Evidence map›Paper›PMID 36769281›Full record

ArticleInternational journal of molecular sciences2023

Role of Uric Acid in Vascular Remodeling: Cytoskeleton Changes and Migration in VSMCs.

Elisa Russo, Maria Bertolotto, Valentina Zanetti, Daniela Picciotto, Pasquale Esposito, Federico Carbone, Fabrizio Montecucco, Roberto Pontremoli, Giacomo Garibotto, Francesca Viazzi and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Serum Uric Acid/Serum Creatinine Ratio and Chronic Vascular Lesions on Renal Biopsy: A Retrospective Observational Study.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2025
    Observational
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

11 authors.

Elisa RussoNephrology and Dialysis Unit, San Luca Hospital, 55100 Lucca, Italy.ORCID 0000-0003-1279-3178
Maria BertolottoDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.
Valentina ZanettiIRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Daniela PicciottoIRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Pasquale EspositoDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.ORCID 0000-0002-0834-5586
Federico CarboneDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.ORCID 0000-0003-2957-4078
Fabrizio MontecuccoDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.ORCID 0000-0003-0823-8729
Roberto PontremoliDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.ORCID 0000-0003-1238-872X
Giacomo GaribottoDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.ORCID 0000-0001-6432-2429
Francesca ViazziDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.ORCID 0000-0003-4219-7043
Daniela VerzolaDepartment of Internal Medicine, University of Genoa, 16132 Genoa, Italy.

Funding

Fondazione Cassa di Risparmio di Genova e Imperia D.R. 3707
6 · The paper itself

Abstract

The mechanisms by which hyperuricemia induces vascular dysfunction and contributes to cardiovascular disease are still debated. Phenotypic transition is a property of vascular smooth muscle cells (VSMCs) involved in organ damage. The aim of this study was to investigate the effects of uric acid (UA) on changes in the VSMC cytoskeleton, cell migration and the signals involved in these processes. MOVAS, a mouse VSMC line, was incubated with 6, 9 and 12 mg/dL of UA, angiotensin receptor blockers (ARBs), proteasome and MEK-inhibitors. Migration property was assessed in a micro-chemotaxis chamber and by phalloidin staining. Changes in cytoskeleton proteins (Smoothelin B (SMTB), alpha-Smooth Muscle Actin (αSMA), Smooth Muscle 22 Alpha (SM22α)), Atrogin-1 and MAPK activation were determined by Western blot, immunostaining and quantitative reverse transcription PCR. UA exposition modified SMT, αSMA and SM22α levels (

Indexed as

Muscle, Smooth, VascularUric AcidAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAnimalsCell MovementCell ProliferationCells, CulturedCytoskeletonMiceMyocytes, Smooth MuscleProteasome Endopeptidase ComplexVascular RemodelingAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsProteasome Endopeptidase ComplexUric Acidmigrationphenotypic transitionuric acidvascular remodelingvascular smooth muscle cell

Identifiers

PMID36769281
PMCPMC9917405

What OpenQuestion holds

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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.