Aging Alters Hepatic DNA Hydroxymethylation, as Measured by Liquid Chromatography/Mass Spectrometry
Background:Aging is one of the most important risk factors for cancer. It appears that aberrant epigenetic changes might be a commondriver of aging and cancer. Among them are changes in DNA methylation and DNA hydroxymethylation. The 5’ carbon of cytosinesin CpG dinucleotides of DNA can be either me...
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Published in | Journal of cancer prevention pp. 301 - 308 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
대한암예방학회
01.12.2014
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Online Access | Get full text |
ISSN | 2288-3649 2288-3657 |
DOI | 10.15430/JCP.2014.19.2.301 |
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Abstract | Background:Aging is one of the most important risk factors for cancer. It appears that aberrant epigenetic changes might be a commondriver of aging and cancer. Among them are changes in DNA methylation and DNA hydroxymethylation. The 5’ carbon of cytosinesin CpG dinucleotides of DNA can be either methylated or hydroxymethylated. Like 5’-methylcytosine, changes in 5’-hydroxymethylcytosinemay occur due to aging, potentially leading to downstream changes in transcription and cancer development.
Methods:We set up a method to measure 5’-methyl-2’-deoxycytidine and 5’-hydroxymethyl-2’-deoxycytidine in DNA using liquidchromatography/mass spectrometry (LC/MS-MS) and used this method to measure the percentage of total cytosine that was eithermethylated or hydroxymethylated in the liver tissues of young and old C57Bl/6 male mice. The DNA was enzymatically hydrolyzed bysequential digestion with nuclease P1, phosphodiesterase I and alkaline phosphatase. The isotopomers [15N3]-2’-deoxycytidine and(methyl-d3, ring-6-d1)-5-methyl-2’-deoxycytidine were added to the DNA hydrolysates as internal standards. DNA methylation andhydroxymethylation were calculated as a percentage of total deoxycytidine in genomic DNA.
Results:Within day variations for DNA methylation and hydroxymethylation were 3.45% and 8.40%, while day to day variations were6.14% and 17.68%, respectively. Using this method it was determined that hepatic DNA of old mice had increased levels ofhydroxymethylation relative to young (0.32 ± 0.02% vs. 0.24 ± 0.01%, P= 0.02), with no significant changes in 5’-methylcytosine.
Conclusions:DNA hydroxymethylation measured by LC/MS-MS method can be a novel biomarker of aging. It will be useful to investigatethe potential role of DNA hydroxymethylation in the development and prevention of age-associated cancer. KCI Citation Count: 1 |
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AbstractList | Background:Aging is one of the most important risk factors for cancer. It appears that aberrant epigenetic changes might be a commondriver of aging and cancer. Among them are changes in DNA methylation and DNA hydroxymethylation. The 5’ carbon of cytosinesin CpG dinucleotides of DNA can be either methylated or hydroxymethylated. Like 5’-methylcytosine, changes in 5’-hydroxymethylcytosinemay occur due to aging, potentially leading to downstream changes in transcription and cancer development.
Methods:We set up a method to measure 5’-methyl-2’-deoxycytidine and 5’-hydroxymethyl-2’-deoxycytidine in DNA using liquidchromatography/mass spectrometry (LC/MS-MS) and used this method to measure the percentage of total cytosine that was eithermethylated or hydroxymethylated in the liver tissues of young and old C57Bl/6 male mice. The DNA was enzymatically hydrolyzed bysequential digestion with nuclease P1, phosphodiesterase I and alkaline phosphatase. The isotopomers [15N3]-2’-deoxycytidine and(methyl-d3, ring-6-d1)-5-methyl-2’-deoxycytidine were added to the DNA hydrolysates as internal standards. DNA methylation andhydroxymethylation were calculated as a percentage of total deoxycytidine in genomic DNA.
Results:Within day variations for DNA methylation and hydroxymethylation were 3.45% and 8.40%, while day to day variations were6.14% and 17.68%, respectively. Using this method it was determined that hepatic DNA of old mice had increased levels ofhydroxymethylation relative to young (0.32 ± 0.02% vs. 0.24 ± 0.01%, P= 0.02), with no significant changes in 5’-methylcytosine.
Conclusions:DNA hydroxymethylation measured by LC/MS-MS method can be a novel biomarker of aging. It will be useful to investigatethe potential role of DNA hydroxymethylation in the development and prevention of age-associated cancer. KCI Citation Count: 1 |
Author | 김경철 Lynne M. Ausman 최상운 Stephanie A. Tammen Zhenhua Liu Gregory G. Dolnikowski Simonetta Filippi |
Author_xml | – sequence: 1 fullname: Stephanie A. Tammen organization: (Tufts University) – sequence: 2 fullname: Gregory G. Dolnikowski organization: (Tufts University) – sequence: 3 fullname: Lynne M. Ausman organization: (Tufts University) – sequence: 4 fullname: Zhenhua Liu organization: (Tufts University) – sequence: 5 fullname: 김경철 organization: (차의과학대학교) – sequence: 6 fullname: Simonetta Filippi organization: (University of Verona) – sequence: 7 fullname: 최상운 organization: (차의과학대학교) |
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Snippet | Background:Aging is one of the most important risk factors for cancer. It appears that aberrant epigenetic changes might be a commondriver of aging and cancer.... |
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Title | Aging Alters Hepatic DNA Hydroxymethylation, as Measured by Liquid Chromatography/Mass Spectrometry |
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