Evidence map›Paper›PMID 26504170›Full record

ArticleThe Journal of cell biology2015

ARF6-JIP3/4 regulate endosomal tubules for MT1-MMP exocytosis in cancer invasion.

Valentina Marchesin, Antonio Castro-Castro, Catalina Lodillinsky, Alessia Castagnino, Joanna Cyrta, Hélène Bonsang-Kitzis, Laetitia Fuhrmann, Marie Irondelle, Elvira Infante, Guillaume Montagnac and 3 more

Abstract read
In one paragraph

Article in The Journal of cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

91 citing papers in PubMed, 144 citations in OpenAlex.

  1. Review
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  10. Involvement of kinesins in skeletal dysplasia: a review.American journal of physiology. Cell physiology · 2024
    Review
  11. Article
  12. Article
  13. Membrane trafficking alterations in breast cancer progression.Frontiers in cell and developmental biology · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Cytoplasmic Tail of MT1-MMP: A Hub of MT1-MMP Regulation and Function.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Valentina MarchesinPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France University Pierre et Marie Curie Paris 06, 75000 Paris, France.
Antonio Castro-CastroPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Catalina LodillinskyPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Alessia CastagninoPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Joanna CyrtaPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Hélène Bonsang-KitzisDepartment of Translational Research, Residual Tumor and Response to Treatment Laboratory, Institut Curie, 75248 Paris, France Institut National de la Sante et de la Recherche Médicale, Unite Mixte de Recherche 932 Immunity and Cancer, Institut Curie, 75248 Paris, France Department of Surgery, Institut Curie, 75248 Paris, France.
Laetitia FuhrmannDepartment of Pathology, Institut Curie, 75248 Paris, France.
Marie IrondellePSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Elvira InfantePSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Guillaume MontagnacPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France.
Fabien ReyalDepartment of Translational Research, Residual Tumor and Response to Treatment Laboratory, Institut Curie, 75248 Paris, France Institut National de la Sante et de la Recherche Médicale, Unite Mixte de Recherche 932 Immunity and Cancer, Institut Curie, 75248 Paris, France Department of Surgery, Institut Curie, 75248 Paris, France.
Anne Vincent-SalomonDepartment of Pathology, Institut Curie, 75248 Paris, France.
Philippe ChavrierPSL Research University, Institut Curie, 75248 Paris, France Membrane and Cytoskeleton Dynamics, Centre National de la Recherche Scientifique, Unite Mixte de Recherche 144, 75248 Paris, France philippe.chavrier@curie.fr.
Institut Curie · FRDynamique du noyau · FRUniversité Paris Sciences et Lettres · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invasion of cancer cells into collagen-rich extracellular matrix requires membrane-tethered membrane type 1-matrix metalloproteinase (MT1-MMP) as the key protease for collagen breakdown. Understanding how MT1-MMP is delivered to the surface of tumor cells is essential for cancer cell biology. In this study, we identify ARF6 together with c-Jun NH2-terminal kinase-interacting protein 3 and 4 (JIP3 and JIP4) effectors as critical regulators of this process. Silencing ARF6 or JIP3/JIP4 in breast tumor cells results in MT1-MMP endosome mispositioning and reduces MT1-MMP exocytosis and tumor cell invasion. JIPs are recruited by Wiskott-Aldrich syndrome protein and scar homologue (WASH) on MT1-MMP endosomes on which they recruit dynein-dynactin and kinesin-1. The interaction of plasma membrane ARF6 with endosomal JIPs coordinates dynactin-dynein and kinesin-1 activity in a tug-of-war mechanism, leading to MT1-MMP endosome tubulation and exocytosis. In addition, we find that ARF6, MT1-MMP, and kinesin-1 are up-regulated in high-grade triple-negative breast cancers. These data identify a critical ARF6-JIP-MT1-MMP-dynein-dynactin-kinesin-1 axis promoting an invasive phenotype of breast cancer cells.

Indexed as

Adaptor Proteins, Signal TransducingADP-Ribosylation Factor 6ADP-Ribosylation FactorsCollagenEndosomesExocytosisFemaleHEK293 CellsHumansKinesinsMatrix Metalloproteinase 14Microfilament ProteinsNeoplasm InvasivenessNerve Tissue ProteinsProtein TransportRNA InterferenceAdaptor Proteins, Signal TransducingADP-Ribosylation Factor 6ADP-Ribosylation FactorsARF6 protein, humanCollagenKIF3A protein, humanKIF5B protein, humanKinesinsMAPK8IP3 protein, humanMatrix Metalloproteinase 14Microfilament ProteinsMMP14 protein, humanNerve Tissue ProteinsRNA, Small InterferingSPAG9 protein, humanWASH protein, human

Identifiers

PMID26504170
PMCPMC4621834
OpenAlexW1856497061

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.