Evidence map›Paper›PMID 33692478›Full record

ArticleScientific reports2021

Protein network analyses of pulmonary endothelial cells in chronic thromboembolic pulmonary hypertension.

Sarath Babu Nukala, Olga Tura-Ceide, Giancarlo Aldini, Valérie F E D Smolders, Isabel Blanco, Victor I Peinado, Manuel Castellà, Joan Albert Barberà, Alessandra Altomare, Giovanna Baron and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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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

13 authors at 5 institutions in 2 countries.

Sarath Babu Nukala *Department of Pharmaceutical Sciences, Università Degli Studi Di Milano, 20133, Milan, Italy. sarath.nukala@unimi.it.
Olga Tura-Ceide *Department of Pulmonary Medicine, Hospital Clínic-Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Giancarlo AldiniDepartment of Pharmaceutical Sciences, Università Degli Studi Di Milano, 20133, Milan, Italy.
Valérie F E D SmoldersDepartment of Biochemistry and Molecular Biomedicine and Institute of Biomedicine (IBUB), Faculty of Biology, University of Barcelona, Barcelona, Spain.
Isabel BlancoDepartment of Pulmonary Medicine, Hospital Clínic-Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Victor I PeinadoDepartment of Pulmonary Medicine, Hospital Clínic-Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Manuel CastellàDepartment of Cardiovascular Surgery, Institut Clínic del Tòrax, Hospital Clínic, University of Barcelona, Barcelona, Spain.
Joan Albert BarberàDepartment of Pulmonary Medicine, Hospital Clínic-Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Alessandra AltomareDepartment of Pharmaceutical Sciences, Università Degli Studi Di Milano, 20133, Milan, Italy.
Giovanna BaronDepartment of Pharmaceutical Sciences, Università Degli Studi Di Milano, 20133, Milan, Italy.
Marina CariniDepartment of Pharmaceutical Sciences, Università Degli Studi Di Milano, 20133, Milan, Italy.
Marta Cascante *Department of Biochemistry and Molecular Biomedicine and Institute of Biomedicine (IBUB), Faculty of Biology, University of Barcelona, Barcelona, Spain.
Alfonsina D'Amato *Department of Pharmaceutical Sciences, Università Degli Studi Di Milano, 20133, Milan, Italy. alfonsina.damato@unimi.it.
University of Milan · ITUniversitat de Barcelona · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic thromboembolic pulmonary hypertension (CTEPH) is a vascular disease characterized by the presence of organized thromboembolic material in pulmonary arteries leading to increased vascular resistance, heart failure and death. Dysfunction of endothelial cells is involved in CTEPH. The present study describes for the first time the molecular processes underlying endothelial dysfunction in the development of the CTEPH. The advanced analytical approach and the protein network analyses of patient derived CTEPH endothelial cells allowed the quantitation of 3258 proteins. The 673 differentially regulated proteins were associated with functional and disease protein network modules. The protein network analyses resulted in the characterization of dysregulated pathways associated with endothelial dysfunction, such as mitochondrial dysfunction, oxidative phosphorylation, sirtuin signaling, inflammatory response, oxidative stress and fatty acid metabolism related pathways. In addition, the quantification of advanced oxidation protein products, total protein carbonyl content, and intracellular reactive oxygen species resulted increased attesting the dysregulation of oxidative stress response. In conclusion this is the first quantitative study to highlight the involvement of endothelial dysfunction in CTEPH using patient samples and by network medicine approach.

Indexed as

Protein CarbonylationProtein Interaction MapsEndothelial CellsHumansHypertension, PulmonaryPulmonary ArteryPulmonary EmbolismThromboembolism

Identifiers

PMID33692478
PMCPMC7946953
OpenAlexW3135478617

What Socratic 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 Socratic graph.