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The hypoxic peri-arteriolar glioma stem cell niche,an integrated concept of five types of niches in human glioblastoma
Authors:Diana A. Aderetti  Vashendriya V.V. Hira  Remco J. Molenaar  Cornelis J.F. van Noorden
Affiliation:1. Department of Medical Biology, Cancer Center Amsterdam at the Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands;2. Department of Medical Oncology, Cancer Center Amsterdam at the Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands;3. Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ve?na pot 111, 1000 Ljubljana, Slovenia
Abstract:Glioblastoma is the most lethal primary brain tumor and poor survival of glioblastoma patients is attributed to the presence of glioma stem cells (GSCs). These therapy-resistant, quiescent and pluripotent cells reside in GSC niches, which are specific microenvironments that protect GSCs against radiotherapy and chemotherapy. We previously showed the existence of hypoxic peri-arteriolar GSC niches in glioblastoma tumor samples. However, other studies have described peri-vascular niches, peri-hypoxic niches, peri-immune niches and extracellular matrix niches of GSCs. The aim of this review was to critically evaluate the literature on these five different types of GSC niches. In the present review, we describe that the five niche types are not distinct from one another, but should be considered to be parts of one integral GSC niche model, the hypoxic peri-arteriolar GSC niche. Moreover, hypoxic peri-arteriolar GSC niches are structural and functional look-alikes of hematopoietic stem cell (HSC) niches in the bone marrow. GSCs are maintained in peri-arteriolar niches by the same receptor-ligand interactions as HSCs in bone marrow. Our concept should be rigidly tested in the near future and applied to develop therapies to expel and keep GSCs out of their protective niches to render them more vulnerable to standard therapies.
Keywords:ALL  acute lymphoblastic leukemia  AML  acute myeloid leukemia  CatK  cathepsin K  CXCR4  C-X-C receptor type 4  DLL4  Delta-like ligand 4  GSC  glioma stem cell  EC  endothelial cell  ECM  extracellular matrix  GM-CSF  granulocyte/macrophage colony-stimulated factor  HIF  hypoxia-inducible factor  HSC  hematopoietic stem cell  HSP  hypoxia stress-induced chaperone protein  J1  Jagged-1  M-CSF  monocyte chemoattraction protein-1  MMP  matrix metalloprotease  MSC  mesenchymal stem cell  NO  nitric oxide  OPN  osteopontin  SDF-1α  stromal-derived factor-1α  SHH  Sonic Hedgehog  SCF  stem cell factor  TAM  tumor-associated macrophage  TGF-β  transforming growth factor-β  VEGF  vascular endothelial growth factor  VCAM-1  vascular cell adhesion molecule-1  Glioblastoma  Glioma stem cells  Niches  Blood vessels  Extracellular matrix  Tumor microenvironment  Hypoxia  Therapy resistance  Vasculature
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