Epigenetic mechanisms during ageing and neurogenesis as novel therapeutic avenues in human brain disorders

dc.contributor.authorDelgado Morales, Raul
dc.contributor.authorAgís Balboa, Roberto Carlos
dc.contributor.authorEsteller, Manel, 1968-
dc.contributor.authorBerdasco, María
dc.date.accessioned2019-01-15T08:54:36Z
dc.date.available2019-01-15T08:54:36Z
dc.date.issued2017-06-29
dc.date.updated2019-01-15T08:54:36Z
dc.description.abstractAgeing is the main risk factor for human neurological disorders. Among the diverse molecular pathways that govern ageing, epigenetics can guide age-associated decline in part by regulating gene expression and also through the modulation of genomic instability and high-order chromatin architecture. Epigenetic mechanisms are involved in the regulation of neural differentiation as well as in functional processes related to memory consolidation, learning or cognition during healthy lifespan. On the other side of the coin, many neurodegenerative diseases are associated with epigenetic dysregulation. The reversible nature of epigenetic factors and, especially, their role as mediators between the genome and the environment make them exciting candidates as therapeutic targets. Rather than providing a broad description of the pathways epigenetically deregulated in human neurological disorders, in this review, we have focused on the potential use of epigenetic enzymes as druggable targets to ameliorate neural decline during normal ageing and especially in neurological disorders. We will firstly discuss recent progress that supports a key role of epigenetic regulation during healthy ageing with an emphasis on the role of epigenetic regulation in adult neurogenesis. Then, we will focus on epigenetic alterations associated with ageing-related human disorders of the central nervous system. We will discuss examples in the context of psychiatric disorders, including schizophrenia and posttraumatic stress disorders, and also dementia or Alzheimer's disease as the most frequent neurodegenerative disease. Finally, methodological limitations and future perspectives are discussed.
dc.format.extent18 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec677356
dc.identifier.issn1868-7075
dc.identifier.pmid28670349
dc.identifier.urihttps://hdl.handle.net/2445/127256
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1186/s13148-017-0365-z
dc.relation.ispartofClinical Epigenetics, 2017, vol. 9, p. 67
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/643417/EU//JPco-fuND
dc.relation.urihttps://doi.org/10.1186/s13148-017-0365-z
dc.rightscc-by (c) Delgado Morales, Raúl et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Ciències Fisiològiques)
dc.subject.classificationEpigenètica
dc.subject.classificationADN
dc.subject.classificationMetilació
dc.subject.classificationNeurobiologia del desenvolupament
dc.subject.classificationEnvelliment cerebral
dc.subject.classificationNeurones
dc.subject.classificationCervell
dc.subject.otherEpigenetics
dc.subject.otherDNA
dc.subject.otherMethylation
dc.subject.otherDevelopmental neurobiology
dc.subject.otherAging brain
dc.subject.otherNeurons
dc.subject.otherBrain
dc.titleEpigenetic mechanisms during ageing and neurogenesis as novel therapeutic avenues in human brain disorders
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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