture of Japan (12671227, 11671237, 11671240, 14031227). Funding to pay the Open Access publication charges for this article was provided by Nisshinbo Industries Inc.
PY - 2005
Y1 - 2005
N2 - Aberrant methylation of DNA has been shown to play an important role in a variety of human cancers, developmental disorders and aging. Hence, aberrant methylation patterns in genes can be a molecular marker for such conditions. Therefore, a reliable but uncomplicated method to detect DNA methylation is preferred, not merely for research purposes but for daily clinical practice. To achieve these aims, we have established a precise system to identify DNA methylation patterns based on an oligonucleotide microarray technology. Our microarray method has an advantage over conventional methods and is unique because it allows the precise measurement of the methylation patterns within a target region. Our simple signal detection system depends on using an avidin-biotinylated peroxidase complex and does not require an expensive laser scanner or hazardous radioisotope. In this study, we applied our technique to detect promoter methylation status of O6-methylguanine-DNA methyltransferase (MGMT) gene. Our easy-handling technology provided reproducible and precise measurement of methylated CpGs in MGMT promoter and, thus, our method may bring about a potential evolution in the handling of a variety of high-throughput DNA methylation analyses for clinical purposes.
AB - Aberrant methylation of DNA has been shown to play an important role in a variety of human cancers, developmental disorders and aging. Hence, aberrant methylation patterns in genes can be a molecular marker for such conditions. Therefore, a reliable but uncomplicated method to detect DNA methylation is preferred, not merely for research purposes but for daily clinical practice. To achieve these aims, we have established a precise system to identify DNA methylation patterns based on an oligonucleotide microarray technology. Our microarray method has an advantage over conventional methods and is unique because it allows the precise measurement of the methylation patterns within a target region. Our simple signal detection system depends on using an avidin-biotinylated peroxidase complex and does not require an expensive laser scanner or hazardous radioisotope. In this study, we applied our technique to detect promoter methylation status of O6-methylguanine-DNA methyltransferase (MGMT) gene. Our easy-handling technology provided reproducible and precise measurement of methylated CpGs in MGMT promoter and, thus, our method may bring about a potential evolution in the handling of a variety of high-throughput DNA methylation analyses for clinical purposes.
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U2 - 10.1093/nar/gni046
DO - 10.1093/nar/gni046
M3 - Article
C2 - 15760842
AN - SCOPUS:26444610313
SN - 0305-1048
VL - 33
SP - 1
EP - 8
JO - Nucleic acids research
JF - Nucleic acids research
IS - 5
ER -