Evidence map›Paper›PMID 27215466›Full record

ArticleScientific reports2016

Engineering a 3D microfluidic culture platform for tumor-treating field application.

Andrea Pavesi, Giulia Adriani, Andy Tay, Majid Ebrahimi Warkiani, Wei Hseun Yeap, Siew Cheng Wong, Roger D Kamm

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 84 citations in OpenAlex.

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  8. Intervertebral Disc-on-a-Chip as AdvancedFrontiers in bioengineering and biotechnology · 2021
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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 at 6 institutions in 3 countries.

Andrea PavesiBiosym IRG, Singapore-MIT Alliance for Research and Technology, 1 Create Way, 138602 Singapore, Singapore.
Giulia AdrianiBiosym IRG, Singapore-MIT Alliance for Research and Technology, 1 Create Way, 138602 Singapore, Singapore.
Andy TayDepartment of Bioengineering, University of California, Los Angeles, CA 90025, USA.
Majid Ebrahimi WarkianiSchool of Mechanical and Manufacturing Engineering, Australian Centre for NanoMedicine, University of New South Wales, Sydney, Australia.
Wei Hseun YeapSingapore Immunology Network (SIgN), Agency for Science, Technology and Research, A*STAR, 8A Biomedical Grove, Immunos, Singapore 138648, Singapore.
Siew Cheng WongSingapore Immunology Network (SIgN), Agency for Science, Technology and Research, A*STAR, 8A Biomedical Grove, Immunos, Singapore 138648, Singapore.
Roger D KammBiosym IRG, Singapore-MIT Alliance for Research and Technology, 1 Create Way, 138602 Singapore, Singapore.
Singapore-MIT Alliance for Research and Technology · SGAgency for Science, Technology and Research · SGMassachusetts Institute of Technology · USNational University of Singapore · SGSingapore Immunology Network · SGUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The limitations of current cancer therapies highlight the urgent need for a more effective therapeutic strategy. One promising approach uses an alternating electric field; however, the mechanisms involved in the disruption of the cancer cell cycle as well as the potential adverse effects on non-cancerous cells must be clarified. In this study, we present a novel microfluidic device with embedded electrodes that enables the application of an alternating electric field therapy to cancer cells in a 3D extracellular matrix. To demonstrate the potential of our system to aid in designing and testing new therapeutic approaches, cancer cells and cancer cell aggregates were cultured individually or co-cultured with endothelial cells. The metastatic potential of the cancer cells was reduced after electric field treatment. Moreover, the proliferation rate of the treated cancer cells was lower compared with that of the untreated cells, whereas the morphologies and proliferative capacities of the endothelial cells were not significantly affected. These results demonstrate that our novel system can be used to rapidly screen the effect of an alternating electric field on cancer and normal cells within an in vivo-like microenvironment with the potential to optimize treatment protocols and evaluate synergies between tumor-treating field treatment and chemotherapy.

Indexed as

A549 CellsCell Line, TumorCell ProliferationCell SurvivalCoculture TechniquesElectric Stimulation TherapyEndothelial CellsEquipment DesignGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsMicrofluidic Analytical TechniquesNeoplasms

Identifiers

PMID27215466
PMCPMC4877588
OpenAlexW2407836966

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.