Evidence map›Paper›PMID 34268110›Full record

ArticleFrontiers in oncology2021

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

Luisina B Ripari, Emily S Norton, Raquel Bodoque-Villar, Stephanie Jeanneret, Montserrat Lara-Velazquez, Anna Carrano, Natanael Zarco, Carla A Vazquez-Ramos, Alfredo Quiñones-Hinojosa, Carlos de la Rosa-Prieto and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
  8. Glioblastoma and Methionine Addiction.International journal of molecular sciences · 2022
    Review
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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

11 authors at 6 institutions in 3 countries.

Luisina B RipariDepartment of Medical Sciences, Facultad de Medicina de Albacete, Universidad de Castilla-La Mancha, Albacete, Spain.
Emily S NortonDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Raquel Bodoque-VillarTranslational Research Unit, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain.
Stephanie JeanneretDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Montserrat Lara-VelazquezDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Anna CarranoDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Natanael ZarcoDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Carla A Vazquez-RamosDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Alfredo Quiñones-HinojosaDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Carlos de la Rosa-PrietoDepartment of Medical Sciences, Facultad de Medicina de Albacete, Universidad de Castilla-La Mancha, Albacete, Spain.
Hugo Guerrero-CázaresDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, United States.
Mayo Clinic in Florida · USWinnMed · USUniversity of Castilla-La Mancha · ESHospital General Universitario de Ciudad Real · ESJacksonville College · USUniversity of Geneva · CH

Funding

Intra-Operative, Label-Free Detection of Brain Cancer Infiltration with Quantitative Optical ImagingR01CA200399 · NCI · JOHNS HOPKINS UNIVERSITY · PI LI, XINGDE, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$3.0M
A novel microfluidic device to predict brain cancer prognosis and response to therapyR01CA216855 · NCI · MAYO CLINIC JACKSONVILLE · PI KONSTANTOPOULOS, KONSTANTINOS, QUINONES-HINOJOSA, ALFREDO · 2018 to 2022
$2.4M
Nanoparticle Modified Human Fat Derived Mesenchymal Stem Cells for Brain Cancer (Change of Organization Application)R01CA195503 · NCI · MAYO CLINIC JACKSONVILLE · PI GREEN, JORDAN, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$1.9M
BMP4 Engineered Mesenchymal Stem Cell Therapy for GlioblastomaR01CA183827 · NCI · MAYO CLINIC JACKSONVILLE · PI QUINONES-HINOJOSA, ALFREDO · 2015 to 2019
$1.9M
Chemically produced neural progenitors as a delivery vehicle for anti-glioma therapyR43CA221490 · NCI · CELL REPROGRAMMING AND THERAPEUTICS, LLC · PI ALEXANIAN, ARSHAK R, QUINONES-HINOJOSA, ALFREDO · 2018 to 2018
$300k
Role of SerpinA3 in the response of glioblastoma to cerebrospinal fluidR03NS109444 · NINDS · MAYO CLINIC JACKSONVILLE · PI GUERRERO-CAZARES, HUGO · 2018 to 2019
$236k
NCI NIH HHS R01 CA183827NCI NIH HHS R01 CA195503NCI NIH HHS R01 CA200399NCI NIH HHS R01 CA216855NCI NIH HHS R43 CA221490NINDS NIH HHS R03 NS109444
6 · The paper itself

Abstract

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.

Indexed as

cancer stem cell (CSC)glioblastomalateral ventricleneural stem cell (NSC)neurogenic nichesubventricular zone (SVZ)

Identifiers

PMID34268110
PMCPMC8277421
OpenAlexW3174868260

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.