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Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa
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 env...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572581/ https://www.ncbi.nlm.nih.gov/pubmed/23157586 http://dx.doi.org/10.1111/acel.12030 |
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author | Tapp, Henri S Commane, Daniel M Bradburn, D Michael Arasaradnam, Ramesh Mathers, John C Johnson, Ian T Belshaw, Nigel J |
author_facet | Tapp, Henri S Commane, Daniel M Bradburn, D Michael Arasaradnam, Ramesh Mathers, John C Johnson, Ian T Belshaw, Nigel J |
author_sort | Tapp, Henri S |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3572581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35725812013-02-14 Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa Tapp, Henri S Commane, Daniel M Bradburn, D Michael Arasaradnam, Ramesh Mathers, John C Johnson, Ian T Belshaw, Nigel J Aging Cell Original Articles 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. Blackwell Publishing Ltd 2013-02 2012-12-06 /pmc/articles/PMC3572581/ /pubmed/23157586 http://dx.doi.org/10.1111/acel.12030 Text en © 2013 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Tapp, Henri S Commane, Daniel M Bradburn, D Michael Arasaradnam, Ramesh Mathers, John C Johnson, Ian T Belshaw, Nigel J Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa |
title | Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa |
title_full | Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa |
title_fullStr | Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa |
title_full_unstemmed | Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa |
title_short | Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa |
title_sort | nutritional factors and gender influence age-related dna methylation in the human rectal mucosa |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572581/ https://www.ncbi.nlm.nih.gov/pubmed/23157586 http://dx.doi.org/10.1111/acel.12030 |
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