Evidence map›Paper›PMID 22906922›Full record

ReviewNeuroscience letters2012

Anti-angiogenic gene therapy in the treatment of malignant gliomas.

NaTosha N Gatson, E Antonio Chiocca, Balveen Kaur

Abstract readReview
In one paragraph

Review in Neuroscience letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Oncolytic HSV and cancer drug interactions: Current clinical status and future directions.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  2. Review
  3. Circular RNAs-mediated angiogenesis in human cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Circular RNAs: Functions and Prospects in Glioma.Journal of molecular neuroscience : MN · 2019
    Review
  15. Article
  16. Combinatorial Effects of VEGFR Kinase Inhibitor Axitinib and Oncolytic Virotherapy in Mouse and Human Glioblastoma Stem-Like Cell Models.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  17. Article
  18. Article
  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

3 authors.

NaTosha N GatsonDardinger Center for Neuro-oncology and Neurosciences, N-1017 Doan Hall, 410 W. 10th Avenue, James Cancer Hospital/Solove Research Institute and The Ohio State University Wexner Medical Center, Columbus, OH 43210-1240, USA.
E Antonio Chiocca
Balveen Kaur

Funding

The role of microvesicles in giloma virotherapyP01CA069246 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BREAKEFIELD, XANDRA OWENS, CHIOCCA, E. ANTONIO · 1996 to 2021
$30.9M
Ohio State Neuroscience Centr CoreP30NS045758 · NINDS · OHIO STATE UNIVERSITY · PI MCTIGUE, DANA M · 2004 to 2015
$7.7M
Preclinical Toxicity Evaluation of a Potent Oncolytic VirusU01NS061811 · NINDS · OHIO STATE UNIVERSITY · PI CHIOCCA, E. ANTONIO · 2008 to 2012
$4.6M
Enhancing Viral Oncolysis with Vasculostatin Gene DeliveryR01CA150153 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2011 to 2020
$4.0M
OV Therapy Induced Changes in Tumor Secretome and Their Impact on TherapyR01NS064607 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2008 to 2018
$3.2M
Combination of Cliengitide and Oncolytic HSV: a toxicology study for brain tumorsK01NS059575 · NINDS · OHIO STATE UNIVERSITY · PI KAUR, BALVEEN · 2008 to 2011
$526k
Oncolytic HSV Cancer Therapy: Enhancement by Vasculostatin Gene TherapyR21NS056203 · NINDS · OHIO STATE UNIVERSITY · PI KAUR, BALVEEN · 2007 to 2008
$361k
Research Education Program for Residents/Fellows in Neurology and NeurosurgeryR25NS065734 · NINDS · OHIO STATE UNIVERSITY · PI LONSER, RUSSELL · 2009 to 2014
$247k
NCI NIH HHS P01 CA069246NCI NIH HHS R01 CA150153NINDS NIH HHS K01 NS059575NINDS NIH HHS P30 NS045758NINDS NIH HHS R01 NS064607NINDS NIH HHS R21 NS056203NINDS NIH HHS R25 NS065734NINDS NIH HHS U01 NS061811
6 · The paper itself

Abstract

More than four decades ago, Dr. Judah Folkman hypothesized that angiogenesis was a critical process in tumor growth. Since that time, there have been significant advances in understanding tumor biology and groundbreaking research in cancer therapy that have validated his hypothesis. However, in spite of extensive research, glioblastoma multiforme (GBM), the most common and malignant primary brain tumor, has gained little in the way of improved median survival. There have been several angiogenesis targets that have resulted in drugs that are in clinical trials or FDA approved for clinical use in several cancers. GBM is a highly angiogenic tumor and several drugs are showing promise in clinical trials with one (bevacizumab), clinically approved for use. We will review several possible angiogenic targets in GBM as well as the vector methodologies used for delivery. In addition, GBMs present several therapeutic challenges related to structure, tumor immune microenvironment and resistance to angiogenesis. To overcome these challenges will require novel approaches to improve therapeutic gene expression and vector biodistribution in the glioma.

Indexed as

Genetic TherapyBrain NeoplasmsGenetic VectorsGlioblastomaHumansNeovascularization, PathologicTumor Microenvironment

Identifiers

PMID22906922
PMCPMC3471371

What OpenQuestion holds

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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.