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dc.contributor.authorQin, EY
dc.contributor.authorCooper, DD
dc.contributor.authorAbbott, KL
dc.contributor.authorLennon, J
dc.contributor.authorNagaraja, S
dc.contributor.authorMackay, A
dc.contributor.authorJones, C
dc.contributor.authorVogel, H
dc.contributor.authorJackson, PK
dc.contributor.authorMonje, M
dc.date.accessioned2017-08-31T13:40:39Z
dc.date.issued2017-08-24
dc.identifier.citationCell, 2017, 170 (5), pp. 845 - 859.e19
dc.identifier.issn0092-8674
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/804
dc.identifier.eissn1097-4172
dc.identifier.doi10.1016/j.cell.2017.07.016
dc.description.abstractThe lateral ventricle subventricular zone (SVZ) is a frequent and consequential site of pediatric and adult glioma spread, but the cellular and molecular mechanisms mediating this are poorly understood. We demonstrate that neural precursor cell (NPC):glioma cell communication underpins this propensity of glioma to colonize the SVZ through secretion of chemoattractant signals toward which glioma cells home. Biochemical, proteomic, and functional analyses of SVZ NPC-secreted factors revealed the neurite outgrowth-promoting factor pleiotrophin, along with required binding partners SPARC/SPARCL1 and HSP90B, as key mediators of this chemoattractant effect. Pleiotrophin expression is strongly enriched in the SVZ, and pleiotrophin knock down starkly reduced glioma invasion of the SVZ in the murine brain. Pleiotrophin, in complex with the binding partners, activated glioma Rho/ROCK signaling, and ROCK inhibition decreased invasion toward SVZ NPC-secreted factors. These findings demonstrate a pathogenic role for NPC:glioma interactions and potential therapeutic targets to limit glioma invasion. PAPERCLIP.
dc.formatPrint-Electronic
dc.format.extent845 - 859.e19
dc.languageeng
dc.language.isoeng
dc.publisherCELL PRESS
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectLateral Ventricles
dc.subjectAnimals
dc.subjectHumans
dc.subjectMice
dc.subjectGlioma
dc.subjectBrain Neoplasms
dc.subjectNeoplasm Invasiveness
dc.subjectrho GTP-Binding Proteins
dc.subjectCarrier Proteins
dc.subjectCytokines
dc.subjectDrug Delivery Systems
dc.subjectNeoplasm Transplantation
dc.subjectCell Communication
dc.subjectSignal Transduction
dc.subjectAged
dc.subjectChild
dc.subjectFemale
dc.subjectMale
dc.subjectHSP90 Heat-Shock Proteins
dc.subjectHeterografts
dc.titleNeural Precursor-Derived Pleiotrophin Mediates Subventricular Zone Invasion by Glioma.
dc.typeJournal Article
dcterms.dateAccepted2017-07-13
rioxxterms.funderThe Institute of Cancer Research
rioxxterms.identifier.projectUnspecified
rioxxterms.versionofrecord10.1016/j.cell.2017.07.016
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-08-17
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCell
pubs.issue5
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Glioma Team
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Glioma Team
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Glioma Team
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Glioma Team
pubs.publication-statusPublished
pubs.volume170
pubs.embargo.termsNot known
icr.researchteamGlioma Team
dc.contributor.icrauthorMackay, Alan
dc.contributor.icrauthorJones, Chris


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