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The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases
A gene expression signature (GES) is a group of genes that shows a unique expression profile as a result of perturbations by drugs, genetic modification or diseases on the transcriptional machinery. The comparisons between GES profiles have been used to investigate the relationships between drugs, t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357095/ https://www.ncbi.nlm.nih.gov/pubmed/32560162 http://dx.doi.org/10.3390/molecules25122776 |
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author | Qi, Xiguang Shen, Mingzhe Fan, Peihao Guo, Xiaojiang Wang, Tianqi Feng, Ning Zhang, Manling Sweet, Robert A. Kirisci, Levent Wang, Lirong |
author_facet | Qi, Xiguang Shen, Mingzhe Fan, Peihao Guo, Xiaojiang Wang, Tianqi Feng, Ning Zhang, Manling Sweet, Robert A. Kirisci, Levent Wang, Lirong |
author_sort | Qi, Xiguang |
collection | PubMed |
description | A gene expression signature (GES) is a group of genes that shows a unique expression profile as a result of perturbations by drugs, genetic modification or diseases on the transcriptional machinery. The comparisons between GES profiles have been used to investigate the relationships between drugs, their targets and diseases with quite a few successful cases reported. Especially in the study of GES-guided drugs–disease associations, researchers believe that if a GES induced by a drug is opposite to a GES induced by a disease, the drug may have potential as a treatment of that disease. In this study, we data-mined the crowd extracted expression of differential signatures (CREEDS) database to evaluate the similarity between GES profiles from drugs and their indicated diseases. Our study aims to explore the application domains of GES-guided drug–disease associations through the analysis of the similarity of GES profiles on known pairs of drug–disease associations, thereby identifying subgroups of drugs/diseases that are suitable for GES-guided drug repositioning approaches. Our results supported our hypothesis that the GES-guided drug–disease association method is better suited for some subgroups or pathways such as drugs and diseases associated with the immune system, diseases of the nervous system, non-chemotherapy drugs or the mTOR signaling pathway. |
format | Online Article Text |
id | pubmed-7357095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73570952020-07-23 The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases Qi, Xiguang Shen, Mingzhe Fan, Peihao Guo, Xiaojiang Wang, Tianqi Feng, Ning Zhang, Manling Sweet, Robert A. Kirisci, Levent Wang, Lirong Molecules Article A gene expression signature (GES) is a group of genes that shows a unique expression profile as a result of perturbations by drugs, genetic modification or diseases on the transcriptional machinery. The comparisons between GES profiles have been used to investigate the relationships between drugs, their targets and diseases with quite a few successful cases reported. Especially in the study of GES-guided drugs–disease associations, researchers believe that if a GES induced by a drug is opposite to a GES induced by a disease, the drug may have potential as a treatment of that disease. In this study, we data-mined the crowd extracted expression of differential signatures (CREEDS) database to evaluate the similarity between GES profiles from drugs and their indicated diseases. Our study aims to explore the application domains of GES-guided drug–disease associations through the analysis of the similarity of GES profiles on known pairs of drug–disease associations, thereby identifying subgroups of drugs/diseases that are suitable for GES-guided drug repositioning approaches. Our results supported our hypothesis that the GES-guided drug–disease association method is better suited for some subgroups or pathways such as drugs and diseases associated with the immune system, diseases of the nervous system, non-chemotherapy drugs or the mTOR signaling pathway. MDPI 2020-06-16 /pmc/articles/PMC7357095/ /pubmed/32560162 http://dx.doi.org/10.3390/molecules25122776 Text en © 2020 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 Qi, Xiguang Shen, Mingzhe Fan, Peihao Guo, Xiaojiang Wang, Tianqi Feng, Ning Zhang, Manling Sweet, Robert A. Kirisci, Levent Wang, Lirong The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases |
title | The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases |
title_full | The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases |
title_fullStr | The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases |
title_full_unstemmed | The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases |
title_short | The Performance of Gene Expression Signature-Guided Drug–Disease Association in Different Categories of Drugs and Diseases |
title_sort | performance of gene expression signature-guided drug–disease association in different categories of drugs and diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357095/ https://www.ncbi.nlm.nih.gov/pubmed/32560162 http://dx.doi.org/10.3390/molecules25122776 |
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