Evidence map›Paper›PMID 35359410›Full record

ReviewFrontiers in oncology2022

The Subventricular Zone in Glioblastoma: Genesis, Maintenance, and Modeling.

Jamison Beiriger, Ahmed Habib, Nicolina Jovanovich, Chowdari V Kodavali, Lincoln Edwards, Nduka Amankulor, Pascal O Zinn

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. In Vivo Evaluation ofPharmaceutics · 2024
    Article
  10. Review
  11. Gene Expression of GABABrain sciences · 2024
    Article
  12. Glioblastoma Therapy: Past, Present and Future.International journal of molecular sciences · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jamison BeirigerDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Ahmed HabibDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Nicolina JovanovichDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Chowdari V KodavaliDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Lincoln EdwardsDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Nduka AmankulorDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Pascal O ZinnDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
University of Pittsburgh Medical Center · USUPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
NCI NIH HHS P30 CA047904
6 · The paper itself

Abstract

Glioblastoma (GBM) is a malignant tumor with a median survival rate of 15-16 months with standard care; however, cases of successful treatment offer hope that an enhanced understanding of the pathology will improve the prognosis. The cell of origin in GBM remains controversial. Recent evidence has implicated stem cells as cells of origin in many cancers. Neural stem/precursor cells (NSCs) are being evaluated as potential initiators of GBM tumorigenesis. The NSCs in the subventricular zone (SVZ) have demonstrated similar molecular profiles and share several distinctive characteristics to proliferative glioblastoma stem cells (GSCs) in GBM. Genomic and proteomic studies comparing the SVZ and GBM support the hypothesis that the tumor cells and SVZ cells are related. Animal models corroborate this connection, demonstrating migratory patterns from the SVZ to the tumor. Along with laboratory and animal research, clinical studies have demonstrated improved progression-free survival in patients with GBM after radiation to the ipsilateral SVZ. Additionally, key genetic mutations in GBM for the most part carry regulatory roles in the SVZ as well. An exciting avenue towards SVZ modeling and determining its role in gliomagenesis in the human context is human brain organoids. Here we comprehensively discuss and review the role of the SVZ in GBM genesis, maintenance, and modeling.

Indexed as

glioblastomamodelingorganoidSVZventricular

Identifiers

PMID35359410
PMCPMC8960165
OpenAlexW4221086781

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.