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      Single-Cell RNA-Seq Analysis of Infiltrating Neoplastic Cells at the Migrating Front of Human Glioblastoma

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          SUMMARY

          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.

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          Author and article information

          Journal
          101573691
          39703
          Cell Rep
          Cell Rep
          Cell reports
          2211-1247
          8 February 2018
          31 October 2017
          13 February 2018
          : 21
          : 5
          : 1399-1410
          Affiliations
          [1 ]Departments of Bioengineering and Applied Physics, Stanford University and Chan Zuckerberg Biohub, 318 Campus Drive, Stanford, CA 94305, USA
          [2 ]Department of Neurobiology, Stanford University, 291 Campus Drive, Stanford, CA 94305, USA
          [3 ]Department of Neurosurgery, Stanford University, 300 Pasteur Drive, Stanford, CA 94304, USA
          [4 ]Department of Pathology, Stanford University, 300 Pasteur Drive, Stanford, CA 94304, USA
          [5 ]These authors contributed equally
          Author notes
          [* ]Correspondence: quake@ 123456stanford.edu
          [6]

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          Article
          PMC5810554 PMC5810554 5810554 nihpa938967
          10.1016/j.celrep.2017.10.030
          5810554
          29091775
          5a444342-c406-4d4d-8c9b-c3329c0e1710
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