Evidence map›Paper›PMID 31635070›Full record

ArticleCancers2019

Cold Atmospheric Plasma-Treated PBS Eliminates Immunosuppressive Pancreatic Stellate Cells and Induces Immunogenic Cell Death of Pancreatic Cancer Cells.

Jinthe Van Loenhout, Tal Flieswasser, Laurie Freire Boullosa, Jorrit De Waele, Jonas Van Audenaerde, Elly Marcq, Julie Jacobs, Abraham Lin, Eva Lion, Heleen Dewitte and 6 more

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Targeting proteostasis pathways for cancer therapy.Journal of pharmaceutical analysis · 2025
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5 more citing papers are in PubMed but not listed here.

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

16 authors.

Jinthe Van LoenhoutCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. jinthe.vanloenhout@uantwerpen.be.ORCID 0000-0001-8576-5640
Tal FlieswasserCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. tal.flieswasser@uantwerpen.be.
Laurie Freire BoullosaCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. Laurie.freireboullosa@uantwerpen.be.
Jorrit De WaeleCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. jorrit.dewaele@uantwerpen.be.ORCID 0000-0002-9999-6156
Jonas Van AudenaerdeCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. jonas.vanaudenaerde@uantwerpen.be.ORCID 0000-0002-5619-1913
Elly MarcqCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. elly.marcq@uantwerpen.be.ORCID 0000-0003-3173-0500
Julie JacobsCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. julie.jacobs@uantwerpen.be.ORCID 0000-0003-2873-3364
Abraham LinCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. abraham.lin@uantwerpen.be.ORCID 0000-0003-0097-3323
Eva LionLaboratory of Experimental Hematology, University of Antwerp, 2610 Wilrijk, Belgium. eva.lion@uantwerpen.be.ORCID 0000-0002-2420-0301
Heleen DewitteLaboratory of General Biochemistry and Physical Pharmacy, Ghent University, 9000 Ghent, Belgium. heleen.dewitte@ugent.be.
Marc PeetersCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. marc.peeters@uza.be.
Sylvia DewildeProteinchemistry, proteomics and epigenetic signaling group, University of Antwerp, 2610 Wilrijk, Belgium. sylvia.dewilde@uantwerpen.be.
Filip LardonCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. filip.lardon@uantwerpen.be.ORCID 0000-0001-7174-4144
Annemie BogaertsPlasma, Laser Ablation and Surface Modelling Group, University of Antwerp, 2610 Wilrijk, Belgium. annemie.bogaerts@uantwerpen.be.ORCID 0000-0001-9875-6460
Christophe DebenCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. christophe.deben@uantwerpen.be.ORCID 0000-0001-8085-2040
Evelien SmitsCenter for Oncological Research, University of Antwerp, 2610 Wilrijk, Belgium. evelien.smits@uza.be.ORCID 0000-0001-9255-3435

Funding

Agentschap Innoveren en Ondernemen 141433Belgian group of Digestive Oncology NAFonds Wetenschappelijk Onderzoek 1121016NFonds Wetenschappelijk Onderzoek 11E7719NFonds Wetenschappelijk Onderzoek 12E3916NFonds Wetenschappelijk Onderzoek 12S9218NFonds Wetenschappelijk Onderzoek 1S32316NKom op tegen Kanker NAOlivia Hendrickx Research Fund NAStichting Tegen Kanker STK2014-155Universiteit Antwerpen NAVlaamse Vereniging voor Gastro-enterologie NA
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive cancers with a low response to treatment and a five-year survival rate below 5%. The ineffectiveness of treatment is partly because of an immunosuppressive tumor microenvironment, which comprises tumor-supportive pancreatic stellate cells (PSCs). Therefore, new therapeutic strategies are needed to tackle both the immunosuppressive PSC and pancreatic cancer cells (PCCs). Recently, physical cold atmospheric plasma consisting of reactive oxygen and nitrogen species has emerged as a novel treatment option for cancer. In this study, we investigated the cytotoxicity of plasma-treated phosphate-buffered saline (pPBS) using three PSC lines and four PCC lines and examined the immunogenicity of the induced cell death. We observed a decrease in the viability of PSC and PCC after pPBS treatment, with a higher efficacy in the latter. Two PCC lines expressed and released damage-associated molecular patterns characteristic of the induction of immunogenic cell death (ICD). In addition, pPBS-treated PCC were highly phagocytosed by dendritic cells (DCs), resulting in the maturation of DC. This indicates the high potential of pPBS to trigger ICD. In contrast, pPBS induced no ICD in PSC. In general, pPBS treatment of PCCs and PSCs created a more immunostimulatory secretion profile (higher TNF-α and IFN-γ, lower TGF-β) in coculture with DC. Altogether, these data show that plasma treatment via pPBS has the potential to induce ICD in PCCs and to reduce the immunosuppressive tumor microenvironment created by PSCs. Therefore, these data provide a strong experimental basis for further in vivo validation, which might potentially open the way for more successful combination strategies with immunotherapy for PDAC.

Indexed as

cold atmospheric plasmadendritic cellsimmunogenic cell deathpancreatic cancerpancreatic stellate cells

Identifiers

PMID31635070
PMCPMC6826654

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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.