Evidence map›Paper›PMID 32438553›Full record

ArticleCancers2020

Cold-Atmospheric Plasma Induces Tumor Cell Death in Preclinical In Vivo and In Vitro Models of Human Cholangiocarcinoma.

Javier Vaquero, Florian Judée, Marie Vallette, Henri Decauchy, Ander Arbelaiz, Lynda Aoudjehane, Olivier Scatton, Ester Gonzalez-Sanchez, Fatiha Merabtene, Jérémy Augustin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
4.8field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 2 institutions in 3 countries.

Javier VaqueroInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.ORCID 0000-0002-6020-6962
Florian JudéeLPP (Laboratoire de physique des plasmas, UMR 7648), Sorbonne Université, Centre national de la recherche scientifique (CNRS), Ecole Polytechnique, 75005 Paris, France.
Marie ValletteInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Henri DecauchyLPP (Laboratoire de physique des plasmas, UMR 7648), Sorbonne Université, Centre national de la recherche scientifique (CNRS), Ecole Polytechnique, 75005 Paris, France.
Ander ArbelaizInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Lynda AoudjehaneInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Olivier ScattonInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Ester Gonzalez-SanchezInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Fatiha MerabteneInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Jérémy AugustinInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.ORCID 0000-0001-8194-0624
Chantal HoussetInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.
Thierry DufourLPP (Laboratoire de physique des plasmas, UMR 7648), Sorbonne Université, Centre national de la recherche scientifique (CNRS), Ecole Polytechnique, 75005 Paris, France.
Laura FouassierInstitut national de la santé et de la recherche médicale (Inserm), Centre de recherche Saint-Antoine, CRSA, Sorbonne Université, 75012 Paris, France.ORCID 0000-0001-6377-5610
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

Agence Nationale de la Recherche ANR-11-IDEX-0004-02Agence Nationale de la Recherche ANR-17-CE14-0013-01CANCEROPOLE ILE DE FRANCE 193602Fondation pour la Recherche Médicale FRM SPF201809007054Sésame Ile de France : PF2-ABIOMEDE 16016309Siric Curamus 195741Université Sorbonne Paris Cité 156815
6 · The paper itself

Abstract

Through the last decade, cold atmospheric plasma (CAP) has emerged as an innovative therapeutic option for cancer treatment. Recently, we have set up a potentially safe atmospheric pressure plasma jet device that displays antitumoral properties in a preclinical model of cholangiocarcinoma (CCA), a rare and very aggressive cancer emerging from the biliary tree with few efficient treatments. In the present study, we aimed at deciphering the molecular mechanisms underlying the antitumor effects of CAP towards CCA in both an in vivo and in vitro context. In vivo, using subcutaneous xenografts into immunocompromised mice, CAP treatment of CCA induced DNA lesions and tumor cell apoptosis, as evaluated by 8-oxoguanine and cleaved caspase-3 immunohistochemistry, respectively. The analysis of the tumor microenvironment showed changes in markers related to macrophage polarization. In vitro, the incubation of CCA cells with CAP-treated culture media (i.e., plasma-activated media, PAM) led to a dose response decrease in cell survival. At molecular level, CAP treatment induced double-strand DNA breaks, followed by an increased phosphorylation and activation of the cell cycle master regulators CHK1 and p53, leading to cell cycle arrest and cell death by apoptosis. In conclusion, CAP is a novel therapeutic option to consider for CCA in the future.

Indexed as

cholangiocarcinomacold plasmainnovative therapymacrophagesplasma jetplasma selectivitytumor cells

Identifiers

PMID32438553
PMCPMC7281400
OpenAlexW3026492047

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.