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Drug repurposing using meta-analysis of gene expression in Alzheimer’s disease

INTRODUCTION: Alzheimer’s disease and other forms of dementia are disease that bring an increased global burden. However, the medicine developed to date remains limited. The purpose of this study is to predict drug repositioning candidates using a computational method that integrates gene expression...

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Detalles Bibliográficos
Autores principales: Jang, Ha Young, Oh, Jung Mi, Kim, In-Wha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684643/
https://www.ncbi.nlm.nih.gov/pubmed/36440278
http://dx.doi.org/10.3389/fnins.2022.989174
Descripción
Sumario:INTRODUCTION: Alzheimer’s disease and other forms of dementia are disease that bring an increased global burden. However, the medicine developed to date remains limited. The purpose of this study is to predict drug repositioning candidates using a computational method that integrates gene expression profiles on Alzheimer’s disease and compound-induced changes in gene expression levels. METHODS: Gene expression data on Alzheimer’s disease were obtained from the Gene Expression Omnibus (GEO) and we conducted a meta-analysis of their gene expression levels. The reverse scores of compound-induced gene expressions were computed based on the reversal relationship between disease and drug gene expression profiles. RESULTS: Reversal genes and the candidate compounds were identified by the leave-one-out cross-validation procedure. Additionally, the half-maximal inhibitory concentration (IC50) values and the blood-brain barrier (BBB) permeability of candidate compounds were obtained from ChEMBL and PubChem, respectively. CONCLUSION: New therapeutic target genes and drug candidates against Alzheimer’s disease were identified by means of drug repositioning.