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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Main Authors: Yoo-Ah Kim, Rebecca Sarto Basso, Damian Wojtowicz, Amanda S. Liu, Dorit S. Hochbaum, Fabio Vandin, Teresa M. Przytycka
Format: Article
Language:English
Published: Elsevier 2020-10-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004220308117
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spelling 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
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