Evidence map›Paper›PMID 31426601›Full record

ReviewCells2019

The uPAR System as a Potential Therapeutic Target in the Diseased Eye.

Maurizio Cammalleri, Massimo Dal Monte, Vincenzo Pavone, Mario De Rosa, Dario Rusciano, Paola Bagnoli

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

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  7. Turn-Adopting Peptidomimetic as a Formyl Peptide Receptor-1 Antagonist.ACS pharmacology & translational science · 2024
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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 2 institutions in 1 country.

Maurizio CammalleriDipartimento di Biologia, Università di Pisa, 56127 Pisa, Italy.
Massimo Dal MonteDipartimento di Biologia, Università di Pisa, 56127 Pisa, Italy.ORCID 0000-0002-5181-4456
Vincenzo PavoneDipartimento di Scienze Chimiche, Università di Napoli Federico II, 80126 Napoli, Italy.
Mario De RosaDipartimento di Medicina Sperimentale, Università della Campania, 80138 Napoli, Italy.
Dario RuscianoSooft Italia SpA, Contrada Molino 17, 63833 Montegiorgio (FM), Italy.ORCID 0000-0002-9577-2585
Paola BagnoliDipartimento di Biologia, Università di Pisa, 56127 Pisa, Italy. paola.bagnoli@unipi.it.
University of Pisa · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of vascular networks is characteristic of eye diseases associated with retinal cell degeneration and visual loss. Visual impairment is also the consequence of photoreceptor degeneration in inherited eye diseases with a major inflammatory component, but without angiogenic profile. Among the pathways with high impact on vascular/degenerative diseases of the eye, a central role is played by a system formed by the ligand urokinase-type plasminogen activator (uPA) and its receptor uPAR. The uPAR system, although extensively investigated in tumors, still remains a key issue in vascular diseases of the eye and even less studied in inherited retinal pathologies such as retinitis pigmantosa (RP). Its spectrum of action has been extended far beyond a classical pro-angiogenic function and has emerged as a central actor in inflammation. Preclinical studies in more prevalent eye diseases characterized by neovascular formation, as in retinopathy of prematurity, wet macular degeneration and rubeosis iridis or vasopermeability excess as in diabetic retinopathy, suggest a critical role of increased uPAR signaling indicating the potentiality of its modulation to counteract neovessel formation and microvascular dysfunction. The additional observation that the uPAR system plays a major role in RP by limiting the inflammatory cascade triggered by rod degeneration rises further questions about its role in the diseased eye.

Indexed as

Receptors, Urokinase Plasminogen ActivatorRetinal DiseasesUrokinase-Type Plasminogen ActivatorAnimalsDisease Models, AnimalHumansInflammationMiceMice, Inbred BALB CNeovascularization, PathologicRatsRats, Sprague-DawleyReceptors, Urokinase Plasminogen ActivatorUrokinase-Type Plasminogen Activatorangiogenesisanimal modelsco-receptor signalinginflammationocular diseasesphotoreceptor degenerationretinal functionuPAR system blockadevascular leakage

Identifiers

PMID31426601
PMCPMC6721659
OpenAlexW2968170366

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.