Nutritional factors and gender influence age‐related DNA methylation in the human rectal mucosa
Summary Aberrant methylation of CpG islands (CGI) occurs in many genes expressed in colonic epithelial cells, and may contribute to the dysregulation of signalling pathways associated with carcinogenesis. This cross‐sectional study assessed the relative importance of age, nutritional exposures and o...
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Veröffentlicht in: | Aging cell 2013-02, Vol.12 (1), p.148-155 |
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description | Summary
Aberrant methylation of CpG islands (CGI) occurs in many genes expressed in colonic epithelial cells, and may contribute to the dysregulation of signalling pathways associated with carcinogenesis. This cross‐sectional study assessed the relative importance of age, nutritional exposures and other environmental factors in the development of CGI methylation. Rectal biopsies were obtained from 185 individuals (84 male, 101 female) shown to be free of colorectal disease, and for whom measurements of age, body size, nutritional status and blood cell counts were available. We used quantitative DNA methylation analysis combined with multivariate modelling to investigate the relationships between nutritional, anthropometric and metabolic factors and the CGI methylation of 11 genes, together with LINE‐1 as an index of global DNA methylation. Age was a consistent predictor of CGI methylation for 9/11 genes but significant positive associations with folate status and negative associations with vitamin D and selenium status were also identified for several genes. There was evidence for positive associations with blood monocyte levels and anthropometric factors for some genes. In general, CGI methylation was higher in males than in females and differential effects of age and other factors on methylation in males and females were identified. In conclusion, levels of age‐related CGI methylation in the healthy human rectal mucosa are influenced by gender, the availability of folate, vitamin D and selenium, and perhaps by factors related to systemic inflammation. |
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Aberrant methylation of CpG islands (CGI) occurs in many genes expressed in colonic epithelial cells, and may contribute to the dysregulation of signalling pathways associated with carcinogenesis. This cross‐sectional study assessed the relative importance of age, nutritional exposures and other environmental factors in the development of CGI methylation. Rectal biopsies were obtained from 185 individuals (84 male, 101 female) shown to be free of colorectal disease, and for whom measurements of age, body size, nutritional status and blood cell counts were available. We used quantitative DNA methylation analysis combined with multivariate modelling to investigate the relationships between nutritional, anthropometric and metabolic factors and the CGI methylation of 11 genes, together with LINE‐1 as an index of global DNA methylation. Age was a consistent predictor of CGI methylation for 9/11 genes but significant positive associations with folate status and negative associations with vitamin D and selenium status were also identified for several genes. There was evidence for positive associations with blood monocyte levels and anthropometric factors for some genes. In general, CGI methylation was higher in males than in females and differential effects of age and other factors on methylation in males and females were identified. In conclusion, levels of age‐related CGI methylation in the healthy human rectal mucosa are influenced by gender, the availability of folate, vitamin D and selenium, and perhaps by factors related to systemic inflammation.</description><identifier>ISSN: 1474-9718</identifier><identifier>EISSN: 1474-9726</identifier><identifier>DOI: 10.1111/acel.12030</identifier><identifier>PMID: 23157586</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adolescent ; Adult ; Age ; Age Factors ; Aged ; aging ; colorectal cancer ; CpG Islands ; Deoxyribonucleic acid ; DNA ; DNA Methylation ; Feeding Behavior ; Female ; folate ; Folic Acid - blood ; Folic Acid - metabolism ; Humans ; Intestinal Mucosa - metabolism ; Intestinal Mucosa - pathology ; Intestinal Mucosa - physiology ; Leukocyte Count ; Male ; Middle Aged ; nutrition ; Original ; Rectum - metabolism ; Rectum - pathology ; Rectum - physiology ; Sex Factors ; Studies ; Young Adult</subject><ispartof>Aging cell, 2013-02, Vol.12 (1), p.148-155</ispartof><rights>2012 The Authors Aging Cell © 2012 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland</rights><rights>2012 The Authors Aging Cell © 2012 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland.</rights><rights>2013 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland</rights><rights>2013 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4890-6da3c24ae2e2576202c2c28b5707c427a9ef77d340bb7d906f6d665af83f99ce3</citedby><cites>FETCH-LOGICAL-c4890-6da3c24ae2e2576202c2c28b5707c427a9ef77d340bb7d906f6d665af83f99ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572581/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572581/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23157586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tapp, Henri S.</creatorcontrib><creatorcontrib>Commane, Daniel M.</creatorcontrib><creatorcontrib>Bradburn, D. Michael</creatorcontrib><creatorcontrib>Arasaradnam, Ramesh</creatorcontrib><creatorcontrib>Mathers, John C.</creatorcontrib><creatorcontrib>Johnson, Ian T.</creatorcontrib><creatorcontrib>Belshaw, Nigel J.</creatorcontrib><title>Nutritional factors and gender influence age‐related DNA methylation in the human rectal mucosa</title><title>Aging cell</title><addtitle>Aging Cell</addtitle><description>Summary
Aberrant methylation of CpG islands (CGI) occurs in many genes expressed in colonic epithelial cells, and may contribute to the dysregulation of signalling pathways associated with carcinogenesis. This cross‐sectional study assessed the relative importance of age, nutritional exposures and other environmental factors in the development of CGI methylation. Rectal biopsies were obtained from 185 individuals (84 male, 101 female) shown to be free of colorectal disease, and for whom measurements of age, body size, nutritional status and blood cell counts were available. We used quantitative DNA methylation analysis combined with multivariate modelling to investigate the relationships between nutritional, anthropometric and metabolic factors and the CGI methylation of 11 genes, together with LINE‐1 as an index of global DNA methylation. Age was a consistent predictor of CGI methylation for 9/11 genes but significant positive associations with folate status and negative associations with vitamin D and selenium status were also identified for several genes. There was evidence for positive associations with blood monocyte levels and anthropometric factors for some genes. In general, CGI methylation was higher in males than in females and differential effects of age and other factors on methylation in males and females were identified. In conclusion, levels of age‐related CGI methylation in the healthy human rectal mucosa are influenced by gender, the availability of folate, vitamin D and selenium, and perhaps by factors related to systemic inflammation.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Age Factors</subject><subject>Aged</subject><subject>aging</subject><subject>colorectal cancer</subject><subject>CpG Islands</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Methylation</subject><subject>Feeding Behavior</subject><subject>Female</subject><subject>folate</subject><subject>Folic Acid - blood</subject><subject>Folic Acid - metabolism</subject><subject>Humans</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestinal Mucosa - pathology</subject><subject>Intestinal Mucosa - physiology</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Middle Aged</subject><subject>nutrition</subject><subject>Original</subject><subject>Rectum - metabolism</subject><subject>Rectum - pathology</subject><subject>Rectum - physiology</subject><subject>Sex Factors</subject><subject>Studies</subject><subject>Young Adult</subject><issn>1474-9718</issn><issn>1474-9726</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp9kctOAyEUhonRaL1sfABD4s6kFZgZmNmYNLVekkY3uianzJl2zFwqMJrufASf0SeRWm10IyyA8PFxcn5Cjjkb8DDOwWA14IJFbIv0eKzifqaE3N7sebpH9p17YoyrjEW7ZE9EPFFJKnsE7jpvS1-2DVS0AONb6yg0OZ1hk6OlZVNUHTYGKczw4-3dYgUec3p5N6Q1-vkyHMPjwFE_RzrvamioReODru5M6-CQ7BRQOTz6Xg_I49X4YXTTn9xf346Gk76J04z1ZQ6RETGgQJEoKZgwYabTRDFlYqEgw0KpPIrZdKryjMlC5lImUKRRkWUGowNysfYuummNucHGW6j0wpY12KVuodR_b5pyrmfti44SJZKUB8Hpt8C2zx06r5_azoa-OM2FYnGoKZWBOltTxrbOWSw2P3CmV3HoVRz6K44An_yuaYP-9D8AfA28lhUu_1Hp4Wg8WUs_AbR3l4g</recordid><startdate>201302</startdate><enddate>201302</enddate><creator>Tapp, Henri S.</creator><creator>Commane, Daniel M.</creator><creator>Bradburn, D. Michael</creator><creator>Arasaradnam, Ramesh</creator><creator>Mathers, John C.</creator><creator>Johnson, Ian T.</creator><creator>Belshaw, Nigel J.</creator><general>John Wiley & Sons, Inc</general><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>201302</creationdate><title>Nutritional factors and gender influence age‐related DNA methylation in the human rectal mucosa</title><author>Tapp, Henri S. ; Commane, Daniel M. ; Bradburn, D. Michael ; Arasaradnam, Ramesh ; Mathers, John C. ; Johnson, Ian T. ; Belshaw, Nigel J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4890-6da3c24ae2e2576202c2c28b5707c427a9ef77d340bb7d906f6d665af83f99ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age</topic><topic>Age Factors</topic><topic>Aged</topic><topic>aging</topic><topic>colorectal cancer</topic><topic>CpG Islands</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Methylation</topic><topic>Feeding Behavior</topic><topic>Female</topic><topic>folate</topic><topic>Folic Acid - blood</topic><topic>Folic Acid - metabolism</topic><topic>Humans</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestinal Mucosa - pathology</topic><topic>Intestinal Mucosa - physiology</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Middle Aged</topic><topic>nutrition</topic><topic>Original</topic><topic>Rectum - metabolism</topic><topic>Rectum - pathology</topic><topic>Rectum - physiology</topic><topic>Sex Factors</topic><topic>Studies</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tapp, Henri S.</creatorcontrib><creatorcontrib>Commane, Daniel M.</creatorcontrib><creatorcontrib>Bradburn, D. Michael</creatorcontrib><creatorcontrib>Arasaradnam, Ramesh</creatorcontrib><creatorcontrib>Mathers, John C.</creatorcontrib><creatorcontrib>Johnson, Ian T.</creatorcontrib><creatorcontrib>Belshaw, Nigel J.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Aging cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tapp, Henri S.</au><au>Commane, Daniel M.</au><au>Bradburn, D. Michael</au><au>Arasaradnam, Ramesh</au><au>Mathers, John C.</au><au>Johnson, Ian T.</au><au>Belshaw, Nigel J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nutritional factors and gender influence age‐related DNA methylation in the human rectal mucosa</atitle><jtitle>Aging cell</jtitle><addtitle>Aging Cell</addtitle><date>2013-02</date><risdate>2013</risdate><volume>12</volume><issue>1</issue><spage>148</spage><epage>155</epage><pages>148-155</pages><issn>1474-9718</issn><eissn>1474-9726</eissn><abstract>Summary
Aberrant methylation of CpG islands (CGI) occurs in many genes expressed in colonic epithelial cells, and may contribute to the dysregulation of signalling pathways associated with carcinogenesis. This cross‐sectional study assessed the relative importance of age, nutritional exposures and other environmental factors in the development of CGI methylation. Rectal biopsies were obtained from 185 individuals (84 male, 101 female) shown to be free of colorectal disease, and for whom measurements of age, body size, nutritional status and blood cell counts were available. We used quantitative DNA methylation analysis combined with multivariate modelling to investigate the relationships between nutritional, anthropometric and metabolic factors and the CGI methylation of 11 genes, together with LINE‐1 as an index of global DNA methylation. Age was a consistent predictor of CGI methylation for 9/11 genes but significant positive associations with folate status and negative associations with vitamin D and selenium status were also identified for several genes. There was evidence for positive associations with blood monocyte levels and anthropometric factors for some genes. In general, CGI methylation was higher in males than in females and differential effects of age and other factors on methylation in males and females were identified. In conclusion, levels of age‐related CGI methylation in the healthy human rectal mucosa are influenced by gender, the availability of folate, vitamin D and selenium, and perhaps by factors related to systemic inflammation.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>23157586</pmid><doi>10.1111/acel.12030</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age Age Factors Aged aging colorectal cancer CpG Islands Deoxyribonucleic acid DNA DNA Methylation Feeding Behavior Female folate Folic Acid - blood Folic Acid - metabolism Humans Intestinal Mucosa - metabolism Intestinal Mucosa - pathology Intestinal Mucosa - physiology Leukocyte Count Male Middle Aged nutrition Original Rectum - metabolism Rectum - pathology Rectum - physiology Sex Factors Studies Young Adult |
title | Nutritional factors and gender influence age‐related DNA methylation in the human rectal mucosa |
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