Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/5075
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dc.contributor.authorDrakulić, Danijelaen_US
dc.contributor.authorSchwirtlich Marijaen_US
dc.contributor.authorPetrović Isidoraen_US
dc.contributor.authorMojsin, Marijaen_US
dc.contributor.authorMilivojević, Milenaen_US
dc.contributor.authorKovačević-Grujičić, Natašaen_US
dc.contributor.authorStevanović, Milenaen_US
dc.date.accessioned2022-11-15T09:03:59Z-
dc.date.available2022-11-15T09:03:59Z-
dc.date.issued2022-08-15-
dc.identifier.citationDrakulic D, Schwirtlich M, Petrovic I, Mojsin M, Milivojevic M, Kovacevic-Grujicic N, Stevanovic M. Current Opportunities for Targeting Dysregulated Neurodevelopmental Signaling Pathways in Glioblastoma. Cells. 2022 Aug 15;11(16):2530. doi: 10.3390/cells11162530. PMID: 36010607; PMCID: PMC9406959.en_US
dc.identifier.issn2073-4409-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/5075-
dc.description.abstractGlioblastoma (GBM) is the most common and highly lethal type of brain tumor, with poor survival despite advances in understanding its complexity. After current standard therapeutic treatment, including tumor resection, radiotherapy and concomitant chemotherapy with temozolomide, the median overall survival of patients with this type of tumor is less than 15 months. Thus, there is an urgent need for new insights into GBM molecular characteristics and progress in targeted therapy in order to improve clinical outcomes. The literature data revealed that a number of different signaling pathways are dysregulated in GBM. In this review, we intended to summarize and discuss current literature data and therapeutic modalities focused on targeting dysregulated signaling pathways in GBM. A better understanding of opportunities for targeting signaling pathways that influences malignant behavior of GBM cells might open the way for the development of novel GBM-targeted therapies.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofCellsen_US
dc.subjectGlioblastomaen_US
dc.subjectGBM subtypesen_US
dc.subjectSHH signalingen_US
dc.subjectWnt/β-catenin signalingen_US
dc.subjectNotch signalingen_US
dc.subjectTGFβ signalingen_US
dc.subjectBMP signalingen_US
dc.subjectHippo signalingen_US
dc.subjectRA signalingen_US
dc.titleCurrent opportunities for targeting dysregulated neurodevelopmental signaling pathways in glioblastomaen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/cells11162530-
dc.identifier.urlhttps://www.mdpi.com/2073-4409/11/16/2530/htm-
dc.description.rankM21en_US
dc.description.impact7.666en_US
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0003-4286-7334-
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