Evidence map›Paper›PMID 27994032›Full record

ArticleNucleic acids research2017

Rapid decay of engulfed extracellular miRNA by XRN1 exonuclease promotes transient epithelial-mesenchymal transition.

Joséphine Zangari, Marius Ilie, Florian Rouaud, Laurie Signetti, Mickaël Ohanna, Robin Didier, Barnabé Roméo, Dana Goldoni, Nicolas Nottet, Cathy Staedel and 5 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Joséphine ZangariUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Marius IlieUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Florian RouaudUniversité Côte d'Azur, INSERM, C3M, 06200 Nice, France.
Laurie SignettiUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Mickaël OhannaUniversité Côte d'Azur, INSERM, C3M, 06200 Nice, France.
Robin DidierUniversité Côte d'Azur, INSERM, C3M, 06200 Nice, France.
Barnabé RoméoUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Dana GoldoniUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Nicolas NottetUniversité Côte d'Azur, CNRS, INSERM, IPMC, FHU-OncoAge, 06560 Valbonne, France.
Cathy StaedelUniversité de Bordeaux, INSERM, ARNA, 33076 Bordeaux, France.
Jocelyn GalAntoine Lacassagne Cancer Center, Epidemiology and Biostatistics Unit, 06189 Nice, France.
Bernard MariUniversité Côte d'Azur, CNRS, INSERM, IPMC, FHU-OncoAge, 06560 Valbonne, France.
Baharia MograbiUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Paul HofmanUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Patrick BrestUniversité Côte d'Azur, CNRS, INSERM, IRCAN, FHU-OncoAge, 06107 Nice France.
Centre National de la Recherche Scientifique · FRInserm · FRCentre Antoine Lacassagne · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) have been shown to play an important role in intercellular communication as carriers of DNA, RNA and proteins. While the intercellular transfer of miRNA through EVs has been extensively studied, the stability of extracellular miRNA (ex-miRNA) once engulfed by a recipient cell remains to be determined. Here, we identify the ex-miRNA-directed phenotype to be transient due to the rapid decay of ex-miRNA. We demonstrate that the ex-miR-223-3p transferred from polymorphonuclear leukocytes to cancer cells were functional, as demonstrated by the decreased expression of its target FOXO1 and the occurrence of epithelial-mesenchymal transition reprogramming. We showed that the engulfed ex-miRNA, unlike endogenous miRNA, was unstable, enabling dynamic regulation and a return to a non-invasive phenotype within 8 h. This transient phenotype could be modulated by targeting XRN1/PACMAN exonuclease. Indeed, its silencing was associated with slower decay of ex-miR-223-3p and subsequently prolonged the invasive properties. In conclusion, we showed that the 'steady step' level of engulfed miRNA and its subsequent activity was dependent on the presence of a donor cell in the surroundings to constantly fuel the recipient cell with ex-miRNAs and of XRN1 exonuclease, which is involved in the decay of these imported miRNA.

Indexed as

RNA StabilityCell Line, TumorEpithelial-Mesenchymal TransitionExoribonucleasesExosomesHumansMicroRNAsMicrotubule-Associated ProteinsNeoplasm InvasivenessNeoplasmsNeutrophilsExoribonucleasesMicroRNAsMicrotubule-Associated ProteinsMIR223, humanXRN1 protein, human

Identifiers

PMID27994032
PMCPMC5397191
OpenAlexW2563481002

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.