Evidence map›Paper›PMID 25929519›Full record

ArticleBiomechanics and modeling in mechanobiology2015

Mechanical properties of normal versus cancerous breast cells.

Amanda M Smelser, Jed C Macosko, Adam P O'Dell, Scott Smyre, Keith Bonin, George Holzwarth

Open access · greenAbstract readComparative Study
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Amanda M SmelserDepartment of Biochemistry and Molecular Biology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Jed C MacoskoDepartment of Biochemistry and Molecular Biology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Adam P O'DellDepartment of Physics, Wake Forest University, Winston-Salem, NC, 27109, USA.
Scott SmyreDepartment of Physics, Wake Forest University, Winston-Salem, NC, 27109, USA.
Keith BoninDepartment of Physics, Wake Forest University, Winston-Salem, NC, 27109, USA.
George HolzwarthDepartment of Physics, Wake Forest University, Winston-Salem, NC, 27109, USA. gholz@wfu.edu.
Wake Forest University · US

Funding

Structural and Computational Biophysics Training ProgramT32GM095440 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOLLIS, THOMAS J, LYLES, DOUGLAS S. · 2011 to 2020
$1.7M
NIGMS NIH HHS T32 GM095440NIGMS NIH HHS T32GM095440
6 · The paper itself

Abstract

A cell's mechanical properties are important in determining its adhesion, migration, and response to the mechanical properties of its microenvironment and may help explain behavioral differences between normal and cancerous cells. Using fluorescently labeled peroxisomes as microrheological probes, the interior mechanical properties of normal breast cells were compared to a metastatic breast cell line, MDA-MB-231. To estimate the mechanical properties of cell cytoplasms from the motions of their peroxisomes, it was necessary to reduce the contribution of active cytoskeletal motions to peroxisome motion. This was done by treating the cells with blebbistatin, to inhibit myosin II, or with sodium azide and 2-deoxy-D-glucose, to reduce intracellular ATP. Using either treatment, the peroxisomes exhibited normal diffusion or subdiffusion, and their mean squared displacements (MSDs) showed that the MDA-MB-231 cells were significantly softer than normal cells. For these two cell types, peroxisome MSDs in treated and untreated cells converged at high frequencies, indicating that cytoskeletal structure was not altered by the drug treatment. The MSDs from ATP-depleted cells were analyzed by the generalized Stokes-Einstein relation to estimate the interior viscoelastic modulus G* and its components, the elastic shear modulus G' and viscous shear modulus G", at angular frequencies between 0.126 and 628 rad/s. These moduli are the material coefficients that enter into stress-strain relations and relaxation times in quantitative mechanical models such as the poroelastic model of the interior regions of cancerous and non-cancerous cells.

Indexed as

Models, BiologicalBreastBreast NeoplasmsCell AdhesionCell Line, TumorCell MovementComputer SimulationElastic ModulusHumansMechanotransduction, CellularMolecular Motor ProteinsPeroxisomesStress, MechanicalTensile StrengthTumor MicroenvironmentViscosityMolecular Motor ProteinsActinBrownian motionCytoskeletonGSEParticle trackingPeroxisomes

Identifiers

PMID25929519
PMCPMC4984850
OpenAlexW2013140880

What OpenQuestion holds

Textmetadata
LicenceTDM
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.