Evidence map›Paper›PMID 34827604›Full record

ArticleBiomolecules2021

Diagnostic and Prognostic Utility of the Extracellular Vesicles Subpopulations Present in Pleural Effusion.

Joman Javadi, André Görgens, Hanna Vanky, Dhanu Gupta, Anders Hjerpe, Samir El-Andaloussi, Daniel Hagey, Katalin Dobra

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  6. Epigenetic regulation of pulmonary inflammation.Seminars in cell & developmental biology · 2024
    Review
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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

8 authors at 1 institution in 1 country.

Joman JavadiDivision of Pathology, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.ORCID 0000-0002-7876-0945
André GörgensDivision of BCM, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.ORCID 0000-0001-9198-0857
Hanna VankyDivision of Pathology, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.
Dhanu GuptaDivision of BCM, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.
Anders HjerpeDivision of Pathology, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.
Samir El-AndaloussiDivision of BCM, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.
Daniel HageyDivision of BCM, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.ORCID 0000-0001-9246-6235
Katalin DobraDivision of Pathology, Department of Laboratory Medicine, Karolinska Institutet, 141 52 Stockholm, Sweden.
Karolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs), comprising exosomes, microvesicles, and apoptotic bodies, are released by all cells into the extracellular matrix and body fluids, where they play important roles in intercellular communication and matrix remodeling in various pathological conditions. Malignant pleural mesothelioma (MPM) is a primary tumor of mesothelial origin, predominantly related to asbestos exposure. The detection of MPM at an early stage and distinguishing it from benign conditions and metastatic adenocarcinomas (AD) is sometimes challenging. Pleural effusion is often the first available biological material and an ideal source for characterizing diagnostic and prognostic factors. Specific proteins have previously been identified as diagnostic markers in effusion, but it is not currently known whether these are associated with vesicles or released in soluble form. Here, we study and characterize tumor heterogeneity and extracellular vesicle diversity in pleural effusion as diagnostic or prognostic markers for MPM. We analyzed extracellular vesicles and soluble proteins from 27 pleural effusions, which were collected and processed at the department of pathology and cytology at Karolinska University Hospital, representing three different patient groups, MPM (

Indexed as

Biomarkers, TumorExtracellular VesiclesPleural EffusionAgedAged, 80 and overExosomesFemaleHumansLung NeoplasmsMaleMesotheliomaMesothelioma, MalignantMiddle AgedPleural Effusion, MalignantPrognosisBiomarkers, Tumorbiomarkersextracellular vesiclesmalignant pleural mesotheliomapleural effusion

Identifiers

PMID34827604
PMCPMC8615485
OpenAlexW3209981445

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.