Evidence map›Paper›PMID 23128389›Full record

ArticleOncogene2013

SLK-mediated phosphorylation of paxillin is required for focal adhesion turnover and cell migration.

J L Quizi, K Baron, K N Al-Zahrani, P O'Reilly, R K Sriram, J Conway, A-A Laurin, L A Sabourin

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PubMed Publisher
In one paragraph

Article in Oncogene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Biomolecules · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Ste20-like Kinase Is Critical for Inhibitory Synapse Maintenance and Its Deficiency Confers a Developmental Dendritopathy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Article
  11. Article
  12. The Journal of biological chemistry · 2019
    Article
  13. Article
  14. Ste20-like kinase, SLK, a novel mediator of podocyte integrity.American journal of physiology. Renal physiology · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

8 authors at 3 institutions in 1 country.

J L Quizi1] Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada [2] Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
K Baron
K N Al-Zahrani
P O'Reilly
R K Sriram
J Conway
A-A Laurin
L A Sabourin
University of Ottawa · CAOttawa Hospital · CAOttawa Hospital Research Institute

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Focal adhesion turnover is a complex process required for cell migration. We have previously shown that the Ste20-like kinase (SLK) is required for cell migration and efficient focal adhesion (FA) turnover in a FA kinase (FAK)-dependent manner. However, the role of SLK in this process remains unclear. Using a candidate substrate approach, we show that SLK phosphorylates the adhesion adapter protein paxillin on serine 250. Serine 250 phosphorylation is required for paxillin redistribution and cell motility. Mutation of paxillin serine 250 prevents its phosphorylation by SLK in vitro and results in impaired migration in vivo as evidenced by an accumulation of phospho-FAK-Tyr397 and altered FA turnover rates. Together, our data suggest that SLK phosphorylation of paxillin on serine 250 is required for FAK-dependent FA dynamics.

Indexed as

Protein Processing, Post-Translational3T3 CellsAmino Acid SequenceAnimalsCell MovementFocal AdhesionsHippo KinasesHumansMiceMolecular Sequence DataMutagenesis, Site-DirectedPaxillinPhosphorylationPhosphoserineProtein Serine-Threonine KinasesProtein Structure, TertiaryHippo KinasesPaxillinPhosphoserineProtein Serine-Threonine KinasesPXN protein, humanPxn protein, mouseRecombinant Fusion ProteinsSLK protein, humanSLK protein, mouse

Identifiers

PMID23128389
OpenAlexW2058777736

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.