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Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score

Idiopathic Pulmonary Fibrosis (IPF) is a rare disease of the respiratory system in which the lungs stiffen and get scarred, resulting in breathing weakness and eventually leading to death. Drug repurposing is a process that provides evidence for existing drugs that may also be effective in different...

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Autores principales: Karatzas, E., Bourdakou, M. M., Kolios, G., Spyrou, G. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626774/
https://www.ncbi.nlm.nih.gov/pubmed/28974751
http://dx.doi.org/10.1038/s41598-017-12849-8
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author Karatzas, E.
Bourdakou, M. M.
Kolios, G.
Spyrou, G. M.
author_facet Karatzas, E.
Bourdakou, M. M.
Kolios, G.
Spyrou, G. M.
author_sort Karatzas, E.
collection PubMed
description Idiopathic Pulmonary Fibrosis (IPF) is a rare disease of the respiratory system in which the lungs stiffen and get scarred, resulting in breathing weakness and eventually leading to death. Drug repurposing is a process that provides evidence for existing drugs that may also be effective in different diseases. In this study, we present a computational pipeline having as input a number of gene expression datasets from early and advanced stages of IPF and as output lists of repurposed drugs ranked with a novel composite score. We have devised and used a scoring formula in order to rank the repurposed drugs, consolidating the standard repurposing score with structural, functional and side effects’ scores for each drug per stage of IPF. The whole pipeline involves the selection of proper gene expression datasets, data preprocessing and statistical analysis, selection of the most important genes related to the disease, analysis of biological pathways, investigation of related molecular mechanisms, identification of fibrosis-related microRNAs, drug repurposing, structural and literature-based analysis of the repurposed drugs.
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spelling pubmed-56267742017-10-12 Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score Karatzas, E. Bourdakou, M. M. Kolios, G. Spyrou, G. M. Sci Rep Article Idiopathic Pulmonary Fibrosis (IPF) is a rare disease of the respiratory system in which the lungs stiffen and get scarred, resulting in breathing weakness and eventually leading to death. Drug repurposing is a process that provides evidence for existing drugs that may also be effective in different diseases. In this study, we present a computational pipeline having as input a number of gene expression datasets from early and advanced stages of IPF and as output lists of repurposed drugs ranked with a novel composite score. We have devised and used a scoring formula in order to rank the repurposed drugs, consolidating the standard repurposing score with structural, functional and side effects’ scores for each drug per stage of IPF. The whole pipeline involves the selection of proper gene expression datasets, data preprocessing and statistical analysis, selection of the most important genes related to the disease, analysis of biological pathways, investigation of related molecular mechanisms, identification of fibrosis-related microRNAs, drug repurposing, structural and literature-based analysis of the repurposed drugs. Nature Publishing Group UK 2017-10-03 /pmc/articles/PMC5626774/ /pubmed/28974751 http://dx.doi.org/10.1038/s41598-017-12849-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Karatzas, E.
Bourdakou, M. M.
Kolios, G.
Spyrou, G. M.
Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
title Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
title_full Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
title_fullStr Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
title_full_unstemmed Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
title_short Drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
title_sort drug repurposing in idiopathic pulmonary fibrosis filtered by a bioinformatics-derived composite score
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626774/
https://www.ncbi.nlm.nih.gov/pubmed/28974751
http://dx.doi.org/10.1038/s41598-017-12849-8
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