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Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)

Alzheimer’s disease (AD) and diabetes mellitus (DM) are known to have a shared molecular mechanism. We aimed to identify shared blood transcriptomic signatures between AD and DM. Blood expression datasets for each disease were combined and a co-expression network was used to construct modules consis...

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Detalles Bibliográficos
Autores principales: Lee, Taesic, Lee, Hyunju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823888/
https://www.ncbi.nlm.nih.gov/pubmed/33406707
http://dx.doi.org/10.3390/biomedicines9010034
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author Lee, Taesic
Lee, Hyunju
author_facet Lee, Taesic
Lee, Hyunju
author_sort Lee, Taesic
collection PubMed
description Alzheimer’s disease (AD) and diabetes mellitus (DM) are known to have a shared molecular mechanism. We aimed to identify shared blood transcriptomic signatures between AD and DM. Blood expression datasets for each disease were combined and a co-expression network was used to construct modules consisting of genes with similar expression patterns. For each module, a gene regulatory network based on gene expression and protein-protein interactions was established to identify hub genes. We selected one module, where COPS4, PSMA6, GTF2B, GTF2F2, and SSB were identified as dysregulated transcription factors that were common between AD and DM. These five genes were also differentially co-expressed in disease-related tissues, such as the brain in AD and the pancreas in DM. Our study identified gene modules that were dysregulated in both AD and DM blood samples, which may contribute to reveal common pathophysiology between two diseases.
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spelling pubmed-78238882021-01-24 Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†) Lee, Taesic Lee, Hyunju Biomedicines Article Alzheimer’s disease (AD) and diabetes mellitus (DM) are known to have a shared molecular mechanism. We aimed to identify shared blood transcriptomic signatures between AD and DM. Blood expression datasets for each disease were combined and a co-expression network was used to construct modules consisting of genes with similar expression patterns. For each module, a gene regulatory network based on gene expression and protein-protein interactions was established to identify hub genes. We selected one module, where COPS4, PSMA6, GTF2B, GTF2F2, and SSB were identified as dysregulated transcription factors that were common between AD and DM. These five genes were also differentially co-expressed in disease-related tissues, such as the brain in AD and the pancreas in DM. Our study identified gene modules that were dysregulated in both AD and DM blood samples, which may contribute to reveal common pathophysiology between two diseases. MDPI 2021-01-04 /pmc/articles/PMC7823888/ /pubmed/33406707 http://dx.doi.org/10.3390/biomedicines9010034 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Taesic
Lee, Hyunju
Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)
title Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)
title_full Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)
title_fullStr Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)
title_full_unstemmed Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)
title_short Shared Blood Transcriptomic Signatures between Alzheimer’s Disease and Diabetes Mellitus (†)
title_sort shared blood transcriptomic signatures between alzheimer’s disease and diabetes mellitus (†)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823888/
https://www.ncbi.nlm.nih.gov/pubmed/33406707
http://dx.doi.org/10.3390/biomedicines9010034
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