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Mapping the perturbome network of cellular perturbations
Drug combinations provide effective treatments for diverse diseases, but also represent a major cause of adverse reactions. Currently there is no systematic understanding of how the complex cellular perturbations induced by different drugs influence each other. Here, we introduce a mathematical fram...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853941/ https://www.ncbi.nlm.nih.gov/pubmed/31723137 http://dx.doi.org/10.1038/s41467-019-13058-9 |
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author | Caldera, Michael Müller, Felix Kaltenbrunner, Isabel Licciardello, Marco P. Lardeau, Charles-Hugues Kubicek, Stefan Menche, Jörg |
author_facet | Caldera, Michael Müller, Felix Kaltenbrunner, Isabel Licciardello, Marco P. Lardeau, Charles-Hugues Kubicek, Stefan Menche, Jörg |
author_sort | Caldera, Michael |
collection | PubMed |
description | Drug combinations provide effective treatments for diverse diseases, but also represent a major cause of adverse reactions. Currently there is no systematic understanding of how the complex cellular perturbations induced by different drugs influence each other. Here, we introduce a mathematical framework for classifying any interaction between perturbations with high-dimensional effects into 12 interaction types. We apply our framework to a large-scale imaging screen of cell morphology changes induced by diverse drugs and their combination, resulting in a perturbome network of 242 drugs and 1832 interactions. Our analysis of the chemical and biological features of the drugs reveals distinct molecular fingerprints for each interaction type. We find a direct link between drug similarities on the cell morphology level and the distance of their respective protein targets within the cellular interactome of molecular interactions. The interactome distance is also predictive for different types of drug interactions. |
format | Online Article Text |
id | pubmed-6853941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68539412019-11-18 Mapping the perturbome network of cellular perturbations Caldera, Michael Müller, Felix Kaltenbrunner, Isabel Licciardello, Marco P. Lardeau, Charles-Hugues Kubicek, Stefan Menche, Jörg Nat Commun Article Drug combinations provide effective treatments for diverse diseases, but also represent a major cause of adverse reactions. Currently there is no systematic understanding of how the complex cellular perturbations induced by different drugs influence each other. Here, we introduce a mathematical framework for classifying any interaction between perturbations with high-dimensional effects into 12 interaction types. We apply our framework to a large-scale imaging screen of cell morphology changes induced by diverse drugs and their combination, resulting in a perturbome network of 242 drugs and 1832 interactions. Our analysis of the chemical and biological features of the drugs reveals distinct molecular fingerprints for each interaction type. We find a direct link between drug similarities on the cell morphology level and the distance of their respective protein targets within the cellular interactome of molecular interactions. The interactome distance is also predictive for different types of drug interactions. Nature Publishing Group UK 2019-11-13 /pmc/articles/PMC6853941/ /pubmed/31723137 http://dx.doi.org/10.1038/s41467-019-13058-9 Text en © The Author(s) 2019 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 Caldera, Michael Müller, Felix Kaltenbrunner, Isabel Licciardello, Marco P. Lardeau, Charles-Hugues Kubicek, Stefan Menche, Jörg Mapping the perturbome network of cellular perturbations |
title | Mapping the perturbome network of cellular perturbations |
title_full | Mapping the perturbome network of cellular perturbations |
title_fullStr | Mapping the perturbome network of cellular perturbations |
title_full_unstemmed | Mapping the perturbome network of cellular perturbations |
title_short | Mapping the perturbome network of cellular perturbations |
title_sort | mapping the perturbome network of cellular perturbations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853941/ https://www.ncbi.nlm.nih.gov/pubmed/31723137 http://dx.doi.org/10.1038/s41467-019-13058-9 |
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