Evidence map›Paper›PMID 27383747›Full record

ArticleScientific reports2016

In-situ coupling between kinase activities and protein dynamics within single focal adhesions.

Yiqian Wu, Kaiwen Zhang, Jihye Seong, Jason Fan, Shu Chien, Yingxiao Wang, Shaoying Lu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Frontiers in physics · 2019
    Article
  9. Article
  10. Inositol hexakisphosphate kinase 3 promotes focal adhesion turnover via interactions with dynein intermediate chain 2.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. Article
  12. Focal adhesion kinase signaling in unexpected places.Current opinion in cell biology · 2017
    Review
  13. Soft matrices downregulate FAK activity to promote growth of tumor-repopulating cells.Biochemical and biophysical research communications · 2017
    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

7 authors at 2 institutions in 2 countries.

Yiqian WuDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Kaiwen ZhangDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Jihye SeongCenter for Neuro-Medicine, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.
Jason FanInstitute of Engineering in Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Shu ChienDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Yingxiao WangDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Shaoying LuDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
University of California San Diego · USKorean Association Of Science and Technology Studies · KR

Funding

Role of Spatiotemporal Epigenetic Dynamics in Regulating Endothelial Gene Expressions under FlowsR01HL121365 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIEN, SHU, WANG, YINGXIAO · 2014 to 2025
$7.5M
FRET Imaging of Molecular Hierarchy at Subcellular Levels in MechanotransductionR01HL098472 · NHLBI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI WANG, YINGXIAO · 2010 to 2014
$1.9M
The Integration of FLIM and FRET for the Visualization of Flow-induced MolecularK02HL109142 · NHLBI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI WANG, YINGXIAO · 2011 to 2015
$549k
NHLBI NIH HHS K02 HL109142NHLBI NIH HHS R01 HL098472NHLBI NIH HHS R01 HL121365
6 · The paper itself

Abstract

The dynamic activation of oncogenic kinases and regulation of focal adhesions (FAs) are crucial molecular events modulating cell adhesion in cancer metastasis. However, it remains unclear how these events are temporally coordinated at single FA sites. Therefore, we targeted fluorescence resonance energy transfer (FRET)-based biosensors toward subcellular FAs to report local molecular events during cancer cell adhesion. Employing single FA tracking and cross-correlation analysis, we quantified the dynamic coupling characteristics between biochemical kinase activities and structural FA within single FAs. We show that kinase activations and FA assembly are strongly and sequentially correlated, with the concurrent FA assembly and Src activation leading focal adhesion kinase (FAK) activation by 42.6 ± 12.6 sec. Strikingly, the temporal coupling between kinase activation and individual FA assembly reflects the fate of FAs at later stages. The FAs with a tight coupling tend to grow and mature, while the less coupled FAs likely disassemble. During FA disassembly, however, kinase activations lead the disassembly, with FAK being activated earlier than Src. Therefore, by integrating subcellularly targeted FRET biosensors and computational analysis, our study reveals intricate interplays between Src and FAK in regulating the dynamic life of single FAs in cancer cells.

Indexed as

Focal AdhesionsBinding SitesBiosensing TechniquesCell Line, TumorEnzyme ActivationFluorescence Resonance Energy TransferHumansProtein BindingProtein KinasesProteinsProtein KinasesProteins

Identifiers

PMID27383747
PMCPMC4935953
OpenAlexW2470496214

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.