Evidence map›Paper›PMID 24403990›Full record

ArticleBiomicrofluidics2013

Dielectrophoresis has broad applicability to marker-free isolation of tumor cells from blood by microfluidic systems.

Sangjo Shim, Katherine Stemke-Hale, Jamileh Noshari, Frederick F Becker, Peter R C Gascoyne

Abstract read
In one paragraph

Article in Biomicrofluidics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 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

5 authors.

Sangjo ShimDepartment of Imaging Physics Research, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA ; Department of Biomedical Engineering, The University of Texas at Austin, 1 University Station, C0800, Austin, Texas 78712, USA.
Katherine Stemke-HaleDepartment of Systems Biology, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Jamileh NoshariDepartment of Imaging Physics Research, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Frederick F BeckerDepartment of Molecular Pathology, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Peter R C GascoyneDepartment of Imaging Physics Research, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The number of circulating tumor cells (CTCs) found in blood is known to be a prognostic marker for recurrence of primary tumors, however, most current methods for isolating CTCs rely on cell surface markers that are not universally expressed by CTCs. Dielectrophoresis (DEP) can discriminate and manipulate cancer cells in microfluidic systems and has been proposed as a molecular marker-independent approach for isolating CTCs from blood. To investigate the potential applicability of DEP to different cancer types, the dielectric and density properties of the NCI-60 panel of tumor cell types have been measured by dielectrophoretic field-flow fractionation (DEP-FFF) and compared with like properties of the subpopulations of normal peripheral blood cells. We show that all of the NCI-60 cell types, regardless of tissue of origin, exhibit dielectric properties that facilitate their isolation from blood by DEP. Cell types derived from solid tumors that grew in adherent cultures exhibited dielectric properties that were strikingly different from those of peripheral blood cell subpopulations while leukemia-derived lines that grew in non-adherent cultures exhibited dielectric properties that were closer to those of peripheral blood cell types. Our results suggest that DEP methods have wide applicability for the surface-marker independent isolation of viable CTCs from blood as well as for the concentration of leukemia cells from blood.

Identifiers

PMID24403990
PMCPMC3562275

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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.