Evidence map›Paper›PMID 20232317›Full record

ArticleJournal of cellular physiology2010

Prolonged blockade of VEGF receptors does not damage retinal photoreceptors or ganglion cells.

Akiko Miki, Katsuaki Miki, Shinji Ueno, Delphine M Bonnet Wersinger, Cynthia Berlinicke, Gillian C Shaw, Shinichi Usui, Yuxia Wang, Donald J Zack, Peter A Campochiaro

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact, top 89% 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

29 citing papers in PubMed, 1 citations in OpenAlex.

  1. Lentiviral delivered aflibercept OXB-203 for treatment of neovascular AMD.Molecular therapy. Methods & clinical development · 2023
    Article
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  5. Article
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  7. Low risk to retina from sustained suppression of VEGF.The Journal of clinical investigation · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. AAV8-antiVEGFfab Ocular Gene Transfer for Neovascular Age-Related Macular Degeneration.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  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

10 authors at 1 institution in 1 country.

Akiko MikiDepartment of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-9277, USA.
Katsuaki Miki
Shinji Ueno
Delphine M Bonnet Wersinger
Cynthia Berlinicke
Gillian C Shaw
Shinichi Usui
Yuxia Wang
Donald J Zack
Peter A Campochiaro
Johns Hopkins University · US

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Ji Yi · 1985 to 2026
$22.1M
REGULATION OF RHODOPSIN GENE EXPRESSIONR01EY009769 · NEI · JOHNS HOPKINS UNIVERSITY · PI ZACK, DONALD J. · 1992 to 2014
$8.1M
Targeting survival factors for ocular neovascularizationR01EY012609 · NEI · JOHNS HOPKINS UNIVERSITY · PI CAMPOCHIARO, PETER A · 1999 to 2015
$5.3M
NEI NIH HHS EY009769NEI NIH HHS EY12609NEI NIH HHS P30 EY001765NEI NIH HHS P30EY1765NEI NIH HHS R01 EY009769NEI NIH HHS R01 EY012609
6 · The paper itself

Abstract

It has recently been reported that relatively short-term inhibition of vascular endothelial growth factor (VEGF) signaling can cause photoreceptor cell death, a potentially clinically important finding since VEGF blockade has become an important modality of treatment of ocular neovascularization and macular edema. However, in a set of studies in which we achieved extended and complete blockage of VEGF-induced vascular leakage through retinal expression of a VEGF binding protein, we did not observe any toxicity to retinal neurons. To follow-up on these apparently discrepant findings, we designed a set of experiments with the kinase inhibitor SU4312, which blocks phosphorylation of VEGF receptors, to look directly for evidence of VEGF inhibition-related retinal toxicity. Using transgenic mice with sustained expression of VEGF in photoreceptors, we determined that periocular injection of 3 microg of SU4312 every 5 days markedly suppressed subretinal neovascularization, indicating effective blockade of VEGF signaling. Wild-type mice given periocular injections of 5 microg of SU4312 every 5 days for up to 12 weeks showed normal scotopic and photopic electroretinograms (ERGs), no TUNEL stained cells in the retina, and no reduction in outer nuclear layer thickness. Incubation of cultured ganglion cells or retinal cultures containing photoreceptors with high doses of SU4312 did not reduce cell viability. These data suggest that blocking VEGF signaling in the retina for up to 12 weeks does not damage photoreceptors nor alter ERG function and should reassure patients who are receiving frequent injections of VEGF antagonists for choroidal and retinal vascular diseases.

Indexed as

Angiogenesis InhibitorsAnimalsCells, CulturedCell SurvivalDose-Response Relationship, DrugElectroretinographyIndolesInjectionsMiceMice, Inbred C57BLMice, TransgenicPhosphorylationPhotoreceptor Cells, VertebrateProtein Kinase InhibitorsProto-Oncogene Proteins c-aktRats3-(4-dimethylaminobenzylidene)-1,3-dihydroindol-2-oneAngiogenesis InhibitorsIndolesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor A

Identifiers

PMID20232317
PMCPMC4005719
OpenAlexW1503705025

What OpenQuestion holds

Textmetadata
LicenceTDM
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.