Evidence map›Paper›PMID 21880113›Full record

ArticleJournal of cellular and molecular medicine2012

Angiostatic kinase inhibitors to sustain photodynamic angio-occlusion.

Patrycja Nowak-Sliwinska, Andrea Weiss, Judy R van Beijnum, Tse J Wong, Jean-Pierre Ballini, Blaise Lovisa, Hubert van den Bergh, Arjan W Griffioen

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of cellular and molecular medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-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

30 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Medication Trends for Age-Related Macular Degeneration.International journal of molecular sciences · 2021
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. A Tumor Vascular-Targeted Interlocking Trimodal Nanosystem That Induces and Exploits Hypoxia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. The role of photodynamic therapy in overcoming cancer drug resistance.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2015
    Review
  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

8 authors at 3 institutions in 3 countries.

Patrycja Nowak-SliwinskaAngiogenesis Laboratory, Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands. Patrycja.Nowak-Sliwinska@epfl.ch
Andrea Weiss
Judy R van Beijnum
Tse J Wong
Jean-Pierre Ballini
Blaise Lovisa
Hubert van den Bergh
Arjan W Griffioen
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLÉcole Polytechnique Fédérale de Lausanne · CHCentre Jean Bernard · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted angiostatic therapy receives major attention for the treatment of cancer and exudative age-related macular degeneration (AMD). Photodynamic therapy (PDT) has been used as an effective clinical approach for these diseases. As PDT can cause an angiogenic response in the treated tissue, combination of PDT with anti-angiogenic compounds should lead to improved therapy. This study was undertaken to test the clinically used small molecule kinase inhibitors Nexavar® (sorafenib), Tarceva® (erlotinib) and Sutent® (sunitinib) for this purpose, and to compare the results to the combination of Visudyne®-PDT with Avastin® (bevacizumab) treatment. When topically applied to the chicken chorioallantoic membrane at embryo development day (EDD) 7, a clear inhibition of blood vessel development was observed, with sorafenib being most efficient. To investigate the combination with phototherapy, Visudyne®-PDT was first applied on EDD11 to close all <100 μm vessels. Application of angiostatics after PDT resulted in a significant decrease in vessel regrowth in terms of reduced vessel density and number of branching points/mm(2) . As the 50% effective dose (ED50) for all compounds was approximately 10-fold lower, Sorafenib outperformed the other compounds. In vitro, all kinase inhibitors decreased the viability of human umbilical vein endothelial cells. Sunitinib convincingly inhibited the in vitro migration of endothelial cells. These results suggest the therapeutic potential of these compounds for application in combination with PDT in anti-cancer approaches, and possibly also in the treatment of other diseases where angiogenesis plays an important role.

Indexed as

Angiogenesis InhibitorsAnimalsAntibodies, Monoclonal, HumanizedBenzenesulfonatesBevacizumabCell LineCell ProliferationChick EmbryoChorioallantoic MembraneErlotinib HydrochlorideHumansHuman Umbilical Vein Endothelial CellsIndolesMicroscopy, FluorescenceNiacinamidePhenylurea CompoundsAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedBenzenesulfonatesBevacizumabErlotinib HydrochlorideIndolesNiacinamidePhenylurea CompoundsPorphyrinsProtein Kinase InhibitorsPyridinesPyrrolesQuinazolinesSorafenibSunitinibVerteporfin

Identifiers

PMID21880113
PMCPMC3823223
OpenAlexW1982267959

What OpenQuestion holds

Textmetadata
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.