Evidence map›Paper›PMID 38138924›Full record

ArticleJournal of personalized medicine2023

Transcriptomic Analysis of Tight Junction Proteins Demonstrates the Aberrant Expression and Function of Zona Occludens 2 (ZO-2) Protein in Stanford Type A Aortic Dissection.

Dimitrios E Magouliotis, Arian Arjomandi Rad, Antonios Kourliouros, Alessandro Viviano, Marinos Koulouroudias, Mohammad Yousuf Salmasi, Alexandros Briasoulis, Filippos Triposkiadis, John Skoularigis, Thanos Athanasiou

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

10 authors at 7 institutions in 3 countries.

Dimitrios E MagouliotisUnit of Quality Improvement, Department of Cardiothoracic Surgery, University of Thessaly, 41110 Biopolis, Greece.ORCID 0000-0001-5417-6392
Arian Arjomandi RadDepartment of Surgery and Cancer, Imperial College London, St Mary's Hospital, London W2 1NY, UK.ORCID 0000-0002-4931-4049
Antonios KourliourosDepartment of Cardiothoracic Surgery, Oxford University Hospitals, Oxford OX3 9DU, UK.
Alessandro VivianoDepartment of Cardiac Surgery, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London W2 1NY, UK.
Marinos KoulouroudiasDepartment of Cardiac Surgery, Nottingham University Hospitals NHS Trust, Nottingham NG5 1PB, UK.ORCID 0000-0003-0592-0319
Mohammad Yousuf SalmasiDepartment of Surgery and Cancer, Imperial College London, St Mary's Hospital, London W2 1NY, UK.
Alexandros BriasoulisDepartment of Therapeutics, Faculty of Medicine, National and Kapodistrian University of Athens, 10679 Athens, Greece.ORCID 0000-0002-5740-9670
Filippos TriposkiadisSchool of Medicine, European University Cyprus, Nicosia 2404, Cyprus.ORCID 0000-0001-6433-4016
John SkoularigisDepartment of Cardiology, University of Thessaly, Biopolis, 41110 Larissa, Greece.ORCID 0000-0001-7159-2478
Thanos AthanasiouDepartment of Surgery and Cancer, Imperial College London, St Mary's Hospital, London W2 1NY, UK.
St Mary's Hospital · GBUniversity of Thessaly · GREuropean University Cyprus · CYImperial College Healthcare NHS Trust · GBNational and Kapodistrian University of Athens · GRNottingham University Hospitals NHS Trust · GBOxford University Hospitals NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThoracic aortic aneurysm dissection (TAAD) represents a cardiac surgery emergency characterized by the disrupted integrity of the aortic wall and is associated with poor prognosis. In this context, the identification of biomarkers implicated in the pathobiology of TAAD is crucial. Our aim in the present original in silico study is to assess the differential gene expression profile of the tight junction proteins (TJPs) in patients with TAAD and to propose novel biomarkers for the diagnosis and prognosis of this disease.

methodsWe implemented bioinformatics methodology in order to construct the gene network of the TJPs family, identify the differentially expressed genes (DEGs) in pathologic aortic tissue excised from patients with TAAD as compared to healthy aortic tissue, and assess the related biological functions and the associated miRNA families.

resultsData regarding the transcriptomic profile of selected genes were retrieved and incorporated from three microarray datasets, including 23 TAAD and 20 healthy control samples. A total of 32 TJPs were assessed. The zona occludens 2 (ZO-2) protein encoded by the gene TJP2 was significantly under-expressed in patients with TAAD compared to the control group (

conclusionsThese outcomes demonstrated the important role of ZO-2 in the pathobiology of TAAD.

Indexed as

biomarkermiRNAthoracic aortic dissectionTJP2ZO-2zona occludens 2

Identifiers

PMID38138924
PMCPMC10744791
OpenAlexW4389565342

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.