Evidence map›Paper›PMID 29109268›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Syntenin mediates SRC function in exosomal cell-to-cell communication.

Naga Sailaja Imjeti, Kerstin Menck, Antonio Luis Egea-Jimenez, Celine Lecointre, Frederique Lembo, Habib Bouguenina, Ali Badache, Rania Ghossoub, Guido David, Serge Roche and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

90 citing papers in PubMed, 150 citations in OpenAlex.

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30 more citing papers are in PubMed but not listed here.

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

11 authors at 1 institution in 2 countries.

Naga Sailaja ImjetiDepartment of Human Genetics, K. U. Leuven, B-3000 Leuven, Belgium.
Kerstin MenckCentre de Recherche en Cancérologie de Marseille (CRCM), Aix-Marseille Université, Marseille F-13284, France.ORCID 0000-0002-8188-0163
Antonio Luis Egea-JimenezDepartment of Human Genetics, K. U. Leuven, B-3000 Leuven, Belgium.
Celine LecointreCNRS Université Montpellier, Centre de Recherche en Biologie Cellulaire de Montpellier, 34000 Montpellier, France.
Frederique LemboCentre de Recherche en Cancérologie de Marseille (CRCM), Aix-Marseille Université, Marseille F-13284, France.
Habib BougueninaCentre de Recherche en Cancérologie de Marseille (CRCM), Aix-Marseille Université, Marseille F-13284, France.
Ali BadacheCentre de Recherche en Cancérologie de Marseille (CRCM), Aix-Marseille Université, Marseille F-13284, France.ORCID 0000-0001-7710-2505
Rania GhossoubCentre de Recherche en Cancérologie de Marseille (CRCM), Aix-Marseille Université, Marseille F-13284, France.
Guido DavidDepartment of Human Genetics, K. U. Leuven, B-3000 Leuven, Belgium.
Serge RocheCNRS Université Montpellier, Centre de Recherche en Biologie Cellulaire de Montpellier, 34000 Montpellier, France.
Pascale ZimmermannDepartment of Human Genetics, K. U. Leuven, B-3000 Leuven, Belgium; pascale.zimmermann@kuleuven.be.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cytoplasmic tyrosine kinase SRC controls cell growth, proliferation, adhesion, and motility. The current view is that SRC acts primarily downstream of cell-surface receptors to control intracellular signaling cascades. Here we reveal that SRC functions in cell-to-cell communication by controlling the biogenesis and the activity of exosomes. Exosomes are viral-like particles from endosomal origin that can reprogram recipient cells. By gain- and loss-of-function studies, we establish that SRC stimulates the secretion of exosomes having promigratory activity on endothelial cells and that syntenin is mandatory for SRC exosomal function. Mechanistically, SRC impacts on syndecan endocytosis and on syntenin-syndecan endosomal budding, upstream of ARF6 small GTPase and its effector phospholipase D2, directly phosphorylating the conserved juxtamembrane DEGSY motif of the syndecan cytosolic domain and syntenin tyrosine 46. Our study uncovers a function of SRC in cell-cell communication, supported by syntenin exosomes, which is likely to contribute to tumor-host interactions.

Indexed as

ADP-Ribosylation Factor 6ADP-Ribosylation FactorsAmino Acid MotifsCell CommunicationCell MovementCell ProliferationCulture Media, ConditionedEndocytosisEndosomesExosomesGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsMCF-7 CellsOncogene Protein pp60(v-src)Phospholipase DADP-Ribosylation Factor 6ADP-Ribosylation FactorsARF6 protein, humanCulture Media, ConditionedOncogene Protein pp60(v-src)Phospholipase Dphospholipase D2SyndecansSynteninsARF6exosomeSRCsyndecansyntenin

Identifiers

PMID29109268
PMCPMC5703317
OpenAlexW2767903251

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.