4.8 Article

Dedifferentiation of Neurons and Astrocytes by Oncogenes Can Induce Gliomas in Mice

Journal

SCIENCE
Volume 338, Issue 6110, Pages 1080-1084

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1226929

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Funding

  1. American Cancer Society Professor of Molecular Biology
  2. National Institutes of Health (NIH) [HL053670]
  3. Cancer Center Core Grant [P30 CA014195-38]
  4. Ipsen/Biomeasure
  5. Sanofi Aventis
  6. H. N. and Frances C. Berger Foundation
  7. National Center for Research Resources [5P41RR004050]

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Glioblastoma multiforme (GBM) is the most common and aggressive malignant primary brain tumor in humans. Here we show that gliomas can originate from differentiated cells in the central nervous system (CNS), including cortical neurons. Transduction by oncogenic lentiviral vectors of neural stem cells (NSCs), astrocytes, or even mature neurons in the brains of mice can give rise to malignant gliomas. All the tumors, irrespective of the site of lentiviral vector injection (the initiating population), shared common features of high expression of stem or progenitor markers and low expression of differentiation markers. Microarray analysis revealed that tumors of astrocytic and neuronal origin match the mesenchymal GBM subtype. We propose that most differentiated cells in the CNS upon defined genetic alterations undergo dedifferentiation to generate a NSC or progenitor state to initiate and maintain the tumor progression, as well as to give rise to the heterogeneous populations observed in malignant gliomas.

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