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MicroRNA Networks in Cognition and Dementia

The change from viewing noncoding RNA as “junk” in the genome to seeing it as a critical epigenetic regulator in almost every human condition or disease has forced a paradigm shift in biomedical and clinical research. Small and long noncoding RNA transcripts are now routinely evaluated as putative d...

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Detalles Bibliográficos
Autores principales: Blount, Grace S., Coursey, Layton, Kocerha, Jannet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221254/
https://www.ncbi.nlm.nih.gov/pubmed/35741010
http://dx.doi.org/10.3390/cells11121882
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author Blount, Grace S.
Coursey, Layton
Kocerha, Jannet
author_facet Blount, Grace S.
Coursey, Layton
Kocerha, Jannet
author_sort Blount, Grace S.
collection PubMed
description The change from viewing noncoding RNA as “junk” in the genome to seeing it as a critical epigenetic regulator in almost every human condition or disease has forced a paradigm shift in biomedical and clinical research. Small and long noncoding RNA transcripts are now routinely evaluated as putative diagnostic or therapeutic agents. A prominent role for noncoding microRNAs in the central nervous system has uncovered promising new clinical candidates for dementia-related disorders, treatments for which currently remain elusive even as the percentage of diagnosed patients increases significantly. Cognitive decline is a core neurodegenerative process in Alzheimer’s Disease, Frontotemporal Dementia, Lewy body dementia, vascular dementia, Huntington’s Disease, Creutzfeldt–Jakob disease, and a significant portion of Parkinson’s Disease patients. This review will discuss the microRNA-associated networks which influence these pathologies, including inflammatory and viral-mediated pathways (such as the novel SARS-CoV-2 virus implicated in COVID-19), and their current status in clinical trials.
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spelling pubmed-92212542022-06-24 MicroRNA Networks in Cognition and Dementia Blount, Grace S. Coursey, Layton Kocerha, Jannet Cells Review The change from viewing noncoding RNA as “junk” in the genome to seeing it as a critical epigenetic regulator in almost every human condition or disease has forced a paradigm shift in biomedical and clinical research. Small and long noncoding RNA transcripts are now routinely evaluated as putative diagnostic or therapeutic agents. A prominent role for noncoding microRNAs in the central nervous system has uncovered promising new clinical candidates for dementia-related disorders, treatments for which currently remain elusive even as the percentage of diagnosed patients increases significantly. Cognitive decline is a core neurodegenerative process in Alzheimer’s Disease, Frontotemporal Dementia, Lewy body dementia, vascular dementia, Huntington’s Disease, Creutzfeldt–Jakob disease, and a significant portion of Parkinson’s Disease patients. This review will discuss the microRNA-associated networks which influence these pathologies, including inflammatory and viral-mediated pathways (such as the novel SARS-CoV-2 virus implicated in COVID-19), and their current status in clinical trials. MDPI 2022-06-09 /pmc/articles/PMC9221254/ /pubmed/35741010 http://dx.doi.org/10.3390/cells11121882 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Blount, Grace S.
Coursey, Layton
Kocerha, Jannet
MicroRNA Networks in Cognition and Dementia
title MicroRNA Networks in Cognition and Dementia
title_full MicroRNA Networks in Cognition and Dementia
title_fullStr MicroRNA Networks in Cognition and Dementia
title_full_unstemmed MicroRNA Networks in Cognition and Dementia
title_short MicroRNA Networks in Cognition and Dementia
title_sort microrna networks in cognition and dementia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221254/
https://www.ncbi.nlm.nih.gov/pubmed/35741010
http://dx.doi.org/10.3390/cells11121882
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