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Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans

Neurodegenerative diseases (NDs) such as Alzheimer’s disease (AD), Parkinson’s disease (PD), multiple sclerosis (MS), amyotrophic lateral sclerosis (ALS), and dementia pose one of the greatest health challenges this century. Although these NDs have been looked at as single entities, the underlying m...

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Autores principales: Brennan, Samuel, Keon, Matthew, Liu, Bing, Su, Zheng, Saksena, Nitin K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815273/
https://www.ncbi.nlm.nih.gov/pubmed/31037649
http://dx.doi.org/10.1007/s12035-019-1615-1
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author Brennan, Samuel
Keon, Matthew
Liu, Bing
Su, Zheng
Saksena, Nitin K.
author_facet Brennan, Samuel
Keon, Matthew
Liu, Bing
Su, Zheng
Saksena, Nitin K.
author_sort Brennan, Samuel
collection PubMed
description Neurodegenerative diseases (NDs) such as Alzheimer’s disease (AD), Parkinson’s disease (PD), multiple sclerosis (MS), amyotrophic lateral sclerosis (ALS), and dementia pose one of the greatest health challenges this century. Although these NDs have been looked at as single entities, the underlying molecular mechanisms have never been collectively visualized to date. With the advent of high-throughput genomic and proteomic technologies, we now have the opportunity to visualize these diseases in a whole new perspective, which will provide a clear understanding of the primary and secondary events vital in achieving the final resolution of these diseases guiding us to new treatment strategies to possibly treat these diseases together. We created a knowledge base of all microRNAs known to be differentially expressed in various body fluids of ND patients. We then used several bioinformatic methods to understand the functional intersections and differences between AD, PD, ALS, and MS. These results provide a unique panoramic view of possible functional intersections between AD, PD, MS, and ALS at the level of microRNA and their cognate genes and pathways, along with the entities that unify and separate them. While the microRNA signatures were apparent for each ND, the unique observation in our study was that hsa-miR-30b-5p overlapped between all four NDS, and has significant functional roles described across NDs. Furthermore, our results also show the evidence of functional convergence of miRNAs which was associated with the regulation of their cognate genes represented in pathways that included fatty acid synthesis and metabolism, ECM receptor interactions, prion diseases, and several signaling pathways critical to neuron differentiation and survival, underpinning their relevance in NDs. Envisioning this group of NDs together has allowed us to propose new ways of utilizing circulating miRNAs as biomarkers  and in visualizing diverse NDs more holistically . The critical molecular insights gained through the discovery of ND-associated miRNAs, overlapping miRNAs, and the functional convergence of microRNAs on vital pathways strongly implicated in neurodegenerative processes can prove immensely valuable in the identifying new generation of biomarkers, along with the development of miRNAs into therapeutics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-019-1615-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-68152732019-11-06 Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans Brennan, Samuel Keon, Matthew Liu, Bing Su, Zheng Saksena, Nitin K. Mol Neurobiol Article Neurodegenerative diseases (NDs) such as Alzheimer’s disease (AD), Parkinson’s disease (PD), multiple sclerosis (MS), amyotrophic lateral sclerosis (ALS), and dementia pose one of the greatest health challenges this century. Although these NDs have been looked at as single entities, the underlying molecular mechanisms have never been collectively visualized to date. With the advent of high-throughput genomic and proteomic technologies, we now have the opportunity to visualize these diseases in a whole new perspective, which will provide a clear understanding of the primary and secondary events vital in achieving the final resolution of these diseases guiding us to new treatment strategies to possibly treat these diseases together. We created a knowledge base of all microRNAs known to be differentially expressed in various body fluids of ND patients. We then used several bioinformatic methods to understand the functional intersections and differences between AD, PD, ALS, and MS. These results provide a unique panoramic view of possible functional intersections between AD, PD, MS, and ALS at the level of microRNA and their cognate genes and pathways, along with the entities that unify and separate them. While the microRNA signatures were apparent for each ND, the unique observation in our study was that hsa-miR-30b-5p overlapped between all four NDS, and has significant functional roles described across NDs. Furthermore, our results also show the evidence of functional convergence of miRNAs which was associated with the regulation of their cognate genes represented in pathways that included fatty acid synthesis and metabolism, ECM receptor interactions, prion diseases, and several signaling pathways critical to neuron differentiation and survival, underpinning their relevance in NDs. Envisioning this group of NDs together has allowed us to propose new ways of utilizing circulating miRNAs as biomarkers  and in visualizing diverse NDs more holistically . The critical molecular insights gained through the discovery of ND-associated miRNAs, overlapping miRNAs, and the functional convergence of microRNAs on vital pathways strongly implicated in neurodegenerative processes can prove immensely valuable in the identifying new generation of biomarkers, along with the development of miRNAs into therapeutics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-019-1615-1) contains supplementary material, which is available to authorized users. Springer US 2019-04-29 2019 /pmc/articles/PMC6815273/ /pubmed/31037649 http://dx.doi.org/10.1007/s12035-019-1615-1 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Brennan, Samuel
Keon, Matthew
Liu, Bing
Su, Zheng
Saksena, Nitin K.
Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans
title Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans
title_full Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans
title_fullStr Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans
title_full_unstemmed Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans
title_short Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans
title_sort panoramic visualization of circulating micrornas across neurodegenerative diseases in humans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815273/
https://www.ncbi.nlm.nih.gov/pubmed/31037649
http://dx.doi.org/10.1007/s12035-019-1615-1
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