Evidence map›Paper›PMID 31485083›Full record

ArticleJournal of physics D: Applied physics2019

Non-Thermal Plasma-Induced Immunogenic Cell Death in Cancer: A Topical Review.

Marian Khalili, Lynsey Daniels, Abraham Lin, Fred C Krebs, Adam E Snook, Sander Bekeschus, Wilbur B Bowne, Vandana Miller

Open access · bronzeAbstract read
In one paragraph

Article in Journal of physics D: Applied physics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 91 citations in OpenAlex.

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  19. Cold atmospheric plasma for addressing the COVID-19 pandemic.Plasma processes and polymers (Print) · 2022
    Review
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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 at 5 institutions in 3 countries.

Marian KhaliliDivision of Surgery Oncology, Department of Surgery, Drexel University College of Medicine, Philadelphia, PA.
Lynsey DanielsDivision of Surgery Oncology, Department of Surgery, Drexel University College of Medicine, Philadelphia, PA.
Abraham LinPlasma, Laser Ablation, and Surface Modeling (PLASMANT) Group, Department of Chemistry, University of Antwerp.
Fred C KrebsDepartment of Microbiology and Immunology, and Institute for Molecular Medicine &. Infectious Disease, Drexel University College of Medicine, Philadelphia, PA.
Adam E SnookDepartment of Pharmacology and Experimental Therapeutics, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.
Sander BekeschusCentre for Innovation Competence (ZIK) plasmatis, Leibniz Institute for Plasma Science and Technology (INP Greifswald), Felix-Hausdorff-Str.2, 17489 Greifswald, Germany.
Wilbur B BowneDivision of Surgery Oncology, Department of Surgery, Drexel University College of Medicine, Philadelphia, PA.
Vandana MillerDivision of Surgery Oncology, Department of Surgery, Drexel University College of Medicine, Philadelphia, PA.
Drexel University · USLeibniz Institute for Plasma Science and Technology · DEInstitute for Molecular Medicine · USThomas Jefferson University · USUniversity of Antwerp · BE

Funding

(PQ1) GUCY2C hormone loss translates APC-Beta-catenin mutations into epithelial transformationR01CA206026 · NCI · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA206026
6 · The paper itself

Abstract

Recent advances in biomedical research in cancer immunotherapy have identified the use of an oxidative stress-based approach to treat cancers, which works by inducing immunogenic cell death (ICD) in cancer cells. Since the anti-cancer effects of non-thermal plasma (NTP) are largely attributed to the reactive oxygen and nitrogen species that are delivered to and generated inside the target cancer cells, it is reasonable to postulate that NTP would be an effective modality for ICD induction. NTP treatment of tumors has been shown to destroy cancer cells rapidly and, under specific treatment regimens, this leads to systemic tumor-specific immunity. The translational benefit of NTP for treatment of cancer relies on its ability to enhance the interactions between NTP-exposed tumor cells and local immune cells which initiates subsequent protective immune responses. This review discusses results from recent investigations of NTP application to induce immunogenic cell death in cancer cells. With further optimization of clinical devices and treatment protocols, NTP can become an essential part of the therapeutic armament against cancer.

Identifiers

PMID31485083
PMCPMC6726388
OpenAlexW2977397672

What OpenQuestion holds

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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.