Evidence map›Paper›PMID 36231082›Full record

ArticleCells2022

Platelet-Derived Extracellular Vesicles Stimulate Migration through Partial Remodelling of the Ca

Mauro Vismara, Sharon Negri, Francesca Scolari, Valentina Brunetti, Silvia Maria Grazia Trivigno, Pawan Faris, Luca Galgano, Teresa Soda, Roberto Berra-Romani, Ilaria Canobbio and 3 more

Abstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Therapeutic Potential of Extracellular Vesicles in Oral Inflammation.International journal of molecular sciences · 2025
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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.

Mauro VismaraLaboratory of Biochemistry, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Sharon NegriLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Francesca ScolariInstitute of Molecular Genetics, Italian National Research Council (CNR), 27100 Pavia, Italy.ORCID 0000-0003-3085-9038
Valentina BrunettiLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Silvia Maria Grazia TrivignoLaboratory of Biochemistry, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Pawan FarisLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.ORCID 0000-0001-6867-0359
Luca GalganoLaboratory of Biochemistry, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Teresa SodaDepartment of Health Sciences, University of Magna Graecia, 88100 Catanzaro, Italy.
Roberto Berra-RomaniDepartment of Biomedicine, School of Medicine, Benemérita Universidad Autónoma de Puebla, Puebla 74325, Mexico.ORCID 0000-0003-4884-0925
Ilaria CanobbioLaboratory of Biochemistry, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.ORCID 0000-0002-9643-3403
Mauro TortiLaboratory of Biochemistry, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Gianni Francesco GuidettiLaboratory of Biochemistry, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.ORCID 0000-0003-4800-4564
Francesco MocciaLaboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.ORCID 0000-0003-0010-0098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlatelets can support cancer progression via the release of microparticles and microvesicles that enhance the migratory behaviour of recipient cancer cells. We recently showed that platelet-derived extracellular vesicles (PEVs) stimulate migration and invasiveness in highly metastatic MDA-MB-231 cells by stimulating the phosphorylation of p38 MAPK and the myosin light chain 2 (MLC2). Herein, we assessed whether the pro-migratory effect of PEVs involves the remodelling of the Ca

methodsPEVs were isolated from human blood platelets, and Fura-2/AM Ca

resultsPretreating MDA-MB-231 cells with PEVs for 24 h caused an increase in Ca

conclusionsPEVs stimulate migration in the highly metastatic MDA-MB-231 breast cancer cell line by inducing a partial remodelling of the Ca

Indexed as

Breast NeoplasmsExtracellular VesiclesBlood PlateletsCalciumCell Line, TumorFemaleFura-2Humansp38 Mitogen-Activated Protein KinasesCalciumFura-2p38 Mitogen-Activated Protein Kinasesbreast cancerCa2+ signallingextracellular vesiclesInsP3 receptorsmigrationmyosin light chain 2p38 mitogen-activated protein kinaseplateletsSERCA2B

Identifiers

PMID36231082
PMCPMC9564117

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.