Evidence map›Paper›PMID 26578958›Full record

ArticleFrontiers in pharmacology2015

Molecular features of interaction between VEGFA and anti-angiogenic drugs used in retinal diseases: a computational approach.

Chiara B M Platania, Luisa Di Paola, Gian M Leggio, Giovanni L Romano, Filippo Drago, Salvatore Salomone, Claudio Bucolo

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 54 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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

54 citing papers in PubMed, 2 syntheses or guidelines pooled it, 83 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Efficacy and Safety of Biosimilar Ranibizumab (OPTIMABClinical ophthalmology (Auckland, N.Z.) · 2024
    Trial
  4. Article
  5. Mathematical Models of Topically and Intravitreally Applied Ranibizumab.Investigative ophthalmology & visual science · 2025
    Article
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  8. Review
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  13. Non-immediate drug hypersensitivity reactions secondary to intravitreal anti-vascular endothelial growth factors.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2022
    Article
  14. Article
  15. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Chiara B M PlataniaSection of Pharmacology, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania Catania, Italy.
Luisa Di PaolaSchool of Engineering, University Campus BioMedico Roma, Italy.
Gian M LeggioSection of Pharmacology, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania Catania, Italy.
Giovanni L RomanoSection of Pharmacology, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania Catania, Italy.
Filippo DragoSection of Pharmacology, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania Catania, Italy.
Salvatore SalomoneSection of Pharmacology, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania Catania, Italy.
Claudio BucoloSection of Pharmacology, Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania Catania, Italy.
University of Catania · ITUniversità Campus Bio-Medico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-angiogenic agents are biological drugs used for treatment of retinal neovascular degenerative diseases. In this study, we aimed at in silico analysis of interaction of vascular endothelial growth factor A (VEGFA), the main mediator of angiogenesis, with binding domains of anti-angiogenic agents used for treatment of retinal diseases, such as ranibizumab, bevacizumab and aflibercept. The analysis of anti-VEGF/VEGFA complexes was carried out by means of protein-protein docking and molecular dynamics (MD) coupled to molecular mechanics-Poisson Boltzmann Surface Area (MM-PBSA) calculation. Molecular dynamics simulation was further analyzed by protein contact networks. Rough energetic evaluation with protein-protein docking scores revealed that aflibercept/VEGFA complex was characterized by electrostatic stabilization, whereas ranibizumab and bevacizumab complexes were stabilized by Van der Waals (VdW) energy term; these results were confirmed by MM-PBSA. Comparison of MM-PBSA predicted energy terms with experimental binding parameters reported in literature indicated that the high association rate (Kon) of aflibercept to VEGFA was consistent with high stabilizing electrostatic energy. On the other hand, the relatively low experimental dissociation rate (Koff) of ranibizumab may be attributed to lower conformational fluctuations of the ranibizumab/VEGFA complex, higher number of contacts and hydrogen bonds in comparison to bevacizumab and aflibercept. Thus, the anti-angiogenic agents have been found to be considerably different both in terms of molecular interactions and stabilizing energy. Characterization of such features can improve the design of novel biological drugs potentially useful in clinical practice.

Indexed as

afliberceptbevacizumabdiabetic retinopathymolecular dynamicsranibizumab

Identifiers

PMID26578958
PMCPMC4624855
OpenAlexW1887310754

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.