Evidence map›Paper›PMID 31110227›Full record

ArticleScientific reports2019

Pulsed Electric Field Treatment Enhances the Cytotoxicity of Plasma-Activated Liquids in a Three-Dimensional Human Colorectal Cancer Cell Model.

Elena Griseti, Jelena Kolosnjaj-Tabi, Laure Gibot, Isabelle Fourquaux, Marie-Pierre Rols, Mohammed Yousfi, Nofel Merbahi, Muriel Golzio

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 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

8 authors.

Elena GrisetiCNRS UMR 5089, Institut de Pharmacologie et de Biologie Structurale, IPBS, 205 Route de Narbonne, 31077, Toulouse, France.
Jelena Kolosnjaj-TabiCNRS UMR 5089, Institut de Pharmacologie et de Biologie Structurale, IPBS, 205 Route de Narbonne, 31077, Toulouse, France.
Laure GibotCNRS UMR 5089, Institut de Pharmacologie et de Biologie Structurale, IPBS, 205 Route de Narbonne, 31077, Toulouse, France.
Isabelle FourquauxCentre de Microscopie Électronique Appliquée à la Biologie, CMEAB, 133 route de Narbonne Rangueil, 31062, Toulouse, Cedex, France.
Marie-Pierre RolsCNRS UMR 5089, Institut de Pharmacologie et de Biologie Structurale, IPBS, 205 Route de Narbonne, 31077, Toulouse, France.
Mohammed YousfiUniversité Toulouse III- Paul Sabatier, CNRS UMR 5213, Laboratoire des Plasmas et Conversion d'Énergie, LAPLACE, 118 Route de Narbonne-Bât 3R3-31062, Toulouse, France.
Nofel MerbahiUniversité Toulouse III- Paul Sabatier, CNRS UMR 5213, Laboratoire des Plasmas et Conversion d'Énergie, LAPLACE, 118 Route de Narbonne-Bât 3R3-31062, Toulouse, France. nofel.merbahi@laplace.univ-tlse.fr.
Muriel GolzioCNRS UMR 5089, Institut de Pharmacologie et de Biologie Structurale, IPBS, 205 Route de Narbonne, 31077, Toulouse, France. muriel.golzio@ipbs.fr.ORCID http://orcid.org/0000-0002-7470-3708

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cold atmospheric plasma and more recently, plasma-activated liquids (culture media, water or buffered solutions previously exposed to plasma), are gathering momentum in cancer cells treatment. Nevertheless, in vitro tests show that this novel approach is sometimes less efficient than expected. We here evaluate the mechanisms of action of the plasma-activated PBS and suggest to use electropermeabilization (EP) in combination with the plasma-activated phosphate-buffered saline (PBS), in order to potentiate the cytotoxic effect of the plasma activated liquid. Human multicellular tumor spheroids (MCTS), a three-dimensional cell model, which resembles small avascular tumors, was used to define the optimal treatment conditions for single and dual-mode treatments. MCTS growth, viability, and global morphological changes were assessed by live cell video-microscopy. In addition, the induction of caspases activation, the appearance of DNA damages, and cell membrane permeabilization, as well as the early modifications in the cellular ultrastructure, were examined by immunofluorescence, propidium iodide staining, confocal fluorescence microscopy and transmission electron microscopy, respectively. Altogether, our results show that a combined treatment resulted in an earlier onset of DNA damage and caspases activation, which completely abolished MCTS growth. This report is a proof of concept study evidencing that electropermeabilization greatly potentiates the cytotoxic effect of plasma-activated PBS in vitro in a three-dimensional cancer cell model.

Indexed as

Antineoplastic AgentsBuffersCell ProliferationColorectal NeoplasmsElectrochemotherapyHCT116 CellsHumansPlasma GasesSaline SolutionSpheroids, CellularAntineoplastic AgentsBuffersPlasma GasesSaline Solution

Identifiers

PMID31110227
PMCPMC6527570

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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.