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Outer Radial Glia-like Cancer Stem Cells Contribute to Heterogeneity of Glioblastoma.
Citation | “Outer Radial Glia-Like Cancer Stem Cells Contribute To Heterogeneity Of Glioblastoma.”. Cell Stem Cell, pp. 48-63.e6. . |
Author | Aparna Bhaduri, Elizabeth Di Lullo, Diane Jung, Sören Müller, Elizabeth Erin Crouch, Carmen Sandoval Espinosa, Tomoko Ozawa, Beatriz Alvarado, Julien Spatazza, Cathryn René Cadwell, Grace Wilkins, Dmitry Velmeshev, Siyuan John Liu, Martina Malatesta, Madeline Gail Andrews, Mohammed Andres Mostajo-Radji, Eric Jinsheng Huang, Tomasz Jan Nowakowski, Daniel Amos Lim, Aaron Diaz, David Ronan Raleigh, Arnold Richard Kriegstein |
Keywords | cancer stem cell, glioblastoma, outer radial glia, single-cell sequencing, tumor heterogeneity |
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. |
Year of Publication |
2020
|
Journal |
Cell stem cell
|
Volume |
26
|
Issue |
1
|
Number of Pages |
48-63.e6
|
Date Published |
01/2020
|
ISSN Number |
1875-9777
|
DOI |
10.1016/j.stem.2019.11.015
|
Alternate Journal |
Cell Stem Cell
|
PMID |
31901251
|
PMCID |
PMC7029801
|
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