Evidence map›Paper›PMID 31536516›Full record

ArticlePloS one2019

Characterization of sequentially-staged cancer cells using electrorotation.

Claudia I Trainito, Daniel C Sweeney, Jaka Čemažar, Eva M Schmelz, Olivier Français, Bruno Le Pioufle, Rafael V Davalos

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

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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

7 authors.

Claudia I TrainitoCNRS SATIE Institut d'Alembert ENS Paris Saclay, France.ORCID 0000-0002-2728-9364
Daniel C SweeneyDepartment of Biomedical Engineering and Mechanics, Virginia Tech, Blacksburg, Virginia, United States of America.ORCID 0000-0002-1289-1627
Jaka ČemažarDepartment of Biomedical Engineering and Mechanics, Virginia Tech, Blacksburg, Virginia, United States of America.
Eva M SchmelzDepartment of Human Nutrition, Food, and Exercise, Virginia Tech, Blacksburg, Virginia, United States of America.
Olivier FrançaisCNRS SATIE Institut d'Alembert ENS Paris Saclay, France.
Bruno Le PioufleCNRS SATIE Institut d'Alembert ENS Paris Saclay, France.
Rafael V DavalosDepartment of Biomedical Engineering and Mechanics, Virginia Tech, Blacksburg, Virginia, United States of America.

Funding

High-frequency Irreversible Electroporation (H-FIRE) combinatorial GBM treatmentR01CA213423 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI DAVALOS, RAFAEL VIDAL, VERBRIDGE, SCOTT S · 2017 to 2021
$1.7M
NCI NIH HHS R01 CA213423
6 · The paper itself

Abstract

The identification and separation of cells from heterogeneous populations is critical to the diagnosis of diseases. Label-free methodologies in particular have been developed to manipulate individual cells using properties such as density and morphology. The electrical properties of malignant cells, including the membrane capacitance and cytoplasmic conductivity, have been demonstrated to be altered compared to non-malignant cells of similar origin. Here, we exploit these changes to characterize individual cells in a sequentially-staged in vitro cancer model using electrorotation (EROT)-the rotation of a cell induced by a rotating electric field. Using a microfabricated device, a dielectrophoretic force to suspend cells while measuring their angular velocity resulting from an EROT force applied at frequencies between 3 kHz to 10 MHz. We experimentally determine the EROT response for cells at three stages of malignancy and analyze the resultant spectra by considering models that include the effect of the cell membrane alone (single-shell model) and the combined effect of the cell membrane and nucleus (double-shell model). We find that the cell membrane is largely responsible for a given cell's EROT response between 3 kHz and 10 MHz. Our results also indicate that membrane capacitance, membrane conductance, and cytoplasmic conductivity increase with an increasingly malignant phenotype. Our results demonstrate the potential of using electrorotation as a means making of non-invasive measurements to characterize the dielectric properties of cancer cells.

Indexed as

AnimalsCell Line, TumorCell MembraneCell SeparationElectric ConductivityElectrodesMiceModels, TheoreticalNeoplasmsNeoplasm StagingRotation

Identifiers

PMID31536516
PMCPMC6752768

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.