Evidence map›Paper›PMID 21999225›Full record

ArticleCurrent eye research2011

Semaphorin 7A promotes angiogenesis in an experimental corneal neovascularization model.

Ramon C Ghanem, Kyu Yeon Han, Juan Rojas, Okan Ozturk, David J Kim, Sandeep Jain, Jin-Hong Chang, Dimitri T Azar

Open access · greenAbstract readComparative Study
In one paragraph

Article in Current eye research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The role of the semaphorins in cancer.Cell adhesion & migration · 2016
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Semaphorin 7a links nerve regeneration and inflammation in the cornea.Investigative ophthalmology & visual science · 2012
    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 1 institution in 1 country.

Ramon C GhanemDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, USA.
Kyu Yeon Han
Juan Rojas
Okan Ozturk
David J Kim
Sandeep Jain
Jin-Hong Chang
Dimitri T Azar
University of Illinois Chicago · US

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MCANANY, JAMES JASON · 1985 to 2025
$14.8M
METALLOPROTEINASE EXPRESSION IN CORNEAL WOUNDSR01EY010101 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI AZAR, DIMITRI T · 1999 to 2020
$6.5M
Inhibition of VEGF receptor dimerization and signaling in corneal lymphangiogenesR21EY021886 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHANG, JIN-HONG · 2011 to 2012
$438k
METALLOPROTEINASE EXPRESSION IN CORNEAL WOUNDSR29EY010101 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI AZAR, DIMITRI T. · 1994 to 1998
–
NEI NIH HHS EY001792NEI NIH HHS EY10101NEI NIH HHS P30 EY001792NEI NIH HHS R01 EY010101NEI NIH HHS R21 EY021886
6 · The paper itself

Abstract

purposeTo characterize the involvement of Semaphorin 7A (Sema7a) in corneal neovascularization (NV).

methodsWe generated anti-Sema7A antibodies to detect protein expression in corneal fibroblasts. Corneal fibroblast cells were cultured, stimulated with basic fibroblast growth factor (bFGF or FGF-2), immunostained with anti-Sema7A antibodies, and visualized by confocal microscopy. bFGF pellets were implanted in mouse corneal micropockets for 3-10 days, and corneal sections were immunostained with anti-Sema7A antibodies. Mouse corneas were injected with a Sema7A expression vector or a control vector for 3, 7, and 10 days. Mouse corneas were imaged by slit lamp microscopy, and areas of corneal NV were calculated using the ImageJ program. Mouse corneal sections were also immunostained with anti-macrophage marker (F4/80) and anti-vascular endothelial growth factor (VEGF)-A antibodies.

resultsOur data showed enhanced Sema7A expression levels in bFGF-stimulated cultured corneal fibroblasts. bFGF corneal implantation also demonstrated enhanced Sema7A expression. Corneas injected with a Sema7A expression vector showed evidence of significant corneal NV compared to controls on day 10 (1.8 mm(2) vs. 0.11 mm(2); p < 0.02). Additionally, immunolocalization of Sema7A expression vector-injected corneas (at day 7) revealed macrophage recruitment and enhanced VEGF-A levels.

conclusionsWe demonstrated that Sema7A was expressed in vascularized corneas and showed pro-angiogenic properties in our corneal model. Understanding the mechanism of Sema7A in angiogenesis may provide a therapeutic target for the treatment of corneal angiogenesis-related disorders.

Indexed as

Gene Expression RegulationAnimalsAntigens, CDCells, CulturedCorneal NeovascularizationDisease Models, AnimalDNA, ComplementaryFemaleFibroblastsMaleMiceMice, Inbred C57BLMicroscopy, ConfocalNeovascularization, PhysiologicSemaphorinsAntigens, CDDNA, ComplementarySema7a protein, mouseSemaphorins

Identifiers

PMID21999225
PMCPMC3709026
OpenAlexW2075263517

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.