Evidence map›Paper›PMID 34440835›Full record

ArticleCells2021

Microglia-Derived Small Extracellular Vesicles Reduce Glioma Growth by Modifying Tumor Cell Metabolism and Enhancing Glutamate Clearance through miR-124.

Carmela Serpe, Lucia Monaco, Michela Relucenti, Ludovica Iovino, Pietro Familiari, Ferdinando Scavizzi, Marcello Raspa, Giuseppe Familiari, Laura Civiero, Igea D'Agnano and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  20. Microglia in Glioma.Advances in neurobiology · 2024
    Review
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

12 authors at 5 institutions in 1 country.

Carmela SerpeDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Lucia MonacoDepartment of Physiology and Pharmacology, Sapienza University, 00185 Rome, Italy.
Michela RelucentiDepartment of Anatomical, Histological, Forensic Medicine and Orthopedics Sciences, Sapienza University, 00185 Rome, Italy.ORCID 0000-0002-3805-9505
Ludovica IovinoDepartment of Biology, University of Padova, 35131 Padova, Italy.
Pietro FamiliariDepartment of Human Neurosciences, Division of Neurosurgery, Sapienza University, 00185 Rome, Italy.ORCID 0000-0003-0513-2312
Ferdinando ScavizziInstitute of Biochemistry and Cell Biology (IBBC), CNR, 00015 Monterotond, Italy.
Marcello RaspaInstitute of Biochemistry and Cell Biology (IBBC), CNR, 00015 Monterotond, Italy.ORCID 0000-0002-3437-2430
Giuseppe FamiliariDepartment of Anatomical, Histological, Forensic Medicine and Orthopedics Sciences, Sapienza University, 00185 Rome, Italy.
Laura CivieroDepartment of Biology, University of Padova, 35131 Padova, Italy.
Igea D'AgnanoInstitute of Biomedical Technologies, CNR, 20054 Segrate, Italy.ORCID 0000-0002-2646-9224
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.
Sapienza University of Rome · ITInstitute of Cell Biology and Neurobiology · ITUniversity of Padua · ITInstitute of Biomedical Technologies · ITIstituto Neurologico Mediterraneo · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG-23010
6 · The paper itself

Abstract

Brain homeostasis needs continuous exchange of intercellular information among neurons, glial cells, and immune cells, namely microglial cells. Extracellular vesicles (EVs) are active players of this process. All the cells of the body, including the brain, release at least two subtypes of EVs, the medium/large EVs (m/lEVs) and small EVs (sEVs). sEVs released by microglia play an important role in brain patrolling in physio-pathological processes. One of the most common and malignant forms of brain cancer is glioblastoma. Altered intercellular communications constitute a base for the onset and the development of the disease. In this work, we used microglia-derived sEVs to assay their effects in vitro on murine glioma cells and in vivo in a glioma model on C57BL6/N mice. Our findings indicated that sEVs carry messages to cancer cells that modify glioma cell metabolism, reducing lactate, nitric oxide (NO), and glutamate (Glu) release. sEVs affect Glu homeostasis, increasing the expression of Glu transporter Glt-1 on astrocytes. We demonstrated that these effects are mediated by miR-124 contained in microglia-released sEVs. The in vivo benefit of microglia-derived sEVs results in a significantly reduced tumor mass and an increased survival of glioma-bearing mice, depending on miR-124.

Indexed as

AnimalsAntagomirsBrain NeoplasmsCell ProliferationCells, CulturedExcitatory Amino Acid Transporter 2Extracellular VesiclesGliomaGlutamic AcidInterferon-gammaKaplan-Meier EstimateLipopolysaccharidesMaleMiceMice, Inbred C57BLMicrogliaAntagomirsExcitatory Amino Acid Transporter 2Glutamic AcidInterferon-gammaLipopolysaccharidesMicroRNAsMirn124 microRNA, mouseNitric OxideSlc1a2 protein, mousebrain tumorsextracellular vesiclesgliomaGlt-1glutamatemicrogliamiR-124neurotoxicity

Identifiers

PMID34440835
PMCPMC8393731
OpenAlexW3190282823

What OpenQuestion 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 OpenQuestion graph.