Evidence map›Paper›PMID 26546985›Full record

ReviewExperimental cell research2016

Regulation of invadopodia by mechanical signaling.

Aron Parekh, Alissa M Weaver

Abstract readReview
In one paragraph

Review in Experimental cell research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

  1. Article
  2. Podosomes and Mechanical Force.Results and problems in cell differentiation · 2026
    Review
  3. Review
  4. Article
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  8. Article
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  15. Article
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  18. Article
  19. Dissemination of RasNature communications · 2020
    Article
  20. Invadopodia: clearing the way for cancer cell invasion.Annals of translational medicine · 2020
    Review
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

2 authors.

Aron ParekhDepartment of Otolaryngology, Vanderbilt University Medical Center, Nashville, TN 37232 USA; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN 37232 USA. Electronic address: aron.parekh@vanderbilt.edu.
Alissa M WeaverVanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN 37232 USA; Department of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN 37232 USA; Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232 USA; Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232 USA. Electronic address: alissa.weaver@vanderbilt.edu.

Funding

Multiscale Modeling of ECM-tumor interactions in Breast CancerU01CA143069 · NCI · VANDERBILT UNIVERSITY · PI JIANG, YI, KEELY, PATRICIA J · 2011 to 2015
$2.3M
Exocytic pathways in HNSCC progressionR01CA163592 · NCI · VANDERBILT UNIVERSITY · PI WEAVER, ALISSA M · 2012 to 2016
$1.6M
The Role of Basement Membrane Biomechanics in Cancer Cell InvasionK25CA143412 · NCI · VANDERBILT UNIVERSITY · PI PAREKH, ARON · 2010 to 2014
$572k
The Mechanical Phenotype of Fetal Fibroblasts as a Model for Regenerative RepairR03AR066875 · NIAMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PAREKH, ARON · 2015 to 2017
$236k
NCI NIH HHS K25 CA143412NCI NIH HHS R01 CA163592NCI NIH HHS U01 CA143069NIAMS NIH HHS R03 AR066875
6 · The paper itself

Abstract

Mechanical rigidity in the tumor microenvironment is associated with a high risk of tumor formation and aggressiveness. Adhesion-based signaling driven by a rigid microenvironment is thought to facilitate invasion and migration of cancer cells away from primary tumors. Proteolytic degradation of extracellular matrix (ECM) is a key component of this process and is mediated by subcellular actin-rich structures known as invadopodia. Both ECM rigidity and cellular traction stresses promote invadopodia formation and activity, suggesting a role for these structures in mechanosensing. The presence and activity of mechanosensitive adhesive and signaling components at invadopodia further indicates the potential for these structures to utilize myosin-dependent forces to probe and remodel their ECM environments. Here, we provide a brief review of the role of adhesion-based mechanical signaling in controlling invadopodia and invasive cancer behavior.

Indexed as

Mechanotransduction, CellularExtracellular MatrixHumansModels, BiologicalPodosomesTumor MicroenvironmentActinAdhesionContractilityExtracellular matrixInvadopodiaInvasionMechanotransductionProteinasesSecretionSignaling

Identifiers

PMID26546985
PMCPMC4851576

What OpenQuestion holds

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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.