Evidence map›Paper›PMID 28777835›Full record

ArticleInvestigative ophthalmology & visual science2017

Effect of Methotrexate on an In Vitro Patient-Derived Model of Proliferative Vitreoretinopathy.

Dhanesh Amarnani, Arturo Israel Machuca-Parra, Lindsay L Wong, Christina K Marko, James A Stefater, Tomasz P Stryjewski, Dean Eliott, Joseph F Arboleda-Velasquez, Leo A Kim

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06038968 (Anatomical and Functional Outcomes of Use of Methotrexate Infusion and Intrasilicone Injection During Diabetic Vitrectomy), which is not on this map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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.

NCT06038968 early_phase1completednot on this mapstarted 2022, after this paper: background citation

Anatomical and Functional Outcomes of Use of Methotrexate Infusion and Intrasilicone Injection During Diabetic Vitrectomy

TypeinterventionalSponsorMinia UniversityRan2022 to 2024Enrolled60ConditionsDiabetic Retinopathy, Vitreomacular TractionArmsMethotrexate 25 MG/ML, parsplana vitrectomy
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Fibrotic Changes in Rhegmatogenous Retinal Detachment.International journal of molecular sciences · 2025
    Review
  11. Review
  12. Survey of Dopamine Receptor D2 Antagonists as Retinal Antifibrotics.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2024
    Article
  13. Proliferative vitreoretinopathy: an update on the current and emerging treatment options.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2024
    Review
  14. Article
  15. Proliferative Vitreoretinopathy: A Reappraisal.Journal of clinical medicine · 2023
    Review
  16. Article
  17. Rhegmatogenous retinal detachment surgery: A review.Clinical & experimental ophthalmology · 2023
    Review
  18. Review
  19. Article
  20. Advances in Vitreoretinal Surgery.Journal of clinical medicine · 2022
    Review
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

9 authors at 3 institutions in 1 country.

Dhanesh AmarnaniSchepens Eye Research Institute of Massachusetts Eye and Ear, Boston, Massachusetts, United States.
Arturo Israel Machuca-ParraSchepens Eye Research Institute of Massachusetts Eye and Ear, Boston, Massachusetts, United States.
Lindsay L WongSchepens Eye Research Institute of Massachusetts Eye and Ear, Boston, Massachusetts, United States.
Christina K MarkoSchepens Eye Research Institute of Massachusetts Eye and Ear, Boston, Massachusetts, United States.
James A StefaterRetina Service, Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, United States.
Tomasz P StryjewskiRetina Service, Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, United States.
Dean EliottRetina Service, Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, United States.
Joseph F Arboleda-VelasquezSchepens Eye Research Institute of Massachusetts Eye and Ear, Boston, Massachusetts, United States.
Leo A KimSchepens Eye Research Institute of Massachusetts Eye and Ear, Boston, Massachusetts, United States.
Massachusetts Eye and Ear Infirmary · USSmith-Kettlewell Eye Research Institute · USHarvard University · US

Funding

VISION RESEARCHP30EY003790 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI Sunil K Chauhan · 1985 to 2026
$25.5M
Mass Eye and Ear-Vision Clinical Scientist Development ProgramK12EY016335 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Reza Dana · 2004 to 2026
$12.3M
Notch and TGF-beta in the Control of Retinal Vascular IntegrityR00EY021624 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI ARBOLEDA-VELASQUEZ, JOSEPH · 2014 to 2016
$736k
Vasculogenesis in Thyroid Eye DiseaseR21EY027061 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI KIM, LEO A · 2016 to 2017
$542k
NEI NIH HHS K12 EY016335NEI NIH HHS P30 EY003790NEI NIH HHS R00 EY021624NEI NIH HHS R21 EY027061
6 · The paper itself

Abstract

Purpose: The purpose of this study was to develop a method for isolating, culturing, and characterizing cells from patient-derived membranes in proliferative vitreoretinopathy (PVR) to be used for drug testing. Methods: PVR membranes were obtained from six patients with grade C PVR. Membrane fragments were analyzed by gross evaluation, fixed for immunohistologic studies to establish cell identity, or digested with collagenase II to obtain single cell suspensions for culture. PVR-derived primary cultures were used to examine the effects of methotrexate (MTX) on proliferation, migration, and cell death. Results: Gross analysis of PVR membranes showed presence of pigmented cells, indicative of retinal pigment epithelial cells. Immunohistochemistry identified cells expressing α-smooth muscle actin, glial fibrillary acidic protein, Bestrophin-1, and F4/80, suggesting the presence of multiple cell types in PVR. Robust PVR primary cultures (C-PVR) were successfully obtained from human membranes, and these cells retained the expression of cell identity markers in culture. C-PVR cultures formed membranes and band-like structures in culture reminiscent of the human condition. MTX significantly reduced the proliferation and band formation of C-PVR, whereas it had no significant effect on cell migration. MTX also induced regulated cell death within C-PVR as assessed by increased expression of caspase-3/7. Conclusions: PVR cells obtained from human membranes can be successfully isolated, cultured, and profiled in vitro. Using these primary cultures, we identified MTX as capable of significantly reducing growth and inducing cell death of PVR cells in vitro.

Indexed as

AdultAgedApoptosisBiomarkersCell Culture TechniquesCell MovementCell ProliferationCell SeparationEpiretinal MembraneExtracellular Matrix ProteinsFemaleFluorescent Antibody Technique, IndirectHumansImmunosuppressive AgentsMaleMethotrexateBiomarkersExtracellular Matrix ProteinsImmunosuppressive AgentsMethotrexateTumor Necrosis Factor-alpha

Identifiers

PMID28777835
PMCPMC5544356
OpenAlexW2737736503

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.