| Literature DB >> 32649888 |
Zilai Wang1, Daochun Sun1, Yu-Jung Chen2, Xuanhua Xie1, Yufeng Shi1, Viviane Tabar3, Cameron W Brennan3, Tejus A Bale4, Chenura D Jayewickreme5, Dan R Laks1, Sheila Alcantara Llaguno1, Luis F Parada6.
Abstract
Glioblastoma, the predominant adult malignant brain tumor, has been computationally classified into molecular subtypes whose functional relevance remains to be comprehensively established. Tumors from genetically engineered glioblastoma mouse models initiated by identical driver mutations in distinct cells of origin portray unique transcriptional profiles reflective of their respective lineage. Here, we identify corresponding transcriptional profiles in human glioblastoma and describe patient-derived xenografts with species-conserved subtype-discriminating functional properties. The oligodendrocyte lineage-associated glioblastoma subtype requires functional ERBB3 and harbors unique therapeutic sensitivities. These results highlight the importance of cell lineage in glioblastoma independent of driver mutations and provide a methodology for functional glioblastoma classification for future clinical investigations.Entities:
Keywords: Erbb3; GBM; PDX; cell of origin; glioblastoma; molecular classification; molecular subtype; mouse model; neural stem cell; oligodendrocyte lineage cell
Mesh:
Substances:
Year: 2020 PMID: 32649888 PMCID: PMC7494533 DOI: 10.1016/j.ccell.2020.06.003
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743