Evidence map›Paper›PMID 24632816›Full record

ArticlePloS one2014

The focal adhesion-localized CdGAP regulates matrix rigidity sensing and durotaxis.

Duncan B Wormer, Kevin A Davis, James H Henderson, Christopher E Turner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

33 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Directional Cell Migration Guided by a Strain Gradient.Small (Weinheim an der Bergstrasse, Germany) · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Fixing the GAP: The role of RhoGAPs in cancer.European journal of cell biology · 2022
    Review
  10. Mechanobiology of the female reproductive system.Reproductive medicine and biology · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Zyxin Is Involved in Fibroblast Rigidity Sensing and Durotaxis.Frontiers in cell and developmental biology · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Use Microfluidic Chips to Study the Phototaxis of Lung Cancer Cells.International journal of molecular sciences · 2019
    Article
  20. Mechanical Model for Durotactic Cell Migration.ACS biomaterials science & engineering · 2019
    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

4 authors at 2 institutions in 1 country.

Duncan B WormerDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, New York, United States of America.
Kevin A DavisSyracuse Biomaterials Institute, Syracuse University, Syracuse, New York, United States of America.
James H HendersonSyracuse Biomaterials Institute, Syracuse University, Syracuse, New York, United States of America.
Christopher E TurnerDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, New York, United States of America.
SUNY Upstate Medical University · USSyracuse University · US

Funding

STRUCTURE AND FUNCTION OF PAXILLINR01GM047607 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 1996 to 2017
$5.5M
Paxillin and Hic-5 in Coordination of Cancer Cell Invasion MechanismsR01CA163296 · NCI · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA163296NIGMS NIH HHS R01 GM047607
6 · The paper itself

Abstract

Motile cells are capable of sensing the stiffness of the surrounding extracellular matrix through integrin-mediated focal adhesions and migrate towards regions of higher rigidity in a process known as durotaxis. Durotaxis plays an important role in normal development and disease progression, including tumor invasion and metastasis. However, the signaling mechanisms underlying focal adhesion-mediated rigidity sensing and durotaxis are poorly understood. Utilizing matrix-coated polydimethylsiloxane gels to manipulate substrate compliance, we show that cdGAP, an adhesion-localized Rac1 and Cdc42 specific GTPase activating protein, is necessary for U2OS osteosarcoma cells to coordinate cell shape changes and migration as a function of extracellular matrix stiffness. CdGAP regulated rigidity-dependent motility by controlling membrane protrusion and adhesion dynamics, as well as by modulating Rac1 activity. CdGAP was also found to be necessary for U2OS cell durotaxis. Taken together, these data identify cdGAP as an important component of an integrin-mediated signaling pathway that senses and responds to mechanical cues in the extracellular matrix in order to coordinate directed cell motility.

Indexed as

Cell AdhesionCell MovementCell Line, TumorCell MembraneExtracellular MatrixFocal AdhesionsGTPase-Activating ProteinsHumansPhosphoproteinsrac1 GTP-Binding ProteinARHGAP31 protein, humanGTPase-Activating ProteinsPhosphoproteinsrac1 GTP-Binding Protein

Identifiers

PMID24632816
PMCPMC3954768
OpenAlexW1980193327

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.