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Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach
In the present work, we apply a geometric network approach to study common biological features of anticancer drug response. We use for this purpose the panel of 60 human cell lines (NCI-60) provided by the National Cancer Institute. Our study suggests that mathematical tools for network-based analys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913269/ https://www.ncbi.nlm.nih.gov/pubmed/29686393 http://dx.doi.org/10.1038/s41598-018-24679-3 |
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author | Pouryahya, Maryam Oh, Jung Hun Mathews, James C. Deasy, Joseph O. Tannenbaum, Allen R. |
author_facet | Pouryahya, Maryam Oh, Jung Hun Mathews, James C. Deasy, Joseph O. Tannenbaum, Allen R. |
author_sort | Pouryahya, Maryam |
collection | PubMed |
description | In the present work, we apply a geometric network approach to study common biological features of anticancer drug response. We use for this purpose the panel of 60 human cell lines (NCI-60) provided by the National Cancer Institute. Our study suggests that mathematical tools for network-based analysis can provide novel insights into drug response and cancer biology. We adopted a discrete notion of Ricci curvature to measure, via a link between Ricci curvature and network robustness established by the theory of optimal mass transport, the robustness of biological networks constructed with a pre-treatment gene expression dataset and coupled the results with the GI50 response of the cell lines to the drugs. Based on the resulting drug response ranking, we assessed the impact of genes that are likely associated with individual drug response. For genes identified as important, we performed a gene ontology enrichment analysis using a curated bioinformatics database which resulted in biological processes associated with drug response across cell lines and tissue types which are plausible from the point of view of the biological literature. These results demonstrate the potential of using the mathematical network analysis in assessing drug response and in identifying relevant genomic biomarkers and biological processes for precision medicine. |
format | Online Article Text |
id | pubmed-5913269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59132692018-04-30 Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach Pouryahya, Maryam Oh, Jung Hun Mathews, James C. Deasy, Joseph O. Tannenbaum, Allen R. Sci Rep Article In the present work, we apply a geometric network approach to study common biological features of anticancer drug response. We use for this purpose the panel of 60 human cell lines (NCI-60) provided by the National Cancer Institute. Our study suggests that mathematical tools for network-based analysis can provide novel insights into drug response and cancer biology. We adopted a discrete notion of Ricci curvature to measure, via a link between Ricci curvature and network robustness established by the theory of optimal mass transport, the robustness of biological networks constructed with a pre-treatment gene expression dataset and coupled the results with the GI50 response of the cell lines to the drugs. Based on the resulting drug response ranking, we assessed the impact of genes that are likely associated with individual drug response. For genes identified as important, we performed a gene ontology enrichment analysis using a curated bioinformatics database which resulted in biological processes associated with drug response across cell lines and tissue types which are plausible from the point of view of the biological literature. These results demonstrate the potential of using the mathematical network analysis in assessing drug response and in identifying relevant genomic biomarkers and biological processes for precision medicine. Nature Publishing Group UK 2018-04-23 /pmc/articles/PMC5913269/ /pubmed/29686393 http://dx.doi.org/10.1038/s41598-018-24679-3 Text en © The Author(s) 2018 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 Pouryahya, Maryam Oh, Jung Hun Mathews, James C. Deasy, Joseph O. Tannenbaum, Allen R. Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach |
title | Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach |
title_full | Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach |
title_fullStr | Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach |
title_full_unstemmed | Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach |
title_short | Characterizing Cancer Drug Response and Biological Correlates: A Geometric Network Approach |
title_sort | characterizing cancer drug response and biological correlates: a geometric network approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913269/ https://www.ncbi.nlm.nih.gov/pubmed/29686393 http://dx.doi.org/10.1038/s41598-018-24679-3 |
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