Evidence map›Paper›PMID 28811546›Full record

ArticleScientific reports2017

Serum-derived extracellular vesicles (EVs) impact on vascular remodeling and prevent muscle damage in acute hind limb ischemia.

Claudia Cavallari, Andrea Ranghino, Marta Tapparo, Massimo Cedrino, Federico Figliolini, Cristina Grange, Valentina Giannachi, Paolo Garneri, Maria Chiara Deregibus, Federica Collino and 3 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04652531 (Autologous Serum-derived Extracellular Vesicles to Treat Venous Trophic Lesions Not Responsive to Conventional Treatments), which is not on this map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.2field-weighted citation impact, top 11% 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.

NCT04652531 naunknown statusnot on this mapstarted 2020, after this paper: background citation

Autologous Serum-derived Extracellular Vesicles to Treat Venous Trophic Lesions Not Responsive to Conventional Treatments

TypeinterventionalSponsorUniversity of Turin, ItalyRan2020 to 2024Enrolled10ConditionsUlcer VenousArmsAutologous extracellular vesicles from serum
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 70 citations in OpenAlex.

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  18. Extracellular vesicles in vascular remodeling.Acta pharmacologica Sinica · 2022
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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 2 institutions in 2 countries.

Claudia CavallariDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Andrea RanghinoDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Marta TapparoDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Massimo CedrinoDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Federico FiglioliniDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Cristina GrangeDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Valentina GiannachiDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Paolo GarneriDepartment of Surgical Sciences, University of Turin, Turin, Italy.
Maria Chiara DeregibusDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Federica CollinoDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy.
Pietro RispoliDepartment of Surgical Sciences, University of Turin, Turin, Italy.
Giovanni CamussiDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy. giovanni.camussi@unito.it.
Maria Felice BrizziDepartment of Medical Sciences, 2i3T Scarl, University of Turin, Turin, Italy. mariafelice.brizzi@unito.it.ORCID 0000-0003-0944-6992
University of Turin · ITDepartment of Medical Sciences · BY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serum is an abundant and accessible source of circulating extracellular vesicles (EVs). Serum-EV (sEV) pro-angiogenic capability and mechanisms are herein analyzed using an in vitro assay which predicts sEV angiogenic potential in vivo. Effective sEVs (e-sEVs) also improved vascular remodeling and prevented muscle damage in a mouse model of acute hind limb ischemia. e-sEV angiogenic proteomic and transcriptomic analyses show a positive correlation with matrix-metalloproteinase activation and extracellular matrix organization, cytokine and chemokine signaling pathways, Insulin-like Growth Factor and platelet pathways, and Vascular Endothelial Growth Factor signaling. A discrete gene signature, which highlights differences in e-sEV and ineffective-EV biological activity, was identified using gene ontology (GO) functional analysis. An enrichment of genes associated with the Transforming Growth Factor beta 1 (TGFβ1) signaling cascade is associated with e-sEV administration but not with ineffective-EVs. Chromatin immunoprecipitation analysis on the inhibitor of DNA binding I (ID1) promoter region, and the knock-down of small mother against decapentaplegic (SMAD)1-5 proteins confirmed GO functional analyses. This study demonstrates sEV pro-angiogenic activity, validates a simple, sEV pro-angiogenic assay which predicts their biological activity in vivo, and identifies the TGFβ1 cascade as a relevant mediator. We propose serum as a readily available source of EVs for therapeutic purposes.

Indexed as

Vascular RemodelingAnimalsBiomarkersCell ProliferationDisease Models, AnimalEndothelial CellsExtracellular VesiclesGene Expression ProfilingGene Expression RegulationHindlimbImmunohistochemistryIschemiaMiceMuscle, SkeletalNeovascularization, PhysiologicPromoter Regions, GeneticBiomarkers

Identifiers

PMID28811546
PMCPMC5557987
OpenAlexW2745014290

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.