Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/88483
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorAzam, Z-
dc.creatorTo, SST-
dc.creatorTannous, BA-
dc.date.accessioned2020-11-27T05:49:40Z-
dc.date.available2020-11-27T05:49:40Z-
dc.identifier.issn2198-3844-
dc.identifier.urihttp://hdl.handle.net/10397/88483-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2020 The Authors. Published by Wiley‐VCH GmbHen_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Azam, Z., To, S. S. T., & Tannous, B. A. (2020). Mesenchymal Transformation: The Rosetta Stone of Glioblastoma Pathogenesis and Therapy Resistance. Advanced Science, 2002015, 1-13 is available at https://dx.doi.org/10.1002/advs.202002015en_US
dc.subjectClinical outcomeen_US
dc.subjectGlioblastoma (GBM)en_US
dc.subjectMesenchymal transitionen_US
dc.subjectMolecular subtypesen_US
dc.subjectTherapy responsesen_US
dc.subjectTumor microenvironmenten_US
dc.titleMesenchymal transformation : the rosetta stone of glioblastoma pathogenesis and therapy resistanceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1-
dc.identifier.epage13-
dc.identifier.doi10.1002/advs.202002015-
dcterms.abstractDespite decades of research, glioblastoma (GBM) remains invariably fatal among all forms of cancers. The high level of inter- and intratumoral heterogeneity along with its biological location, the brain, are major barriers against effective treatment. Molecular and single cell analysis identifies different molecular subtypes with varying prognosis, while multiple subtypes can reside in the same tumor. Cellular plasticity among different subtypes in response to therapies or during recurrence adds another hurdle in the treatment of GBM. This phenotypic shift is induced and sustained by activation of several pathways within the tumor itself, or microenvironmental factors. In this review, the dynamic nature of cellular shifts in GBM and how the tumor (immune) microenvironment shapes this process leading to therapeutic resistance, while highlighting emerging tools and approaches to study this dynamic double-edged sword are discussed.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced science, 2020, 2002015, p. 1-13-
dcterms.isPartOfAdvanced science-
dcterms.issued2020-
dc.identifier.isiWOS:000573151000001-
dc.identifier.scopus2-s2.0-85091613900-
dc.identifier.artn2002015-
dc.description.validate202011 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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