Identifying Drug Sensitivity Subnetworks with NETPHIX
Summary: Phenotypic heterogeneity in cancer is often caused by different patterns of genetic alterations. Understanding such phenotype-genotype relationships is fundamental for the advance of personalized medicine. We develop a computational method, named NETPHIX (NETwork-to-PHenotype association wi...
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doaj-9beedc513935441ca394266f89892de92020-11-25T03:53:06ZengElsevieriScience2589-00422020-10-012310101619Identifying Drug Sensitivity Subnetworks with NETPHIXYoo-Ah Kim0Rebecca Sarto Basso1Damian Wojtowicz2Amanda S. Liu3Dorit S. Hochbaum4Fabio Vandin5Teresa M. Przytycka6National Center of Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD 20894, USA; Corresponding authorDepartment of Industrial Engineering and Operations Research, University of California at Berkeley, Berkeley, CA 94709, USANational Center of Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD 20894, USAMontgomery Blair High School, Silver Spring, MD 20901, USADepartment of Industrial Engineering and Operations Research, University of California at Berkeley, Berkeley, CA 94709, USADepartment of Information Engineering, University of Padova, Padova 35131, ItalyNational Center of Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD 20894, USA; Corresponding authorSummary: Phenotypic heterogeneity in cancer is often caused by different patterns of genetic alterations. Understanding such phenotype-genotype relationships is fundamental for the advance of personalized medicine. We develop a computational method, named NETPHIX (NETwork-to-PHenotype association with eXclusivity) to identify subnetworks of genes whose genetic alterations are associated with drug response or other continuous cancer phenotypes. Leveraging interaction information among genes and properties of cancer mutations such as mutual exclusivity, we formulate the problem as an integer linear program and solve it optimally to obtain a subnetwork of associated genes. Applied to a large-scale drug screening dataset, NETPHIX uncovered gene modules significantly associated with drug responses. Utilizing interaction information, NETPHIX modules are functionally coherent and can thus provide important insights into drug action. In addition, we show that modules identified by NETPHIX together with their association patterns can be leveraged to suggest drug combinations.http://www.sciencedirect.com/science/article/pii/S2589004220308117Biological SciencesBioinformaticsCancer Systems Biology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yoo-Ah Kim Rebecca Sarto Basso Damian Wojtowicz Amanda S. Liu Dorit S. Hochbaum Fabio Vandin Teresa M. Przytycka |
spellingShingle |
Yoo-Ah Kim Rebecca Sarto Basso Damian Wojtowicz Amanda S. Liu Dorit S. Hochbaum Fabio Vandin Teresa M. Przytycka Identifying Drug Sensitivity Subnetworks with NETPHIX iScience Biological Sciences Bioinformatics Cancer Systems Biology |
author_facet |
Yoo-Ah Kim Rebecca Sarto Basso Damian Wojtowicz Amanda S. Liu Dorit S. Hochbaum Fabio Vandin Teresa M. Przytycka |
author_sort |
Yoo-Ah Kim |
title |
Identifying Drug Sensitivity Subnetworks with NETPHIX |
title_short |
Identifying Drug Sensitivity Subnetworks with NETPHIX |
title_full |
Identifying Drug Sensitivity Subnetworks with NETPHIX |
title_fullStr |
Identifying Drug Sensitivity Subnetworks with NETPHIX |
title_full_unstemmed |
Identifying Drug Sensitivity Subnetworks with NETPHIX |
title_sort |
identifying drug sensitivity subnetworks with netphix |
publisher |
Elsevier |
series |
iScience |
issn |
2589-0042 |
publishDate |
2020-10-01 |
description |
Summary: Phenotypic heterogeneity in cancer is often caused by different patterns of genetic alterations. Understanding such phenotype-genotype relationships is fundamental for the advance of personalized medicine. We develop a computational method, named NETPHIX (NETwork-to-PHenotype association with eXclusivity) to identify subnetworks of genes whose genetic alterations are associated with drug response or other continuous cancer phenotypes. Leveraging interaction information among genes and properties of cancer mutations such as mutual exclusivity, we formulate the problem as an integer linear program and solve it optimally to obtain a subnetwork of associated genes. Applied to a large-scale drug screening dataset, NETPHIX uncovered gene modules significantly associated with drug responses. Utilizing interaction information, NETPHIX modules are functionally coherent and can thus provide important insights into drug action. In addition, we show that modules identified by NETPHIX together with their association patterns can be leveraged to suggest drug combinations. |
topic |
Biological Sciences Bioinformatics Cancer Systems Biology |
url |
http://www.sciencedirect.com/science/article/pii/S2589004220308117 |
work_keys_str_mv |
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