Evidence map›Paper›PMID 16389942›Full record

ReviewBrain pathology (Zurich, Switzerland)2005

Angiogenesis in gliomas: biology and molecular pathophysiology.

Ingeborg Fischer, Jean-Pierre Gagner, Meng Law, Elizabeth W Newcomb, David Zagzag

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Brain pathology (Zurich, Switzerland), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05274919 (Vascular Signature Mapping of Brain Tumor Genotypes), which is not on this map. Cited by 167 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed, 2 pooled it
7.8field-weighted citation impact, top 2% 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.

NCT05274919 recruitingnot on this mapstarted 2022, after this paper: background citation

Vascular Signature Mapping of Brain Tumor Genotypes

Typeobservational_patient_registrySponsorLeiden University Medical CenterRan2022 to 2026Enrolled180ConditionsGliomaArmsPhilips Achieva 7T MRI, X-ray (optional), Additional contrast injection, Question list
3 · Its place in the literature

Who cites it

167 citing papers in PubMed, 2 syntheses or guidelines pooled it, 344 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Trial
  4. The prognostic value of [European journal of nuclear medicine and molecular imaging · 2018
    Trial
  5. Trial
  6. Phase II study of bevacizumab in combination with sorafenib in recurrent glioblastoma (N0776): a north central cancer treatment group trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Trial
  7. Trial
  8. Trial
  9. Observational
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

107 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Ingeborg FischerMicrovascular and Molecular Neuro-oncology Laboratory, New York University School of Medicine, USA.
Jean-Pierre Gagner
Meng Law
Elizabeth W Newcomb
David Zagzag
New York University · USUniversity School · US

Funding

Invasion and Angiogenesis in Malignant GliomasR01CA100426 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZAGZAG, DAVID · 2004 to 2008
$1.4M
NCI NIH HHS R01 CA100426
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is characterized by exuberant angiogenesis, a key event in tumor growth and progression. The pathologic mechanisms driving this change and the biological behavior of gliomas remain unclear. One mechanism may involve cooption of native blood vessels by glioma cells inducing expression of angiopoietin-2 by endothelial cells. Subsequently, vascular apoptosis and involution leads to necrosis and hypoxia. This in turn induces angiogenesis that is associated with expression of hypoxia-inducible factor (HIF)-1alpha and vascular endothelial growth factor (VEGF) in perinecrotic pseudopalisading glioma cells. Here we review the molecular and cellular mechanisms implicated in HIF-1-dependent and HIF-1-independent glioma-associated angiogenesis. In GBMs, both tumor hypoxia and genetic alterations commonly occur and act together to induce the expression of HIF-1. The angiogenic response of the tumor to HIF-1 is mediated by HIF-1-regulated target genes leading to the upregulation of several proangiogenic factors such as VEGF and other adaptive response molecules. Understanding the roles of these regulatory processes in tumor neovascularization, tumor growth and progression, and resistance to therapy will ultimately lead to the development of improved antiangiogenic therapies for GBMs.

Indexed as

AnimalsBrain NeoplasmsGliomaHumansHypoxia-Inducible Factor 1, alpha SubunitNeovascularization, PathologicVascular Endothelial Growth Factor AHypoxia-Inducible Factor 1, alpha SubunitVascular Endothelial Growth Factor A

Identifiers

PMID16389942
PMCPMC8096031
OpenAlexW2130852323

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.