4.5 Review

The cellular origin for malignant glioma and prospects for clinical advancements

Journal

EXPERT REVIEW OF MOLECULAR DIAGNOSTICS
Volume 12, Issue 4, Pages 383-394

Publisher

TAYLOR & FRANCIS AS
DOI: 10.1586/ERM.12.30

Keywords

animal model; astrocyte; cell of mutation; cell of origin; cell-targeted therapy; malignant glioma; molecular pathology; neural stem cell; oligodendrocyte progenitor cell; tumor subtype

Categories

Funding

  1. National Cancer Institute (NIH/NCI) [R01CA136495, U24CA143883]
  2. WM Keck Foundation
  3. Pew Charitable Trusts
  4. National Institute of Neurological Disease (NIH/NINDS) [R01NS066955]

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Glioma remains incurable despite great advancements in medicine. Targeting the cell of origin for gliomas could bring great hope for patients. However, as a collection of diverse diseases, each subtype of glioma could derive from a distinct cell of origin. To resolve such a complex problem, one must use multiple research approaches to gain deep insights. Here we review current evidence regarding the cell of origin from clinical observations, whole-genome molecular pathology and glioma animal models. We conclude that neural stem cells, glial progenitors (including oligodendrocyte progenitor cells) and astrocytes could all serve as cells of origin for gliomas, and that cells incurring initial mutations (cells of mutation) might not transform, while their progeny cells could instead transform and act as cells of origin. Further studies with multidisciplinary approaches are needed to link each subtype to a particular cell of origin, and to develop effective therapies that target the signaling network within these cells.

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