Evidence map›Paper›PMID 31069271›Full record

ArticleCommunications biology2019

P38 inhibition reverses TGFβ1 and TNFα-induced contraction in a model of proliferative vitreoretinopathy.

Lauren Schiff, Nathan C Boles, Marie Fernandes, Bar Nachmani, Ronald Gentile, Timothy A Blenkinsop

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. The critical role of LRG1 in pathological fibrosis.Journal of molecular medicine (Berlin, Germany) · 2025
    Review
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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 3 institutions in 1 country.

Lauren Schiff1Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.
Nathan C Boles3Neural Stem Cell Institute, Rensselaer, NY 12144 USA.
Marie Fernandes1Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.
Bar Nachmani1Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.
Ronald Gentile1Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.
Timothy A Blenkinsop1Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.ORCID 0000-0002-8095-9937
New York Stem Cell Foundation · USIcahn School of Medicine at Mount Sinai · USNeural Stem Cell Institute · US

Funding

Reversing Contractility in Epiretinal MembranesR01EY029736 · NEI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BLENKINSOP, TIMOTHY A. · 2020 to 2024
$2.0M
NEI NIH HHS R01 EY029736
6 · The paper itself

Abstract

Proliferative vitreoretinopathy (PVR) is a metaplasia in the vitreous of the eye manifested by the transformation of retinal pigment epithelial (RPE) cells and the development of contracting epiretinal membranes (ERM), which lead to retinal detachment and vision loss. While TGFβ1 and TNFα have been associated with PVR, here we show that these cytokines act synergistically to induce an aggressive contraction phenotype on adult human (ah)RPE. Connected RPE detach upon contraction and form motile membranes that recruit more cells. TGFβ1 and TNFα (TNT)-induced contracting membranes uniquely express muscle and extracellular rearrangement genes. Whole transcriptome RNA sequencing of patient-dissected PVR membranes showed activation of the p38-MAPK signaling pathway. Inhibition of p38 during TNT treatment blocks ahRPE transformation and membrane contraction. Furthermore, TNT-induced membrane contractility can be reversed by p38 inhibition after induction. Therefore, targeting the p38-MAPK pathway may have therapeutic benefits for patients with PVR even after the onset of contracting ERMs.

Indexed as

AdultAgedAged, 80 and overCell MovementEpiretinal MembraneEpithelial CellsFemaleGene Expression RegulationHumansMaleMiddle AgedModels, Biologicalp38 Mitogen-Activated Protein KinasesPrimary Cell CultureRetinal DetachmentRetinal Pigment Epitheliump38 Mitogen-Activated Protein KinasesRNA, Small InterferingTGFB1 protein, humanTransforming Growth Factor beta1Tumor Necrosis Factor-alphaCollective cell migrationMechanisms of disease

Identifiers

PMID31069271
PMCPMC6499805
OpenAlexW2943255343

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.