Evidence map›Paper›PMID 40082360›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Isolation and Characterization of EVs Containing Mitochondria from OIS Cells.

Ines Martic, David Feldmann, Maria Cavinato

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Ines MarticInstitute for Biomedical Aging Research, University of Innsbruck, Innsbruck, Austria.
David FeldmannInstitute for Biomedical Aging Research, University of Innsbruck, Innsbruck, Austria.
Maria CavinatoInstitute for Biomedical Aging Research, University of Innsbruck, Innsbruck, Austria. Maria.Cavinato-Nascimento@uibk.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncogene activation triggers oncogene-induced senescence (OIS), a tumor-suppression mechanism characterized by mitochondrial dysfunction and the secretion of various factors collectively known as the senescence-associated secretory phenotype (SASP). Recent evidence highlights that extracellular vesicles (EVs), nanosized membrane-bound particles, are part of the SASP and act as a novel intercellular communication pathway. Additionally, EVs containing mitochondrial compartments are hypothesized to function as a mitochondrial quality control mechanism, eliminating damaged mitochondria in senescent cells. However, the exact role of mitochondria-enriched vesicles in OIS remains elucidated. The diversity of protocols for isolating and characterizing EVs complicates the unification of research findings. Here, we provide a concise overview of current protocols for investigating vesicles-containing mitochondria in oncogene-induced senescent cells including size exclusion chromatography, NTA analysis, flow cytometry, confocal microscopy, and Western blot.

Indexed as

Cellular SenescenceExtracellular VesiclesMitochondriaOncogenesBlotting, WesternChromatography, GelFlow CytometryHumansMicroscopy, ConfocalExtracellular vesiclesFlow cytometryMitochondriaNTASenescence

Identifiers

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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 OpenQuestion graph.