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Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB

Age is well-known to be a significant factor in both disease pathology and response to treatment, yet the molecular changes that occur with age in humans remain ill-defined. Here, using transcriptome profiling of healthy human male skin, we demonstrate that there is a period of significantly elevate...

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Autores principales: Haustead, Daniel J., Stevenson, Andrew, Saxena, Vishal, Marriage, Fiona, Firth, Martin, Silla, Robyn, Martin, Lisa, Adcroft, Katharine F., Rea, Suzanne, Day, Philip J., Melton, Phillip, Wood, Fiona M., Fear, Mark W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882522/
https://www.ncbi.nlm.nih.gov/pubmed/27229172
http://dx.doi.org/10.1038/srep26846
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author Haustead, Daniel J.
Stevenson, Andrew
Saxena, Vishal
Marriage, Fiona
Firth, Martin
Silla, Robyn
Martin, Lisa
Adcroft, Katharine F.
Rea, Suzanne
Day, Philip J.
Melton, Phillip
Wood, Fiona M.
Fear, Mark W.
author_facet Haustead, Daniel J.
Stevenson, Andrew
Saxena, Vishal
Marriage, Fiona
Firth, Martin
Silla, Robyn
Martin, Lisa
Adcroft, Katharine F.
Rea, Suzanne
Day, Philip J.
Melton, Phillip
Wood, Fiona M.
Fear, Mark W.
author_sort Haustead, Daniel J.
collection PubMed
description Age is well-known to be a significant factor in both disease pathology and response to treatment, yet the molecular changes that occur with age in humans remain ill-defined. Here, using transcriptome profiling of healthy human male skin, we demonstrate that there is a period of significantly elevated, transcriptome-wide expression changes occurring predominantly in middle age. Both pre and post this period, the transcriptome appears to undergo much smaller, linear changes with increasing age. Functional analysis of the transient changes in middle age suggest a period of heightened metabolic activity and cellular damage associated with NF-kappa-B and TNF signaling pathways. Through meta-analysis we also show the presence of global, tissue independent linear transcriptome changes with age which appear to be regulated by NF-kappa-B. These results suggest that aging in human skin is associated with a critical mid-life period with widespread transcriptome changes, both preceded and proceeded by a relatively steady rate of linear change in the transcriptome. The data provides insight into molecular changes associated with normal aging and will help to better understand the increasingly important pathological changes associated with aging.
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spelling pubmed-48825222016-06-08 Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB Haustead, Daniel J. Stevenson, Andrew Saxena, Vishal Marriage, Fiona Firth, Martin Silla, Robyn Martin, Lisa Adcroft, Katharine F. Rea, Suzanne Day, Philip J. Melton, Phillip Wood, Fiona M. Fear, Mark W. Sci Rep Article Age is well-known to be a significant factor in both disease pathology and response to treatment, yet the molecular changes that occur with age in humans remain ill-defined. Here, using transcriptome profiling of healthy human male skin, we demonstrate that there is a period of significantly elevated, transcriptome-wide expression changes occurring predominantly in middle age. Both pre and post this period, the transcriptome appears to undergo much smaller, linear changes with increasing age. Functional analysis of the transient changes in middle age suggest a period of heightened metabolic activity and cellular damage associated with NF-kappa-B and TNF signaling pathways. Through meta-analysis we also show the presence of global, tissue independent linear transcriptome changes with age which appear to be regulated by NF-kappa-B. These results suggest that aging in human skin is associated with a critical mid-life period with widespread transcriptome changes, both preceded and proceeded by a relatively steady rate of linear change in the transcriptome. The data provides insight into molecular changes associated with normal aging and will help to better understand the increasingly important pathological changes associated with aging. Nature Publishing Group 2016-05-27 /pmc/articles/PMC4882522/ /pubmed/27229172 http://dx.doi.org/10.1038/srep26846 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Haustead, Daniel J.
Stevenson, Andrew
Saxena, Vishal
Marriage, Fiona
Firth, Martin
Silla, Robyn
Martin, Lisa
Adcroft, Katharine F.
Rea, Suzanne
Day, Philip J.
Melton, Phillip
Wood, Fiona M.
Fear, Mark W.
Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB
title Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB
title_full Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB
title_fullStr Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB
title_full_unstemmed Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB
title_short Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB
title_sort transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of nf-κb
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882522/
https://www.ncbi.nlm.nih.gov/pubmed/27229172
http://dx.doi.org/10.1038/srep26846
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