| Literature DB >> 31901251 |
Aparna Bhaduri1, Elizabeth Di Lullo1, Diane Jung1, Sören Müller2, Elizabeth Erin Crouch3, Carmen Sandoval Espinosa1, Tomoko Ozawa4, Beatriz Alvarado1, Julien Spatazza5, Cathryn René Cadwell6, Grace Wilkins1, Dmitry Velmeshev1, Siyuan John Liu5, Martina Malatesta5, Madeline Gail Andrews1, Mohammed Andres Mostajo-Radji1, Eric Jinsheng Huang6, Tomasz Jan Nowakowski7, Daniel Amos Lim5, Aaron Diaz2, David Ronan Raleigh8, Arnold Richard Kriegstein9.
Abstract
Glioblastoma is a devastating form of brain cancer. To identify aspects of tumor heterogeneity that may illuminate drivers of tumor invasion, we created a glioblastoma tumor cell atlas with single-cell transcriptomics of cancer cells mapped onto a reference framework of the developing and adult human brain. We find that multiple GSC subtypes exist within a single tumor. Within these GSCs, we identify an invasive cell population similar to outer radial glia (oRG), a fetal cell type that expands the stem cell niche in normal human cortex. Using live time-lapse imaging of primary resected tumors, we discover that tumor-derived oRG-like cells undergo characteristic mitotic somal translocation behavior previously only observed in human development, suggesting a reactivation of developmental programs. In addition, we show that PTPRZ1 mediates both mitotic somal translocation and glioblastoma tumor invasion. These data suggest that the presence of heterogeneous GSCs may underlie glioblastoma's rapid progression and invasion. Published by Elsevier Inc.Entities:
Keywords: cancer stem cell; glioblastoma; outer radial glia; single-cell sequencing; tumor heterogeneity
Mesh:
Substances:
Year: 2020 PMID: 31901251 PMCID: PMC7029801 DOI: 10.1016/j.stem.2019.11.015
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633