Evidence map›Paper›PMID 18684337›Full record

ReviewExpert reviews in molecular medicine2008

New molecular targets in angiogenic vessels of glioblastoma tumours.

Joshua C Anderson, Braden C McFarland, Candece L Gladson

Open access · greenAbstract readReview
In one paragraph

Review in Expert reviews in molecular medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 72 citations in OpenAlex.

  1. Trial
  2. Impact of hypoxia on the molecular content of glioblastoma-derived exosomes.Extracellular vesicles and circulating nucleic acids · 2024
    Review
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  16. VEGF and TSP1 levels correlate with prognosis in advanced non-small cell lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2013
    Article
  17. Article
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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

3 authors at 1 institution in 1 country.

Joshua C AndersonDepartment of Pathology, Division of Neuropathology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Braden C McFarland
Candece L Gladson
University of Alabama at Birmingham · US

Funding

Training Program in Brain Tumor BiologyT32NS048039 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BENVENISTE, ETTY N · 2007 to 2017
$2.0M
The Role of TSP-1 and 2 in the Biology of AstrocytomasR01CA097110 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GLADSON, CANDECE L. · 2002 to 2006
$1.4M
Inhibition of Glioma Growth by a Novel MoleculeR01CA127620 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GLADSON, CANDECE L · 2007 to 2011
$1.4M
The Role of Lyn in Glioma Progression and MigrationR01CA109748 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GLADSON, CANDECE L · 2005 to 2009
$1.4M
NCI NIH HHS CA109748NCI NIH HHS CA127620NCI NIH HHS R01 CA097110NINDS NIH HHS T32 NS048039
6 · The paper itself

Abstract

Antiangiogenesis approaches have the potential to be particularly effective in the treatment of glioblastoma tumours. These tumours exhibit extremely high levels of neovascularisation, which may contribute to their extremely aggressive behaviour, not only by providing oxygenation and nutrition, but also by establishing a leaky vasculature that lacks a blood-brain barrier. This leaky vasculature enables migration of tumour cells, as well as the build up of fluid, which exacerbates tissue damage due to increased intracranial pressure. Here, we discuss the considerable progress that has been made in the identification of the pro- and antiangiogenic factors produced by glioblastoma tumours and the effects of these molecules in animal models of the disease. The safety and efficacy of some of these approaches have now been demonstrated in clinical trials. However, the ability of tumours to overcome these therapies and to re-establish angiogenesis requires further clinical research regarding potential multimodality therapies, as well as basic research into the regulation of angiogenesis by as yet unidentified factors. Optimisation of noninvasive procedures for monitoring of angiogenesis would greatly facilitate such research.

Indexed as

Angiogenesis Inducing AgentsAngiogenesis InhibitorsAngiogenic ProteinsAnimalsBlood-Brain BarrierBrainBrain NeoplasmsClinical Trials as TopicGlioblastomaHumansMiceNeovascularization, PathologicRatsAngiogenesis Inducing AgentsAngiogenesis InhibitorsAngiogenic Proteins

Identifiers

PMID18684337
PMCPMC2646508
OpenAlexW2165674359

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.