Evidence map›Paper›PMID 35122963›Full record

ArticleMatrix biology : journal of the International Society for Matrix Biology2022

Coordination of two kinesin superfamily motor proteins, KIF3A and KIF13A, is essential for pericellular matrix degradation by membrane-type 1 matrix metalloproteinase (MT1-MMP) in cancer cells.

Valentina Gifford, Anna Woskowicz, Noriko Ito, Stefan Balint, B Christopher Lagerholm, Michael L Dustin, Yoshifumi Itoh

Open access · hybridAbstract read
In one paragraph

Article in Matrix biology : journal of the International Society for Matrix Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Matrix Metalloproteinase 14 in Corneal Neovascularization.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Article
  8. Article
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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

7 authors at 1 institution in 2 countries.

Valentina GiffordKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Anna WoskowiczKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Noriko ItoKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Stefan BalintKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
B Christopher LagerholmKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Michael L DustinKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Yoshifumi ItohKennedy Institute of Rheumatology, University of Oxford, Oxford, UK. Electronic address: yoshi.itoh@kennedy.ox.ac.uk.
University of Oxford · GB

Funding

Cancer Research UK C1507/A12015Wellcome TrustWellcome Trust 100262Z/12/Z
6 · The paper itself

Abstract

MT1-MMP plays a crucial role in promoting the cellular invasion of cancer cells by degrading the extracellular matrix to create a path for migration. During this process, its localization at the leading edge of migrating cells is critical, and it is achieved by targeted transport of MT1-MMP-containing vesicles along microtubules by kinesin superfamily motor proteins (KIFs). Here we identified three KIFs involved in MT1-MMP vesicle transport: KIF3A, KIF13A, and KIF9. Knockdown of KIF3A and KIF13A effectively inhibited MT1-MMP-dependent collagen degradation and invasion, while knockdown of KIF9 increased collagen degradation and invasion. Our data suggest that KIF3A/KIF13A dependent MT1-MMP vesicles transport takes over upon KIF9 knockdown. Live-cell imaging analyses have indicated that KIF3A and KIF13A coordinate to transport the same MT1-MMP-containing vesicles from the trans-Golgi to the endosomes, and KIF13A alone transports the vesicle from the endosome to the plasma membrane. Taken together, we have identified a unique interplay between three KIFs to regulate leading edge localization of MT1-MMP and MT1-MMP-dependent cancer cell invasion.

Indexed as

KinesinsMatrix Metalloproteinase 14Cell Line, TumorCell MovementEndosomesExtracellular MatrixHumansNeoplasm InvasivenessKIF13A protein, humanKIF3A protein, humanKinesinsMatrix Metalloproteinase 14Cancer invasionKIF13AKIF3AKIF9MT1-MMP

Identifiers

PMID35122963
PMCPMC9355896
OpenAlexW4210549754

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.