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PRER: A patient representation with pairwise relative expression of proteins on biological networks
Changes in protein and gene expression levels are often used as features in predictive modeling such as survival prediction. A common strategy to aggregate information contained in individual proteins is to integrate the expression levels with the biological networks. In this work, we propose a nove...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238204/ https://www.ncbi.nlm.nih.gov/pubmed/34038408 http://dx.doi.org/10.1371/journal.pcbi.1008998 |
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author | Kuru, Halil İbrahim Buyukozkan, Mustafa Tastan, Oznur |
author_facet | Kuru, Halil İbrahim Buyukozkan, Mustafa Tastan, Oznur |
author_sort | Kuru, Halil İbrahim |
collection | PubMed |
description | Changes in protein and gene expression levels are often used as features in predictive modeling such as survival prediction. A common strategy to aggregate information contained in individual proteins is to integrate the expression levels with the biological networks. In this work, we propose a novel patient representation where we integrate proteins’ expression levels with the protein-protein interaction (PPI) networks: Patient representation with PRER (Pairwise Relative Expressions with Random walks). PRER captures the dysregulation patterns of proteins based on the neighborhood of a protein in the PPI network. Specifically, PRER computes a feature vector for a patient by comparing the source protein’s expression level with other proteins’ levels that are within its neighborhood. The neighborhood of the source protein is derived by biased random-walk strategy on the network. We test PRER’s performance in survival prediction task in 10 different cancers using random forest survival models. PRER yields a statistically significant predictive performance in 9 out of 10 cancers when compared to the same model trained with features based on individual protein expressions. Furthermore, we identified the pairs of proteins that their interactions are predictive of patient survival but their individual expression levels are not. The set of identified relations provides a valuable collection of protein biomarkers with high prognostic value. PRER can be used for other complex diseases and prediction tasks that use molecular expression profiles as input. PRER is freely available at: https://github.com/hikuru/PRER. |
format | Online Article Text |
id | pubmed-8238204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-82382042021-07-09 PRER: A patient representation with pairwise relative expression of proteins on biological networks Kuru, Halil İbrahim Buyukozkan, Mustafa Tastan, Oznur PLoS Comput Biol Research Article Changes in protein and gene expression levels are often used as features in predictive modeling such as survival prediction. A common strategy to aggregate information contained in individual proteins is to integrate the expression levels with the biological networks. In this work, we propose a novel patient representation where we integrate proteins’ expression levels with the protein-protein interaction (PPI) networks: Patient representation with PRER (Pairwise Relative Expressions with Random walks). PRER captures the dysregulation patterns of proteins based on the neighborhood of a protein in the PPI network. Specifically, PRER computes a feature vector for a patient by comparing the source protein’s expression level with other proteins’ levels that are within its neighborhood. The neighborhood of the source protein is derived by biased random-walk strategy on the network. We test PRER’s performance in survival prediction task in 10 different cancers using random forest survival models. PRER yields a statistically significant predictive performance in 9 out of 10 cancers when compared to the same model trained with features based on individual protein expressions. Furthermore, we identified the pairs of proteins that their interactions are predictive of patient survival but their individual expression levels are not. The set of identified relations provides a valuable collection of protein biomarkers with high prognostic value. PRER can be used for other complex diseases and prediction tasks that use molecular expression profiles as input. PRER is freely available at: https://github.com/hikuru/PRER. Public Library of Science 2021-05-26 /pmc/articles/PMC8238204/ /pubmed/34038408 http://dx.doi.org/10.1371/journal.pcbi.1008998 Text en © 2021 Kuru et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kuru, Halil İbrahim Buyukozkan, Mustafa Tastan, Oznur PRER: A patient representation with pairwise relative expression of proteins on biological networks |
title | PRER: A patient representation with pairwise relative expression of proteins on biological networks |
title_full | PRER: A patient representation with pairwise relative expression of proteins on biological networks |
title_fullStr | PRER: A patient representation with pairwise relative expression of proteins on biological networks |
title_full_unstemmed | PRER: A patient representation with pairwise relative expression of proteins on biological networks |
title_short | PRER: A patient representation with pairwise relative expression of proteins on biological networks |
title_sort | prer: a patient representation with pairwise relative expression of proteins on biological networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238204/ https://www.ncbi.nlm.nih.gov/pubmed/34038408 http://dx.doi.org/10.1371/journal.pcbi.1008998 |
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