Evidence map›Paper›PMID 31936463›Full record

ArticleInternational journal of molecular sciences2020

Oral Delivery of a Tetrameric Tripeptide Inhibitor of VEGFR1 Suppresses Pathological Choroid Neovascularization.

Valeria Tarallo, Emanuela Iaccarino, Valeria Cicatiello, Riccardo Sanna, Menotti Ruvo, Sandro De Falco

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Observational
  6. VEGFR1 signaling in retinal angiogenesis and microinflammation.Progress in retinal and eye research · 2021
    Review
  7. Article
  8. Peptides for Health Benefits 2019.International journal of molecular sciences · 2020
    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

6 authors at 2 institutions in 1 country.

Valeria TaralloIstituto di Genetica e Biofisica 'Adriano Buzzati-Traverso'-CNR, 80131 Napoli, Italy.
Emanuela IaccarinoIstituto di Biostrutture e Bioimmagini-CNR, 80134 Napoli, Italy.
Valeria CicatielloIstituto di Genetica e Biofisica 'Adriano Buzzati-Traverso'-CNR, 80131 Napoli, Italy.
Riccardo SannaBIOVIIIx s.r.l., Department of R&D, 80142 Napoli, Italy.
Menotti RuvoIstituto di Biostrutture e Bioimmagini-CNR, 80134 Napoli, Italy.
Sandro De FalcoIstituto di Genetica e Biofisica 'Adriano Buzzati-Traverso'-CNR, 80131 Napoli, Italy.ORCID 0000-0002-6501-1697
Institute of Genetics and Biophysics · ITInstitute of Biostructure and Bioimaging · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca PRIN 2017XJ38A4Regione Campania Campania OncotherapiesRegione Campania Project SATIN - POR Campania FESR 2014/2020
6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is the primary cause of blindness in advanced countries. Repeated intravitreal delivery of anti-vascular endothelial growth factor (VEGF) agents has represented an important advancement for the therapy of wet AMD with significative results in terms of blindness prevention and partial vision restore. Nonetheless, some patients are not responsive or do not attain significant visual improvement, intravitreal injection may cause serious complications and important side effects have been reported for the prolonged block of VEGF-A. In order to evaluate new anti-angiogenic strategies, we focused our attention on VEGF receptor 1 (VEGFR1) developing a specific VEGFR-1 antagonist, a tetrameric tripeptide named inhibitor of VEGFR 1 (iVR1). We have evaluated its anti-angiogenic activity in the preclinical model of AMD, the laser-induced choroid neovascularization (CNV). iVR1 is able to potently inhibit CNV when delivered by intravitreal injection. Surprisingly, it is able to significantly reduce CNV also when delivered by gavage. Our data show that the specific block of VEGFR1 in vivo represents a valid alternative to the block of VEGF-A and that the inhibition of the pathological neovascularization at ocular level is also possible by systemic delivery of compounds not targeting VEGF-A.

Indexed as

Administration, OralAnimalsChoroidal NeovascularizationIntravitreal InjectionsLasersMice, Inbred C57BLOligopeptidesSpectroscopy, Fourier Transform InfraredTrifluoroacetic AcidVascular Endothelial Growth Factor Receptor-1OligopeptidesTrifluoroacetic AcidVascular Endothelial Growth Factor Receptor-1AMDCNVmultimeric peptidesoral deliveryVEGFR1

Identifiers

PMID31936463
PMCPMC7014271
OpenAlexW2999720436

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.