Evidence map›Paper›PMID 40563685›Full record

ArticleCancers2025

Dual-Plasma Discharge Tube for Synergistic Glioblastoma Treatment.

William Murphy, Alex Horkowitz, Vikas Soni, Camil Walkiewicz-Yvon, Michael Keidar

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

William MurphyMicropropulsion and Nanotechnology Laboratory (MPNL), School of Engineering and Applied Science, George Washington University, 800 22nd St. NW, Suite 3100, Washington, DC 20052, USA.ORCID 0000-0001-9667-4445
Alex HorkowitzMicropropulsion and Nanotechnology Laboratory (MPNL), School of Engineering and Applied Science, George Washington University, 800 22nd St. NW, Suite 3100, Washington, DC 20052, USA.ORCID 0000-0002-7475-8450
Vikas SoniMicropropulsion and Nanotechnology Laboratory (MPNL), School of Engineering and Applied Science, George Washington University, 800 22nd St. NW, Suite 3100, Washington, DC 20052, USA.ORCID 0000-0002-0729-4641
Camil Walkiewicz-YvonMicropropulsion and Nanotechnology Laboratory (MPNL), School of Engineering and Applied Science, George Washington University, 800 22nd St. NW, Suite 3100, Washington, DC 20052, USA.
Michael KeidarMicropropulsion and Nanotechnology Laboratory (MPNL), School of Engineering and Applied Science, George Washington University, 800 22nd St. NW, Suite 3100, Washington, DC 20052, USA.ORCID 0000-0003-0869-4310

Funding

National Science Foundation 1747760
6 · The paper itself

Abstract

backgroundGlioblastoma (GBM) resists current therapies due to its rapid proliferation, diffuse invasion, and heterogeneous cell populations. We previously showed that a single cold atmospheric plasma discharge tube (DT) reduces GBM viability via broad-spectrum electromagnetic (EM) emissions. Here, we tested whether two DTs arranged in a helmet configuration could generate overlapping EM fields to amplify the anti-tumor effects without thermal injury.

methodsThe physical outputs of the single- and dual-DT setups were characterized by infrared thermography, broadband EM field probes, and oscilloscope analysis. Human U87-MG cells were exposed under the single or dual configurations. The viability was quantified with WST-8 assays mapped across 96-well plates; the intracellular reactive oxygen species (ROS), membrane integrity, apoptosis, and mitochondrial potential were assessed by multiparametric flow cytometry. Our additivity models compared the predicted versus observed dual-DT cytotoxicity.

resultsThe dual-DT operation produced constructive EM interference, elevating electric and magnetic field amplitudes over a broader area than either tube alone, while temperatures remained <39 °C. The single-DT exposure lowered the cell viability by ~40%; the dual-DT treatment reduced the viability by ~60%, exceeding the additive predictions. The regions of greatest cytotoxicity co-localized with the zones of highest EM field overlap. The dual-DT exposure doubled the intracellular ROS compared with single-DT and Annexin V positivity, confirming oxidative stress-driven cell death. The out-of-phase operation of the discharge tubes enabled the localized control of the treatment regions, which can guide future treatment planning.

conclusionsTwo synchronously operated plasma discharge tubes synergistically enhanced GBM cell killing through non-thermal mechanisms that coupled intensified overlapping EM fields with elevated oxidative stress. This positions modular multi-DT arrays as a potential non-invasive adjunct or alternative to existing electric-field-based therapies for glioblastoma.

Indexed as

cancercancer therapycold atmospheric plasmacold plasmadischarge tubeElectromagnetic field (non-invasive) therapyglioblastomanonthermal plasmaoncologyplasma

Identifiers

PMID40563685
PMCPMC12190360

What Socratic 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 Socratic graph.