Please use this identifier to cite or link to this item:
https://scholarhub.balamand.edu.lb/handle/uob/7304
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hawly, Joseph | en_US |
dc.contributor.author | Murcar, Micaela G | en_US |
dc.contributor.author | Schcolnik-Cabrera, Alejandro | en_US |
dc.contributor.author | Issa, Mark E | en_US |
dc.date.accessioned | 2024-04-04T06:38:04Z | - |
dc.date.available | 2024-04-04T06:38:04Z | - |
dc.date.issued | 2024-03-26 | - |
dc.identifier.issn | 01677659 | - |
dc.identifier.uri | https://scholarhub.balamand.edu.lb/handle/uob/7304 | - |
dc.description.abstract | Despite enormous efforts being invested in the development of novel therapies for brain malignancies, there remains a dire need for effective treatments, particularly for pediatric glioblastomas. Their poor prognosis has been attributed to the fact that conventional therapies target tumoral cells, but not glioblastoma stem cells (GSCs). GSCs are characterized by self-renewal, tumorigenicity, poor differentiation, and resistance to therapy. These characteristics represent the fundamental tools needed to recapitulate the tumor and result in a relapse. The mechanisms by which GSCs alter metabolic cues and escape elimination by immune cells are discussed in this article, along with potential strategies to harness effector immune cells against GSCs. As cellular immunotherapy is making significant advances in a variety of cancers, leveraging this underexplored reservoir may result in significant improvements in the treatment options for brain malignancies. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Brain tumors | en_US |
dc.subject | Cancer metabolism | en_US |
dc.subject | Cancer stem cells | en_US |
dc.subject | Elimination | en_US |
dc.subject | Equilibrium | en_US |
dc.subject | Escape | en_US |
dc.subject | Immunoediting | en_US |
dc.subject | Immunotherapy | en_US |
dc.subject | Microglia | en_US |
dc.subject | Natural killer cells | en_US |
dc.subject | Resistance | en_US |
dc.subject | Self-renewal | en_US |
dc.subject | Surveillance | en_US |
dc.subject | T cells | en_US |
dc.subject | Tumorigenicity | en_US |
dc.title | Glioblastoma stem cell metabolism and immunity | en_US |
dc.type | Journal Article | en_US |
dc.identifier.doi | 10.1007/s10555-024-10183-w | - |
dc.identifier.pmid | 38530545 | - |
dc.identifier.scopus | 2-s2.0-85188734710 | - |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/85188734710 | - |
dc.contributor.affiliation | Faculty of Medicine | en_US |
dc.date.catalogued | 2024-04-04 | - |
dc.description.status | In Press | en_US |
dc.identifier.ezproxyURL | http://ezsecureaccess.balamand.edu.lb/login?url=https://link.springer.com/article/10.1007/s10555-024-10183-w | en_US |
dc.relation.ispartoftext | Cancer and Metastasis Reviews | en_US |
Appears in Collections: | Faculty of Medicine |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.