Evidence map›Paper›PMID 26720197›Full record

ArticlePloS one2015

Robo 4 Counteracts Angiogenesis in Herpetic Stromal Keratitis.

Fernanda Gimenez, Sachin Mulik, Tamara Veiga-Parga, Siddheshvar Bhela, Barry T Rouse

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Clinical Management of Herpes Simplex Virus Keratitis.Diagnostics (Basel, Switzerland) · 2022
    Review
  4. Article
  5. Review
  6. The endothelial tip-stalk cell selection and shuffling during angiogenesis.Journal of cell communication and signaling · 2019
    Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Challenges of corneal infections.Expert review of ophthalmology · 2016
    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

5 authors at 1 institution in 1 country.

Fernanda GimenezDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996, United States of America.
Sachin MulikDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996, United States of America.
Tamara Veiga-PargaDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996, United States of America.
Siddheshvar BhelaDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996, United States of America.
Barry T RouseDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996, United States of America.
University of Tennessee at Knoxville · US

Funding

NEI NIH HHS EY 005093NIAID NIH HHS AI 06335
6 · The paper itself

Abstract

The cornea is a complex tissue that must preserve its transparency to maintain optimal vision. However, in some circumstances, damage to the eye can result in neovascularization that impairs vision. This outcome can occur when herpes simplex virus type 1 (HSV-1) causes the immunoinflammatory lesion stromal keratitis (SK). Potentially useful measures to control the severity of SK are to target angiogenesis which with herpetic SK invariably involves VEGF. One such way to control angiogenesis involves the endothelial receptor Robo4 (R4), which upon interaction with another protein activates an antiangiogenic pathway that counteracts VEGF downstream signaling. In this study we show that mice unable to produce R4 because of gene knockout developed significantly higher angiogenesis after HSV-1 ocular infection than did infected wild type (WT) controls. Moreover, providing additional soluble R4 (sR4) protein by subconjunctival administration to R4 KO HSV-1 infected mice substantially rescued the WT phenotype. Finally, administration of sR4 to WT HSV-1 infected mice diminished the extent of corneal angiogenesis compared to WT control animals. Our results indicate that sR4 could represent a useful therapeutic tool to counteract corneal angiogenesis and help control the severity of SK.

Indexed as

AnimalsCorneal NeovascularizationDisease Models, AnimalFemaleGenetic Predisposition to DiseaseHerpesvirus 1, HumanKeratitis, HerpeticMiceMice, KnockoutNeovascularization, PathologicNerve Tissue ProteinsPhenotypeReceptors, Cell SurfaceReceptors, ImmunologicSignal TransductionVascular Endothelial Growth Factor ANerve Tissue ProteinsReceptors, Cell SurfaceReceptors, ImmunologicRobo4 protein, mouseVascular Endothelial Growth Factor A

Identifiers

PMID26720197
PMCPMC4697792
OpenAlexW2205259920

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.