Evidence map›Paper›PMID 39120283›Full record

ArticleCells2024

miRNA-Driven Regulation of Endothelial-to-Mesenchymal Transition Differs among Thoracic Aortic Aneurysms.

Sonia Terriaca, Maria Giovanna Scioli, Fabio Bertoldo, Calogera Pisano, Paolo Nardi, Carmela Rita Balistreri, Daniele Magro, Beatrice Belmonte, Luca Savino, Amedeo Ferlosio and 1 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
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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

11 authors.

Sonia TerriacaAnatomic Pathology, Fondazione Policlinico Tor Vergata, 00133 Rome, Italy.
Maria Giovanna ScioliAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0002-8458-4108
Fabio BertoldoCardiac Surgery Unit, Department of Surgery, Tor Vergata University, 00133 Rome, Italy.
Calogera PisanoCardiac Surgery Unit, Department of Surgery, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0002-6488-1965
Paolo NardiCardiac Surgery Unit, Department of Surgery, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0002-4005-3110
Carmela Rita BalistreriCellular and Molecular Laboratory, Department of Biomedicine, Neuroscience and Advanced Diagnostics (Bi.N.D.), University of Palermo, 90134 Palermo, Italy.ORCID 0000-0002-5393-1007
Daniele MagroCellular and Molecular Laboratory, Department of Biomedicine, Neuroscience and Advanced Diagnostics (Bi.N.D.), University of Palermo, 90134 Palermo, Italy.
Beatrice BelmonteTumor Immunology Unit, Department of Health Sciences, University of Palermo, 90134 Palermo, Italy.ORCID 0000-0001-9668-0925
Luca SavinoAnatomic Pathology, Fondazione Policlinico Tor Vergata, 00133 Rome, Italy.ORCID 0000-0001-9068-2225
Amedeo FerlosioAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, 00133 Rome, Italy.
Augusto OrlandiAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0001-7202-5854

Funding

European Union PNRR-MR1-2022-12376699
6 · The paper itself

Abstract

Thoracic aortic aneurysms (TAAs) represent a serious health concern, as they are associated with early aortic dissection and rupture. TAA formation is triggered by genetic conditions, in particular Marfan syndrome (MFS) and bicuspid aortic valve (BAV). During the aneurysmatic process, aortic endothelial cells can undergo endothelial-to-mesenchymal transition (End-MT) with consequent phenotypic and functional alterations. We previously documented that MFS TAA is characterized by miR-632-driven End-MT exacerbation, whereas in BAV aortopathy, the occurrence of this process remains still controversial. We investigated the End-MT process and the underlined regulatory mechanisms in BAV, TAV and MFS TAA tissues. Gene expression and immunohistochemical analysis were performed in order to analyze some important miRNAs and genes characterizing End-MT. We documented that BAV endothelium maintains the expression of the endothelial homeostasis markers, such as

Indexed as

Aortic Aneurysm, ThoracicEpithelial-Mesenchymal TransitionMicroRNAsAdultAgedBicuspid Aortic Valve DiseaseEndothelial CellsFemaleGene Expression RegulationHumansMaleMarfan SyndromeMiddle AgedPlatelet Endothelial Cell Adhesion Molecule-1Transcriptional Regulator ERGERG protein, humanMicroRNAsMIRN126 microRNA, humanPlatelet Endothelial Cell Adhesion Molecule-1Transcriptional Regulator ERGbicuspid aortic valveendothelial cellsendothelial-to-mesenchymal transitionMarfan syndromemiR-126-5pmiR-632thoracic aortic aneurysmstissue and circulating miRNAs

Identifiers

PMID39120283
PMCPMC11312012

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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.