Evidence map›Paper›PMID 36428520›Full record

ArticleBiomedicines2022

Astrocytes-Derived Small Extracellular Vesicles Hinder Glioma Growth.

Carmela Serpe, Antonio Michelucci, Lucia Monaco, Arianna Rinaldi, Mariassunta De Luca, Pietro Familiari, Michela Relucenti, Erika Di Pietro, Maria Amalia Di Castro, Igea D'Agnano and 3 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Piezo1, the new actor in cell volume regulation.Pflugers Archiv : European journal of physiology · 2024
    Review
  9. 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

13 authors at 5 institutions in 1 country.

Carmela SerpeDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Antonio MichelucciDepartment of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
Lucia MonacoDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Arianna RinaldiDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Mariassunta De LucaDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Pietro FamiliariDivision of Neurosurgery, Department of Human Neurosciences, Policlinico Umberto I, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0003-0513-2312
Michela RelucentiDepartment of Anatomical, Histological, Forensic Medicine and Orthopedics Sciences, Sapienza University, 00185 Rome, Italy.ORCID 0000-0002-3805-9505
Erika Di PietroDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Maria Amalia Di CastroDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.ORCID 0000-0001-7480-1087
Igea D'AgnanoInstitute of Biomedical Technologies, CNR, 20054 Segrate, Italy.ORCID 0000-0002-2646-9224
Luigi CatacuzzenoDepartment of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
Cristina LimatolaDepartment of Physiology and Pharmacology, Laboratory Affiliated to Istituto Pasteur Italia Fondazione Cenci Bolognetti, Sapienza University, 00185 Rome, Italy.ORCID 0000-0001-7504-8197
Myriam CatalanoDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.ORCID 0000-0003-4638-9202
Sapienza University of Rome · ITUniversity of Perugia · ITInstitute of Biomedical Technologies · ITIstituto Pasteur · ITPoliclinico Umberto I · IT

Funding

Governo Italiano PRIN20178L7WRSGoverno Italiano PRIN2020Z73J5AItalian Association for Cancer Research IG-23010Sapienza University of Rome RM12117A80E90BF3
6 · The paper itself

Abstract

All cells are capable of secreting extracellular vesicles (EVs), which are not a means to eliminate unneeded cellular compounds but represent a process to exchange material (nucleic acids, lipids and proteins) between different cells. This also happens in the brain, where EVs permit the crosstalk between neuronal and non-neuronal cells, functional to homeostatic processes or cellular responses to pathological stimuli. In brain tumors, EVs are responsible for the bidirectional crosstalk between glioblastoma cells and healthy cells, and among them, astrocytes, that assume a pro-tumoral or antitumoral role depending on the stage of the tumor progression. In this work, we show that astrocyte-derived small EVs (sEVs) exert a defensive mechanism against tumor cell growth and invasion. The effect is mediated by astrocyte-derived EVs (ADEVs) through the transfer to tumor cells of factors that hinder glioma growth. We identified one of these factors, enriched in ADEVs, that is miR124. It reduced both the expression and function of the volume-regulated anion channel (VRAC), that, in turn, decreased the cell migration and invasion of murine glioma GL261 cells.

Indexed as

astrocytesgliomamiR124small extracellular vesiclesvolume-regulated anion channels

Identifiers

PMID36428520
PMCPMC9688032
OpenAlexW4309174528

What OpenQuestion holds

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Registered trials

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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.