Evidence map›Paper›PMID 32152404›Full record

ArticleOncogene2020

Vimentin prevents a miR-dependent negative regulation of tissue factor mRNA during epithelial-mesenchymal transitions and facilitates early metastasis.

Marie-Emilie Francart, Aline M Vanwynsberghe, Justine Lambert, Morgane Bourcy, Anthony Genna, Julien Ancel, Jennifer Perez-Boza, Agnès Noël, Philippe Birembaut, Ingrid Struman and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  5. Review
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  11. Tissue factor: a neglected role in cancer biology.Journal of thrombosis and thrombolysis · 2022
    Review
  12. Article
  13. Impact of Vimentin on Regulation of Cell Signaling and Matrix Remodeling.Frontiers in cell and developmental biology · 2022
    Review
  14. Review
  15. Article
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  17. Article
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 2 institutions in 2 countries.

Marie-Emilie Francart *GIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium.
Aline M Vanwynsberghe *GIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium.
Justine LambertGIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium.
Morgane BourcyGIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium.
Anthony GennaGIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium.
Julien AncelHôpital Maison Blanche, Service de pneumologie, CHU de Reims, 51092, Reims, France.
Jennifer Perez-BozaGIGA-Cancer, Molecular Angiogenesis Laboratory, University of Liège, Liège, Belgium.
Agnès NoëlGIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium.
Philippe BirembautINSERM, P3Cell UMR-S1250, SFR CAP-SANTE, Université de Reims Champagne-Ardenne, 51097, Reims, France.
Ingrid StrumanGIGA-Cancer, Molecular Angiogenesis Laboratory, University of Liège, Liège, Belgium.
Myriam PoletteINSERM, P3Cell UMR-S1250, SFR CAP-SANTE, Université de Reims Champagne-Ardenne, 51097, Reims, France.
Christine GillesGIGA-Cancer, Laboratory of Tumor and Development Biology, University of Liège, Liège, Belgium. cgilles@uliege.be.
University of Liège · BEInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial-mesenchymal transitions (EMTs) are high-profile in the field of circulating tumor cells (CTCs). EMT-shifted CTCs are considered to encompass pre-metastatic subpopulations though underlying molecular mechanisms remain elusive. Our previous work identified tissue factor (TF) as an EMT-induced gene providing tumor cells with coagulant properties and supporting metastatic colonization by CTCs. We here report that vimentin, the type III intermediate filament considered a canonical EMT marker, contributes to TF regulation and positively supports coagulant properties and early metastasis. Different evidence further pointed to a new post-transcriptional regulatory mechanism of TF mRNA by vimentin: (1) vimentin silencing accelerated TF mRNA decay after actinomycin D treatment, reflecting TF mRNA stabilization, (2) RNA immunoprecipitation revealed enriched levels of TF mRNA in vimentin immunoprecipitate, (3) TF 3'-UTR-luciferase reporter vector assays implicated the 3'-UTR of TF mRNA in vimentin-dependent TF regulation, and (4) using different TF 3'UTR-luciferase reporter vectors mutated for potential miR binding sites and specific Target Site Blockers identified a key miR binding site in vimentin-dependent TF mRNA regulation. All together, these data support a novel mechanism by which vimentin interferes with a miR-dependent negative regulation of TF mRNA, thereby promoting coagulant activity and early metastasis of vimentin-expressing CTCs.

Indexed as

3' Untranslated RegionsBreast NeoplasmsCell Line, TumorDactinomycinEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm MetastasisNeoplastic Cells, CirculatingRNA, MessengerRNA StabilityThromboplastinVimentin3' Untranslated RegionsDactinomycinMicroRNAsRNA, MessengerThromboplastinVimentin

Identifiers

PMID32152404
PMCPMC7190572
OpenAlexW3009615913

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.