Evidence map›Paper›PMID 23047550›Full record

ArticleBritish journal of cancer2012

Vascular endothelial growth factor signals through platelet-derived growth factor receptor β in meningiomas in vitro.

C Pfister, H Pfrommer, M S Tatagiba, F Roser

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Roles of PDGF/PDGFR signaling in various organs.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. UnderstandingCells · 2023
    Article
  7. Article
  8. Extracellular Vesicles and Hypertension.Advances in experimental medicine and biology · 2023
    Article
  9. Article
  10. Article
  11. Molecular neuropathology of brain-invasive meningiomas.Brain pathology (Zurich, Switzerland) · 2022
    Review
  12. Review
  13. Gambogic acid: A shining natural compound to nanomedicine for cancer therapeutics.Biochimica et biophysica acta. Reviews on cancer · 2020
    Review
  14. Article
  15. mRNA expression of tumor-associated genes in canine grade I meningiomas.The Journal of veterinary medical science · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. An unusual complex karyotype in myopericytoma.Journal of orthopaedics · 2015
    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

4 authors at 1 institution in 1 country.

C PfisterDepartment of Neurosurgery, University of Tuebingen, Hoppe-Seyler-Strasse 3, Tuebingen 72076, Germany. christina.pfister@med.uni-tuebingen.de
H Pfrommer
M S Tatagiba
F Roser
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVascular endothelial growth factor (VEGF)-mediated angiogenesis mediates tumour growth and metastasis. Meningiomas are primarily benign, slow-growing, highly vascularised tumours. Aside from VEGF, there is little data on the function of major angiogenic proteins in meningiomas.

methodsThe VEGFA, platelet-derived growth factor B (PDGFB), and their respective receptors - VEGF receptor 2 (KDR) and PDGF receptor β (PDGFRβ) - were quantified using real-time PCR and a TaqMan Protein Assay in meningiomas in vivo and in vitro. The effect of VEGFA and PDGFB on cell proliferation and the tyrosine phosphorylation of PDGFRβ were examined.

resultsMost meningiomas displayed no KDR protein expression but elevated PDGFRβ levels. Exogenous VEGFA stimulation significantly increased cell proliferation. The PDGFRβ inhibition before stimulation with VEGFA abolished the proliferative stimuli. The VEGFA induced concentration-dependent PDGFRβ tyrosine phosphorylation comparable to PDGFB-induced PDGFRβ tyrosine phosphorylation. The PDGFRβ inhibitors gambogic acid, sunitinib, and tandutinib equally impaired the migration of meningioma cells. In addition, gambogic acid suppressed the VEGFA-induced PDGFRβ tyrosine phosphorylation.

conclusionCollectively, our data suggest that VEGFA primarily regulates VEGF-mediated migration through PDGFRβ in meningiomas. The inhibitory effect of gambogic acid and tandutinib against meningioma growth in vitro suggests that selective PDGFRβ inhibitors, in combination with VEGF inhibitors, should be evaluated further as potential therapies for recurrent and malignant meningiomas.

Indexed as

Angiogenic ProteinsCell ProliferationHumansIndolesMeningeal NeoplasmsMeningiomaNeovascularization, PathologicPhosphorylationPiperazinesProto-Oncogene Proteins c-sisPyrrolesQuinazolinesReceptor, Platelet-Derived Growth Factor betaReceptors, Vascular Endothelial Growth FactorSignal TransductionSunitinibAngiogenic Proteinsgambogic acidIndolesPiperazinesProto-Oncogene Proteins c-sisPyrrolesQuinazolinesReceptor, Platelet-Derived Growth Factor betaReceptors, Vascular Endothelial Growth FactorSunitinibtandutinibTyrosineVascular Endothelial Growth Factor AVEGFA protein, humanXanthones

Identifiers

PMID23047550
PMCPMC3493872
OpenAlexW2002015428

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.