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      Zika virus has oncolytic activity against glioblastoma stem cells

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          Abstract

          Zhu et al. show that the Zika virus, which has a tropism for fetal and adult neuroprogenitor cells, targets and kills cancer stem cells while leaving differentiated tumor cells relatively unaffected, providing a new potential oncolytic virus therapy in neuro-oncology.

          Abstract

          Glioblastoma is a highly lethal brain cancer that frequently recurs in proximity to the original resection cavity. We explored the use of oncolytic virus therapy against glioblastoma with Zika virus (ZIKV), a flavivirus that induces cell death and differentiation of neural precursor cells in the developing fetus. ZIKV preferentially infected and killed glioblastoma stem cells (GSCs) relative to differentiated tumor progeny or normal neuronal cells. The effects against GSCs were not a general property of neurotropic flaviviruses, as West Nile virus indiscriminately killed both tumor and normal neural cells. ZIKV potently depleted patient-derived GSCs grown in culture and in organoids. Moreover, mice with glioblastoma survived substantially longer and at greater rates when the tumor was inoculated with a mouse-adapted strain of ZIKV. Our results suggest that ZIKV is an oncolytic virus that can preferentially target GSCs; thus, genetically modified strains that further optimize safety could have therapeutic efficacy for adult glioblastoma patients.

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          A restricted cell population propagates glioblastoma growth following chemotherapy

          Glioblastoma multiforme (GBM) is the most common primary malignant brain tumor, with a median survival of about one year 1 . This poor prognosis is due to therapeutic resistance and tumor recurrence following surgical removal. Precisely how recurrence occurs is unknown. Using a genetically-engineered mouse model of glioma, we identify a subset of endogenous tumor cells that are the source of new tumor cells after the drug, temozolomide (TMZ), is administered to transiently arrest tumor growth. A Nestin-ΔTK-IRES-GFP (Nes-ΔTK-GFP) transgene that labels quiescent subventricular zone adult neural stem cells also labels a subset of endogenous glioma tumor cells. Upon arrest of tumor cell proliferation with TMZ, pulse-chase experiments demonstrate a tumor re-growth cell hierarchy originating with the Nes-ΔTK-GFP transgene subpopulation. Ablation of the GFP+ cells with chronic ganciclovir administration significantly arrested tumor growth and combined TMZ-ganciclovir treatment impeded tumor development. These data indicate the existence of a relatively quiescent subset of endogenous glioma cells that are responsible for sustaining long-term tumor growth through the production of transient populations of highly proliferative cells.
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            Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system.

            Neurogenesis in the mammalian central nervous system is believed to end in the period just after birth; in the mouse striatum no new neurons are produced after the first few days after birth. In this study, cells isolated from the striatum of the adult mouse brain were induced to proliferate in vitro by epidermal growth factor. The proliferating cells initially expressed nestin, an intermediate filament found in neuroepithelial stem cells, and subsequently developed the morphology and antigenic properties of neurons and astrocytes. Newly generated cells with neuronal morphology were immunoreactive for gamma-aminobutyric acid and substance P, two neurotransmitters of the adult striatum in vivo. Thus, cells of the adult mouse striatum have the capacity to divide and differentiate into neurons and astrocytes.
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              Reconstructing and reprogramming the tumor-propagating potential of glioblastoma stem-like cells.

              Developmental fate decisions are dictated by master transcription factors (TFs) that interact with cis-regulatory elements to direct transcriptional programs. Certain malignant tumors may also depend on cellular hierarchies reminiscent of normal development but superimposed on underlying genetic aberrations. In glioblastoma (GBM), a subset of stem-like tumor-propagating cells (TPCs) appears to drive tumor progression and underlie therapeutic resistance yet remain poorly understood. Here, we identify a core set of neurodevelopmental TFs (POU3F2, SOX2, SALL2, and OLIG2) essential for GBM propagation. These TFs coordinately bind and activate TPC-specific regulatory elements and are sufficient to fully reprogram differentiated GBM cells to "induced" TPCs, recapitulating the epigenetic landscape and phenotype of native TPCs. We reconstruct a network model that highlights critical interactions and identifies candidate therapeutic targets for eliminating TPCs. Our study establishes the epigenetic basis of a developmental hierarchy in GBM, provides detailed insight into underlying gene regulatory programs, and suggests attendant therapeutic strategies. PAPERCLIP: Copyright © 2014 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                J Exp Med
                J. Exp. Med
                jem
                jem
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                02 October 2017
                : 214
                : 10
                : 2843-2857
                Affiliations
                [1 ]Department of Medicine, Division of Regenerative Medicine, University of California, San Diego, School of Medicine, La Jolla, CA
                [2 ]Department of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH
                [3 ]Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO
                [4 ]Department of Medicine, Washington University School of Medicine, St. Louis, MO
                [5 ]Department of Neurology, Washington University School of Medicine, St. Louis, MO
                [6 ]Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO
                [7 ]The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO
                [8 ]Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX
                [9 ]Department of Pharmacology and Toxicology, Sealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch, Galveston, TX
                [10 ]Genome Technology Access Center, Department of Genetics, Washington University in St. Louis, St. Louis, MO
                Author notes
                Correspondence to Michael S. Diamond: diamond@ 123456wusm.wustl.edu ;
                Milan G. Chheda: mchheda@ 123456wustl.edu
                Author information
                http://orcid.org/0000-0002-5385-948X
                http://orcid.org/0000-0003-2560-8218
                http://orcid.org/0000-0002-5993-9368
                http://orcid.org/0000-0002-6646-6781
                http://orcid.org/0000-0001-8282-9098
                Article
                20171093
                10.1084/jem.20171093
                5626408
                28874392
                339612ac-8d22-4a4f-99b1-6276561cf0b2
                © 2017 Zhu et al.

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).

                History
                : 17 June 2017
                : 30 July 2017
                : 09 August 2017
                Funding
                Funded by: National Institutes of Health, DOI http://dx.doi.org/10.13039/100000002;
                Award ID: R01 AI073755
                Award ID: R01 AI104972
                Award ID: CA197718
                Award ID: CA154130
                Award ID: CA169117
                Award ID: CA171652
                Award ID: NS087913
                Award ID: NS089272
                Funded by: Elsa U. Pardee Foundation, DOI http://dx.doi.org/10.13039/100001287;
                Funded by: Concern Foundation, DOI http://dx.doi.org/10.13039/100001558;
                Funded by: Cancer Research Foundation, DOI http://dx.doi.org/10.13039/100002002;
                Funded by: Washington University, DOI http://dx.doi.org/10.13039/100007268;
                Funded by: NCI, DOI http://dx.doi.org/10.13039/100000054;
                Award ID: P50 CA094056
                Funded by: NCI, DOI http://dx.doi.org/10.13039/100000054;
                Award ID: P30 CA91842
                Funded by: National Center for Research Resources, DOI http://dx.doi.org/10.13039/100000097;
                Award ID: UL1TR000448
                Funded by: NIH, DOI http://dx.doi.org/10.13039/100000002;
                Funded by: National Center for Advancing Translational Sciences, DOI http://dx.doi.org/10.13039/100006108;
                Award ID: UL1 TR002345
                Categories
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