Drug and disease signature integration identifies synergistic combinations in glioblastoma

Inherent or acquired resistance to treatment of glioblastoma (GBM) is nearly universal. Here, the authors introduce a platform to identify synergistic drug combinations for patient-specific treatment of GBM based on gene expression signatures and small molecule perturbation-response profiles.

Bibliographic Details
Main Authors: Vasileios Stathias, Anna M. Jermakowicz, Marie E. Maloof, Michele Forlin, Winston Walters, Robert K. Suter, Michael A. Durante, Sion L. Williams, J. William Harbour, Claude-Henry Volmar, Nicholas J. Lyons, Claes Wahlestedt, Regina M. Graham, Michael E. Ivan, Ricardo J. Komotar, Jann N. Sarkaria, Aravind Subramanian, Todd R. Golub, Stephan C. Schürer, Nagi G. Ayad
Format: Article
Language:English
Published: Nature Publishing Group 2018-12-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-018-07659-z
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spelling doaj-27c294a5f7c843d6a3a8dc34a08977c62021-05-11T10:28:12ZengNature Publishing GroupNature Communications2041-17232018-12-019111310.1038/s41467-018-07659-zDrug and disease signature integration identifies synergistic combinations in glioblastomaVasileios Stathias0Anna M. Jermakowicz1Marie E. Maloof2Michele Forlin3Winston Walters4Robert K. Suter5Michael A. Durante6Sion L. Williams7J. William Harbour8Claude-Henry Volmar9Nicholas J. Lyons10Claes Wahlestedt11Regina M. Graham12Michael E. Ivan13Ricardo J. Komotar14Jann N. Sarkaria15Aravind Subramanian16Todd R. Golub17Stephan C. Schürer18Nagi G. Ayad19Center for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineCenter for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineCenter for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineDepartment of Molecular and Cellular Pharmacology, Center for Computational Science, University of Miami Miller School of MedicineUniversity of Miami Brain Tumor Initiative, Department of Neurosurgery, University of Miami Miller School of MedicineSylvester Comprehensive Cancer Center, University of Miami Miller School of MedicineBascom Palmer Eye Institute, Sylvester Comprehensive Cancer Center, Interdisciplinary Stem Cell Institute, University of Miami Miller School of MedicineSylvester Comprehensive Cancer Center, University of Miami Miller School of MedicineBascom Palmer Eye Institute, Sylvester Comprehensive Cancer Center, Interdisciplinary Stem Cell Institute, University of Miami Miller School of MedicineCenter for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineBroad Institute of Harvard and MITCenter for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineSylvester Comprehensive Cancer Center, University of Miami Miller School of MedicineSylvester Comprehensive Cancer Center, University of Miami Miller School of MedicineSylvester Comprehensive Cancer Center, University of Miami Miller School of MedicineDepartment of Radiation Oncology, Mayo ClinicBroad Institute of Harvard and MITBroad Institute of Harvard and MITCenter for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineCenter for Therapeutic Innovation, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of MedicineInherent or acquired resistance to treatment of glioblastoma (GBM) is nearly universal. Here, the authors introduce a platform to identify synergistic drug combinations for patient-specific treatment of GBM based on gene expression signatures and small molecule perturbation-response profiles.https://doi.org/10.1038/s41467-018-07659-z
collection DOAJ
language English
format Article
sources DOAJ
author Vasileios Stathias
Anna M. Jermakowicz
Marie E. Maloof
Michele Forlin
Winston Walters
Robert K. Suter
Michael A. Durante
Sion L. Williams
J. William Harbour
Claude-Henry Volmar
Nicholas J. Lyons
Claes Wahlestedt
Regina M. Graham
Michael E. Ivan
Ricardo J. Komotar
Jann N. Sarkaria
Aravind Subramanian
Todd R. Golub
Stephan C. Schürer
Nagi G. Ayad
spellingShingle Vasileios Stathias
Anna M. Jermakowicz
Marie E. Maloof
Michele Forlin
Winston Walters
Robert K. Suter
Michael A. Durante
Sion L. Williams
J. William Harbour
Claude-Henry Volmar
Nicholas J. Lyons
Claes Wahlestedt
Regina M. Graham
Michael E. Ivan
Ricardo J. Komotar
Jann N. Sarkaria
Aravind Subramanian
Todd R. Golub
Stephan C. Schürer
Nagi G. Ayad
Drug and disease signature integration identifies synergistic combinations in glioblastoma
Nature Communications
author_facet Vasileios Stathias
Anna M. Jermakowicz
Marie E. Maloof
Michele Forlin
Winston Walters
Robert K. Suter
Michael A. Durante
Sion L. Williams
J. William Harbour
Claude-Henry Volmar
Nicholas J. Lyons
Claes Wahlestedt
Regina M. Graham
Michael E. Ivan
Ricardo J. Komotar
Jann N. Sarkaria
Aravind Subramanian
Todd R. Golub
Stephan C. Schürer
Nagi G. Ayad
author_sort Vasileios Stathias
title Drug and disease signature integration identifies synergistic combinations in glioblastoma
title_short Drug and disease signature integration identifies synergistic combinations in glioblastoma
title_full Drug and disease signature integration identifies synergistic combinations in glioblastoma
title_fullStr Drug and disease signature integration identifies synergistic combinations in glioblastoma
title_full_unstemmed Drug and disease signature integration identifies synergistic combinations in glioblastoma
title_sort drug and disease signature integration identifies synergistic combinations in glioblastoma
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2018-12-01
description Inherent or acquired resistance to treatment of glioblastoma (GBM) is nearly universal. Here, the authors introduce a platform to identify synergistic drug combinations for patient-specific treatment of GBM based on gene expression signatures and small molecule perturbation-response profiles.
url https://doi.org/10.1038/s41467-018-07659-z
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