Evidence map›Paper›PMID 21281571›Full record

ArticleBiophysical journal2011

Sensing and modulation of invadopodia across a wide range of rigidities.

Aron Parekh, Nazanin S Ruppender, Kevin M Branch, M K Sewell-Loftin, Jun Lin, Patrick D Boyer, Joseph E Candiello, W David Merryman, Scott A Guelcher, Alissa M Weaver

Abstract read
In one paragraph

Article in Biophysical journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing 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

66 citing papers in PubMed.

  1. Article
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  3. Organoids technology in cancer research: from basic applications to advancedFrontiers in cell and developmental biology · 2025
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  20. Review

6 more citing papers are in PubMed but not listed here.

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

10 authors.

Aron ParekhDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, Tennesee.
Nazanin S RuppenderDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee.
Kevin M BranchDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, Tennesee.
M K Sewell-LoftinDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.
Jun LinDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee.
Patrick D BoyerDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee.
Joseph E CandielloDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
W David MerrymanDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.
Scott A GuelcherDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee.
Alissa M WeaverDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, Tennesee; Department of Pathology, Vanderbilt University Medical Center, Nashville, Tennesee. Electronic address: alissa.weaver@vanderbilt.edu.

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jin Chen · 1995 to 2026
$172.8M
TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI POWERS, ALVIN C · 1986 to 2011
$28.1M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Kevin L Schey · 1989 to 2026
$19.6M
TrainingU54CA113007 · NCI · VANDERBILT UNIVERSITY · PI ESTRADA-RODGERS, LOURDES · 2004 to 2014
$19.2M
THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
Cortactin function in lamellipodial protrusionR01GM075126 · NIGMS · VANDERBILT UNIVERSITY · PI WEAVER, ALISSA M · 2007 to 2011
$1.4M
TGF-beta1 activity in the aortic valveK25HL094707 · NHLBI · VANDERBILT UNIVERSITY · PI MERRYMAN, WILLIAM D · 2009 to 2013
$725k
NCI NIH HHS 1K25CA143412NCI NIH HHS 2P50 CA098131-06NCI NIH HHS 5P30 CA068485NCI NIH HHS CA68485NCI NIH HHS K25 CA143412NCI NIH HHS P30 CA068485NCI NIH HHS P50 CA098131NCI NIH HHS U54 CA113007NCI NIH HHS U54CA113007NEI NIH HHS EY08126NEI NIH HHS P30 EY008126NHLBI NIH HHS HL094707NHLBI NIH HHS K25 HL094707NICHD NIH HHS HD15052NICHD NIH HHS P30 HD015052NIDDK NIH HHS DK20593NIDDK NIH HHS DK58404NIDDK NIH HHS DK59637NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS P60 DK020593NIDDK NIH HHS U24 DK059637NIGMS NIH HHS 1R01GM075126NIGMS NIH HHS R01 GM075126
6 · The paper itself

Abstract

Recent studies have suggested that extracellular matrix rigidity regulates cancer invasiveness, including the formation of cellular invadopodial protrusions; however, the relevant mechanical range is unclear. Here, we used a combined analysis of tissue-derived model basement membrane (BM) and stromal matrices and synthetic materials to understand how substrate rigidity regulates invadopodia. Urinary bladder matrix-BM (UBM-BM) was found to be a rigid material with elastic moduli of 3-8 MPa, as measured by atomic force microscopy and low-strain tensile testing. Stromal elastic moduli were ∼6-fold lower, indicating a more compliant material. Using synthetic substrates that span kPa-GPa moduli, we found a peak of invadopodia-associated extracellular matrix degradation centered around 30 kPa, which also corresponded to a peak in invadopodia/cell. Surprisingly, we observed another peak in invadopodia numbers at 2 GPa as well as gene expression changes that indicate cellular sensing of very high moduli. Based on the measured elastic moduli of model stroma and BM, we expected to find more invadopodia formation on the stroma, and this was verified on the stromal versus BM side of UBM-BM. These data suggest that cells can sense a wide range of rigidities, up into the GPa range. Furthermore, there is an optimal rigidity range for invadopodia activity that may be limited by BM rigidity.

Indexed as

Acrylic ResinsAnimalsBasement MembraneBiomechanical PhenomenaCell Surface ExtensionsElastic ModulusExtracellular MatrixMicroscopy, Atomic ForceModels, BiologicalPolyacrylamidesPolyurethanesPressureSus scrofaUrinary BladderAcrylic ResinsPolyacrylamidesPolyurethanes

Identifiers

PMID21281571
PMCPMC3030182

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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.