Evidence map›Paper›PMID 24753582›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Control of MT1-MMP transport by atypical PKC during breast-cancer progression.

Carine Rossé, Catalina Lodillinsky, Laetitia Fuhrmann, Maya Nourieh, Pedro Monteiro, Marie Irondelle, Emilie Lagoutte, Sophie Vacher, François Waharte, Perrine Paul-Gilloteaux and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Observational
  6. Article
  7. Article
  8. Cytoplasmic Tail of MT1-MMP: A Hub of MT1-MMP Regulation and Function.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Review
  11. A review of Dynamin 2 involvement in cancers highlights a promising therapeutic target.Journal of experimental & clinical cancer research : CR · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Invadopodia: clearing the way for cancer cell invasion.Annals of translational medicine · 2020
    Review
  19. Article
  20. 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

19 authors at 6 institutions in 3 countries.

Carine RosséResearch Center, Institut Curie, 75005 Paris, France.
Catalina Lodillinsky
Laetitia Fuhrmann
Maya Nourieh
Pedro Monteiro
Marie Irondelle
Emilie Lagoutte
Sophie Vacher
François Waharte
Perrine Paul-Gilloteaux
Maryse Romao
Lucie Sengmanivong
Mark Linch
Johan van Lint
Graça Raposo
Anne Vincent-Salomon
Ivan Bièche
Peter J Parker
Philippe Chavrier
Institut Curie · FRCentre National de la Recherche Scientifique · FRCancer Research UK · GBDynamique du noyau · FRInserm · FRKU Leuven · BE

Funding

Cancer Research UK 15683
6 · The paper itself

Abstract

Dissemination of carcinoma cells requires the pericellular degradation of the extracellular matrix, which is mediated by membrane type 1-matrix metalloproteinase (MT1-MMP). In this article, we report a co-up-regulation and colocalization of MT1-MMP and atypical protein kinase C iota (aPKCι) in hormone receptor-negative breast tumors in association with a higher risk of metastasis. Silencing of aPKC in invasive breast-tumor cell lines impaired the delivery of MT1-MMP from late endocytic storage compartments to the surface and inhibited matrix degradation and invasion. We provide evidence that aPKCι, in association with MT1-MMP-containing endosomes, phosphorylates cortactin, which is present in F-actin-rich puncta on MT1-MMP-positive endosomes and regulates cortactin association with the membrane scission protein dynamin-2. Thus, cell line-based observations and clinical data reveal the concerted activity of aPKC, cortactin, and dynamin-2, which control the trafficking of MT1-MMP from late endosome to the plasma membrane and play an important role in the invasive potential of breast-cancer cells.

Indexed as

AdenocarcinomaAdultAgedBiological Transport, ActiveBreast NeoplasmsCarcinoma, Ductal, BreastCell Line, TumorCortactinCytoplasmic GranulesDisease ProgressionDynamin IIEndosomesExtracellular MatrixFemaleHumansIsoenzymesCortactinCTTN protein, humanDynamin IIIsoenzymesMatrix Metalloproteinase 14MMP14 protein, humanProtein Kinase CProtein Kinase C-lambdaProtein Kinase C zetaRNA, MessengerRNA, NeoplasmRNA, Small Interferingactin cytoskeletonmembrane trafficMMP14multi-vesicular body

Identifiers

PMID24753582
PMCPMC4020077
OpenAlexW2166336683

What OpenQuestion holds

Textmetadata
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.