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The histone code in dementia: Transcriptional and chromatin plasticity fades away

With the aging of the population, Alzheimer's disease and other forms of dementia represent major challenges for health care systems globally. To date, the molecular mechanisms underlying the pathophysiology of dementia remain elusive, with a consequent negative impact in developing efficient d...

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Detalles Bibliográficos
Autores principales: Bano, Daniele, Salomoni, Paolo, Ehninger, Dan, Nicotera, Pierluigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519393/
https://www.ncbi.nlm.nih.gov/pubmed/34411982
http://dx.doi.org/10.1016/j.coph.2021.07.014
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author Bano, Daniele
Salomoni, Paolo
Ehninger, Dan
Nicotera, Pierluigi
author_facet Bano, Daniele
Salomoni, Paolo
Ehninger, Dan
Nicotera, Pierluigi
author_sort Bano, Daniele
collection PubMed
description With the aging of the population, Alzheimer's disease and other forms of dementia represent major challenges for health care systems globally. To date, the molecular mechanisms underlying the pathophysiology of dementia remain elusive, with a consequent negative impact in developing efficient disease modifiers. New exciting findings suggest that modulation of the histone code may influence transcriptional networks at the root of neuronal plasticity and cognitive performance. Although most of the current conclusions require further mechanistic evidence, it appears that chromatin perturbations actually correlate with Alzheimer's disease onset and progression. Thus, a better understanding of the epigenetic contribution to normal brain function and dementia pathogenesis may help to identify new epigenetic targets for the inhibition of disease trajectories associated with cognitive decline.
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spelling pubmed-85193932021-10-21 The histone code in dementia: Transcriptional and chromatin plasticity fades away Bano, Daniele Salomoni, Paolo Ehninger, Dan Nicotera, Pierluigi Curr Opin Pharmacol Article With the aging of the population, Alzheimer's disease and other forms of dementia represent major challenges for health care systems globally. To date, the molecular mechanisms underlying the pathophysiology of dementia remain elusive, with a consequent negative impact in developing efficient disease modifiers. New exciting findings suggest that modulation of the histone code may influence transcriptional networks at the root of neuronal plasticity and cognitive performance. Although most of the current conclusions require further mechanistic evidence, it appears that chromatin perturbations actually correlate with Alzheimer's disease onset and progression. Thus, a better understanding of the epigenetic contribution to normal brain function and dementia pathogenesis may help to identify new epigenetic targets for the inhibition of disease trajectories associated with cognitive decline. Elsevier Science Ltd 2021-10 /pmc/articles/PMC8519393/ /pubmed/34411982 http://dx.doi.org/10.1016/j.coph.2021.07.014 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bano, Daniele
Salomoni, Paolo
Ehninger, Dan
Nicotera, Pierluigi
The histone code in dementia: Transcriptional and chromatin plasticity fades away
title The histone code in dementia: Transcriptional and chromatin plasticity fades away
title_full The histone code in dementia: Transcriptional and chromatin plasticity fades away
title_fullStr The histone code in dementia: Transcriptional and chromatin plasticity fades away
title_full_unstemmed The histone code in dementia: Transcriptional and chromatin plasticity fades away
title_short The histone code in dementia: Transcriptional and chromatin plasticity fades away
title_sort histone code in dementia: transcriptional and chromatin plasticity fades away
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519393/
https://www.ncbi.nlm.nih.gov/pubmed/34411982
http://dx.doi.org/10.1016/j.coph.2021.07.014
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