Epigenetic modifications of DNA and RNA in Alzheimer's disease.

Alzheimer’s disease DNA methylation RNA modifications circRNAs epigenetics lncRNAs miRNAs non-coding RNAs

Journal

Frontiers in molecular neuroscience
ISSN: 1662-5099
Titre abrégé: Front Mol Neurosci
Pays: Switzerland
ID NLM: 101477914

Informations de publication

Date de publication:
2024
Historique:
received: 08 03 2024
accepted: 15 04 2024
medline: 10 5 2024
pubmed: 10 5 2024
entrez: 10 5 2024
Statut: epublish

Résumé

Alzheimer's disease (AD) is a complex neurodegenerative disorder and the most common form of dementia. There are two main types of AD: familial and sporadic. Familial AD is linked to mutations in amyloid precursor protein (APP), presenilin-1 (PSEN1), and presenilin-2 (PSEN2). On the other hand, sporadic AD is the more common form of the disease and has genetic, epigenetic, and environmental components that influence disease onset and progression. Investigating the epigenetic mechanisms associated with AD is essential for increasing understanding of pathology and identifying biomarkers for diagnosis and treatment. Chemical covalent modifications on DNA and RNA can epigenetically regulate gene expression at transcriptional and post-transcriptional levels and play protective or pathological roles in AD and other neurodegenerative diseases.

Identifiants

pubmed: 38726308
doi: 10.3389/fnmol.2024.1398026
pmc: PMC11079283
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1398026

Informations de copyright

Copyright © 2024 Martinez-Feduchi, Jin and Yao.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Paula Martinez-Feduchi (P)

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, United States.

Peng Jin (P)

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, United States.

Bing Yao (B)

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, United States.

Classifications MeSH