Evidence map›Paper›PMID 30816227›Full record

ArticleScientific reports2019

Protein tyrosine phosphatase 4A3 (PTP4A3/PRL-3) promotes the aggressiveness of human uveal melanoma through dephosphorylation of CRMP2.

Laura Duciel, Océane Anezo, Kalpana Mandal, Cécile Laurent, Nathalie Planque, Frédéric M Coquelle, David Gentien, Jean-Baptiste Manneville, Simon Saule

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. ZebrafishInternational journal of molecular sciences · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Targeting PRL phosphatases in hematological malignancies.Expert opinion on therapeutic targets · 2024
    Review
  7. Article
  8. Investigating the Role of DUSP4 in Uveal Melanoma.Translational vision science & technology · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review of PIP2 in Cellular Signaling, Functions and Diseases.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. A Review of MicroRNA in Uveal Melanoma.OncoTargets and therapy · 2020
    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

9 authors at 5 institutions in 2 countries.

Laura DucielInstitut Curie, PSL Research University, CNRS, INSERM, Orsay, France.
Océane AnezoInstitut Curie, PSL Research University, CNRS, INSERM, Orsay, France.
Kalpana MandalInstitute for Medicine and Engineering, University of Pennsylvania, Philadelphia, 19104, USA.
Cécile LaurentCALYM LYSARC Institut Carnot, Paris, France.ORCID 0000-0002-3022-2283
Nathalie PlanqueInstitut Curie, PSL Research University, CNRS, INSERM, Orsay, France.
Frédéric M CoquelleInstitut Curie, PSL Research University, CNRS, INSERM, Orsay, France.
David GentienInstitut Curie, PSL Research University, Translational Research Departement, Genomics Platform, Paris, France.
Jean-Baptiste MannevilleInstitut Curie, Paris Sciences and Letters Research University, CNRS, Paris, France.ORCID 0000-0002-8670-3940
Simon SauleInstitut Curie, PSL Research University, CNRS, INSERM, Orsay, France. simon.saule@curie.fr.
Université Paris-Sud · FRCentre National de la Recherche Scientifique · FRThe Lymphoma Academic Research Organisation · FRUniversité Paris Sciences et Lettres · FRUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uveal melanoma (UM) is an aggressive tumor in which approximately 50% of patients develop metastasis. Expression of the PTP4A3 gene, encoding a phosphatase, is predictive of poor patient survival. PTP4A3 expression in UM cells increases their migration in vitro and invasiveness in vivo. Here, we show that CRMP2 is mostly dephosphorylated on T514 in PTP4A3 expressing cells. We also demonstrate that inhibition of CRMP2 expression in UM cells expressing PTP4A3 increases their migration in vitro and invasiveness in vivo. This phenotype is accompanied by modifications of the actin microfilament network, with shortened filaments, whereas cells with a inactive mutant of the phosphatase do not show the same behavior. In addition, we showed that the cell cytoplasm becomes stiffer when CRMP2 is downregulated or PTP4A3 is expressed. Our results suggest that PTP4A3 acts upstream of CRMP2 in UM cells to enhance their migration and invasiveness and that a low level of CRMP2 in tumors is predictive of poor patient survival.

Indexed as

Actin CytoskeletonBiomarkers, TumorCell Line, TumorCell MovementHumansIntercellular Signaling Peptides and ProteinsLoss of Function MutationMelanomaNeoplasm ProteinsNerve Tissue ProteinsProtein Tyrosine PhosphatasesUveal NeoplasmsBiomarkers, Tumorcollapsin response mediator protein-2Intercellular Signaling Peptides and ProteinsNeoplasm ProteinsNerve Tissue ProteinsProtein Tyrosine PhosphatasesPTP4A3 protein, human

Identifiers

PMID30816227
PMCPMC6395723
OpenAlexW2919095449

What Socratic holds

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LicenceCC BY
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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 Socratic graph.