4.6 Article

Glioblastoma Proximity to the Lateral Ventricle Alters Neurogenic Cell Populations of the Subventricular Zone

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FRONTIERS IN ONCOLOGY
卷 11, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2021.650316

关键词

glioblastoma; subventricular zone (SVZ); lateral ventricle; neural stem cell (NSC); cancer stem cell (CSC); neurogenic niche

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资金

  1. Mayo Clinic Graduate School of Biomedical Sciences
  2. Mayo Clinic Center for Regenerative Medicine
  3. Uihlein Professorship Research Grant
  4. CONACYT, UNAM
  5. Mayo Clinic Professorship
  6. Clinician Investigator grant
  7. National Institutes of Health (NIH) [R43CA221490, R01CA200399, R01CA183827, R01CA195503, R01CA216855]
  8. NIH [R03NS109444, R21CA221490, K01NS11093001]

向作者/读者索取更多资源

A novel rodent model was used to analyze the bidirectional signaling between GBM tumors and cells within the subventricular zone (SVZ). The study found that GBM tumors located close to the lateral ventricles show increased tumor growth, decreased median survival, and negatively influence the neurogenic and cell division process of the SVZ in adult mice. This model will be invaluable for further investigation into the interactions between GBM and the neurogenic cell populations of the SVZ.
Despite current strategies combining surgery, radiation, and chemotherapy, glioblastoma (GBM) is the most common and aggressive malignant primary brain tumor in adults. Tumor location plays a key role in the prognosis of patients, with GBM tumors located in close proximity to the lateral ventricles (LVs) resulting in worse survival expectancy and higher incidence of distal recurrence. Though the reason for worse prognosis in these patients remains unknown, it may be due to proximity to the subventricular zone (SVZ) neurogenic niche contained within the lateral wall of the LVs. We present a novel rodent model to analyze the bidirectional signaling between GBM tumors and cells contained within the SVZ. Patient-derived GBM cells expressing GFP and luciferase were engrafted at locations proximal, intermediate, and distal to the LVs in immunosuppressed mice. Mice were either sacrificed after 4 weeks for immunohistochemical analysis of the tumor and SVZ or maintained for survival analysis. Analysis of the GFP+ tumor bulk revealed that GBM tumors proximal to the LV show increased levels of proliferation and tumor growth than LV-distal counterparts and is accompanied by decreased median survival. Conversely, numbers of innate proliferative cells, neural stem cells (NSCs), migratory cells and progenitors contained within the SVZ are decreased as a result of GBM proximity to the LV. These results indicate that our rodent model is able to accurately recapitulate several of the clinical aspects of LV-associated GBM, including increased tumor growth and decreased median survival. Additionally, we have found the neurogenic and cell division process of the SVZ in these adult mice is negatively influenced according to the presence and proximity of the tumor mass. This model will be invaluable for further investigation into the bidirectional signaling between GBM and the neurogenic cell populations of the SVZ.

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