| Literature DB >> 29091775 |
Spyros Darmanis1, Steven A Sloan2, Derek Croote1, Marco Mignardi1, Sophia Chernikova3, Peyman Samghababi4, Ye Zhang2, Norma Neff1, Mark Kowarsky1, Christine Caneda2, Gordon Li3, Steven D Chang3, Ian David Connolly3, Yingmei Li3, Ben A Barres2, Melanie Hayden Gephart3, Stephen R Quake5.
Abstract
Glioblastoma (GBM) is the most common primary brain cancer in adults and is notoriously difficult to treat because of its diffuse nature. We performed single-cell RNA sequencing (RNA-seq) on 3,589 cells in a cohort of four patients. We obtained cells from the tumor core as well as surrounding peripheral tissue. Our analysis revealed cellular variation in the tumor's genome and transcriptome. We were also able to identify infiltrating neoplastic cells in regions peripheral to the core lesions. Despite the existence of significant heterogeneity among neoplastic cells, we found that infiltrating GBM cells share a consistent gene signature between patients, suggesting a common mechanism of infiltration. Additionally, in investigating the immunological response to the tumors, we found transcriptionally distinct myeloid cell populations residing in the tumor core and the surrounding peritumoral space. Our data provide a detailed dissection of GBM cell types, revealing an abundance of information about tumor formation and migration.Entities:
Keywords: GBM; RNA-seq; brain; checkpoint; diffuse; glioblastoma; glioma; heterogeneity; infiltrating; single cell
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Year: 2017 PMID: 29091775 PMCID: PMC5810554 DOI: 10.1016/j.celrep.2017.10.030
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423