Evidence map›Paper›PMID 33638562›Full record

ReviewGlia2021

Leveraging the replication-competent avian-like sarcoma virus/tumor virus receptor-A system for modeling human gliomas.

Pranjali P Kanvinde, Adarsha P Malla, Nina P Connolly, Frank Szulzewsky, Pavlos Anastasiadis, Heather M Ames, Anthony J Kim, Jeffrey A Winkles, Eric C Holland, Graeme F Woodworth

Open access · greenAbstract readReview
In one paragraph

Review in Glia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. A systems approach identifies MERTK as a therapeutic vulnerability in ZFTA-RELA-driven ependymomas.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. A clinically relevant model and method to study necrosis as a driving force in glioma restructuring and progression.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
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

10 authors at 2 institutions in 1 country.

Pranjali P KanvindeDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0001-7906-4979
Adarsha P MallaDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Nina P ConnollyDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Frank SzulzewskyHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Pavlos AnastasiadisDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-0230-7925
Heather M AmesMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Anthony J KimDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Jeffrey A WinklesDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-3305-1424
Eric C HollandHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Graeme F WoodworthDepartment of Neurosurgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0001-9663-0768
University of Maryland, Baltimore · USFred Hutch Cancer Center · US

Funding

UNIVERSITY OF MARYLAND GREENEBAUM CANCER CENTERSUPPORT GRANTP30CA134274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FEYRUZ VIRGILIA RASSOOL · 2008 to 2026
$51.0M
Project 3: Single Cell Measures of Intratumor Diversity for Optimal Breast Cancer TherapyU54CA193461 · NCI · DANA-FARBER CANCER INST · PI POLYAK, KORNELIA · 2015 to 2020
$11.2M
Training Grant in Cancer BiologyT32CA154274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Toni M Antalis, CURT I CIVIN · 2011 to 2026
$6.8M
Mechanisms and models of C11or95 and C11or95-RELA fusions (RELAFus )U54CA243125 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HOLLAND, ERIC C. · 2019 to 2022
$6.2M
Nanotherapeutic treatment of the invasive glioblastoma microenvironmentR01NS107813 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI WOODWORTH, GRAEME F · 2019 to 2023
$2.0M
Brain-Penetrating Nanoparticle Therapeutics for Invasive Brain CancerK08NS090430 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI WOODWORTH, GRAEME F · 2014 to 2018
$748k
NCI NIH HHS P30 CA134274NCI NIH HHS T32 CA154274NCI NIH HHS U54 CA193461NCI NIH HHS U54 CA243125NINDS NIH HHS K08 NS090430NINDS NIH HHS R01 NS107813
6 · The paper itself

Abstract

Gliomas are the most common primary intrinsic brain tumors occurring in adults. Of all malignant gliomas, glioblastoma (GBM) is considered the deadliest tumor type due to diffuse brain invasion, immune evasion, cellular, and molecular heterogeneity, and resistance to treatments resulting in high rates of recurrence. An extensive understanding of the genomic and microenvironmental landscape of gliomas gathered over the past decade has renewed interest in pursuing novel therapeutics, including immune checkpoint inhibitors, glioma-associated macrophage/microglia (GAMs) modulators, and others. In light of this, predictive animal models that closely recreate the conditions and findings found in human gliomas will serve an increasingly important role in identifying new, effective therapeutic strategies. Although numerous syngeneic, xenograft, and transgenic rodent models have been developed, few include the full complement of pathobiological features found in human tumors, and therefore few accurately predict bench-to-bedside success. This review provides an update on how genetically engineered rodent models based on the replication-competent avian-like sarcoma (RCAS) virus/tumor virus receptor-A (tv-a) system have been used to recapitulate key elements of human gliomas in an immunologically intact host microenvironment and highlights new approaches using this model system as a predictive tool for advancing translational glioma research.

Indexed as

Brain NeoplasmsDisease Models, AnimalGliomaSarcomaAnimalsAvian Sarcoma VirusesHumansOncogenic VirusesReceptors, VirusTumor MicroenvironmentReceptors, Virusanimal modelinggenetically engineeredglioblastomahigh-grade gliomaimmunocompetentpatient-derived xenograftpreclinical testingRCAS/tv-atumor microenvironment

Identifiers

PMID33638562
PMCPMC8591561
OpenAlexW3132577484

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.