Evidence map›Paper›PMID 37287008›Full record

ArticleCancer cell international2023

Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation.

Austin R Smothers, Jason R Henderson, John J O'Connell, Jonathan M Stenbeck, Delphine Dean, Brian W Booth

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The therapeutic efficacy and application prospects of tumor-treating fields (TTFields) in resolving malignant tumors of central nervous system.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  5. Tumor-treating fields and concurrent cisplatin: anAmerican journal of cancer research · 2025
    Article
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 3 institutions in 1 country.

Austin R SmothersCenter for Innovative Medical Devices and Sensors (REDDI Lab), Clemson University, Clemson, SC, USA.
Jason R HendersonQuiverent LLC, Greenville, SC, USA.
John J O'ConnellPrisma Health Cancer Institute, Prisma Health, Greenville, SC, USA.
Jonathan M StenbeckPrisma Health Cancer Institute, Prisma Health, Greenville, SC, USA.
Delphine DeanCenter for Innovative Medical Devices and Sensors (REDDI Lab), Clemson University, Clemson, SC, USA.
Brian W BoothDepartment of Bioengineering, Clemson University, Clemson, SC, USA. brbooth@clemson.edu.ORCID http://orcid.org/0000-0003-2542-7302
Prisma Health · USSensors (United States) · USClemson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCurrently, tumor-treating field (TTField) therapy utilizes a single "optimal" frequency of electric fields to achieve maximal cell death in a targeted population of cells. However, because of differences in cell size, shape, and ploidy during mitosis, optimal electric field characteristics for universal maximal cell death may not exist. This study investigated the anti-mitotic effects of modulating electric field frequency as opposed to utilizing uniform electric fields.

methodsWe developed and validated a custom device that delivers a wide variety of electric field and treatment parameters including frequency modulation. We investigated the efficacy of frequency modulating tumor-treating fields on triple-negative breast cancer cells compared to human breast epithelial cells.

resultsWe show that frequency-modulated (FM) TTFields are as selective at treating triple-negative breast cancer (TNBC) as uniform TTFields while having a greater efficacy for combating TNBC cell growth. TTField treatment at a mean frequency of 150 kHz with a frequency range of ± 10 kHz induced apoptosis in a greater number of TNBC cells after 24 h as compared to unmodulated treatment which led to further decreased cell viability after 48 h. Furthermore, all TNBC cells died after 72 h of FM treatment while cells that received unmodulated treatment were able to recover to cell number equivalent to the control.

conclusionTTFields were highly efficacious against TNBC growth, FM TTFields showed minimal effects on epithelial cells similar to unmodulated treatment.

Indexed as

Breast cancerElectric field intensityFrequency modulationOscillating electric fieldsRadiotherapyTriple-negative breast cancer (TNBC)Tumor-treating fields (TTFields)

Identifiers

PMID37287008
PMCPMC10245511
OpenAlexW4379769411

What OpenQuestion holds

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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.