Original Article

Oncogene (2008) 27, 2897–2909; doi:10.1038/sj.onc.1210949; published online 26 November 2007

Glioblastoma-derived stem cell-enriched cultures form distinct subgroups according to molecular and phenotypic criteria

H S Günther1,5, N O Schmidt1,5, H S Phillips2, D Kemming3, S Kharbanda2, R Soriano4, Z Modrusan4, H Meissner1, M Westphal1 and K Lamszus1

  1. 1Department of Neurosurgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
  2. 2Department of Tumor Biology and Angiogenesis, Genentech Inc., South San Francisco, CA, USA
  3. 3Institute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
  4. 4Department of Molecular Biology, Genentech Inc., South San Francisco, CA, USA

Correspondence: Dr K Lamszus, Laboratory for Brain Tumor Biology, Department of Neurosurgery, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, Hamburg 20246, Germany. E-mail: lamszus@uke.uni-hamburg.de

5These authors contributed equally to this work.

Received 4 September 2007; Revised 24 October 2007; Accepted 25 October 2007; Published online 26 November 2007.

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Abstract

Tumor cells with stem cell-like properties can be cultured from human glioblastomas by using conditions that select for the expansion of neural stem cells. We generated cell lines from glioblastoma specimens with the goal to obtain model systems for glioma stem cell biology. Unsupervised analysis of the expression profiles of nine cell lines established under neural stem cell conditions yielded two distinct clusters. Four cell lines were characterized by the expression of neurodevelopmental genes. They showed a multipotent differentiation profile along neuronal, astroglial and oligodendroglial lineages, grew spherically in vitro, expressed CD133 and formed highly invasive tumors in vivo. The other five cell lines shared expression signatures enriched for extracellular matrix-related genes, had a more restricted differentiation capacity, contained no or fewer CD133+ cells, grew semiadherent or adherent in vitro and displayed reduced tumorigenicity and invasion in vivo. Our findings show that stable, multipotent glioblastoma cell lines with a full stem-like phenotype express neurodevelopmental genes as a distinctive feature, which may offer therapeutic targeting opportunities. The generation of another distinct cluster of cell lines showing similarly homogeneous profiling but restricted stem cell properties suggests that different phenotypes exist, each of which may lead to the typical appearance of glioblastoma.

Keywords:

glioma, neural stem cell, neurosphere, microarray, pathway

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