Evidence map›Paper›PMID 28467380›Full record

ArticleInternational journal of molecular sciences2017

Nanosecond-Pulsed DBD Plasma-Generated Reactive Oxygen Species Trigger Immunogenic Cell Death in A549 Lung Carcinoma Cells through Intracellular Oxidative Stress.

Abraham Lin, Billy Truong, Sohil Patel, Nagendra Kaushik, Eun Ha Choi, Gregory Fridman, Alexander Fridman, Vandana Miller

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 2 pooled it
19.5field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 2 syntheses or guidelines pooled it, 193 citations in OpenAlex.

  1. Pooled it
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31 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

8 authors at 2 institutions in 2 countries.

Abraham LinC. & J. Nyheim Plasma Institute, Drexel University, Philadelphia, PA 19104, USA. agl46@glink.drexel.edu.
Billy TruongC. & J. Nyheim Plasma Institute, Drexel University, Philadelphia, PA 19104, USA. billytruong2016@gmail.com.
Sohil PatelC. & J. Nyheim Plasma Institute, Drexel University, Philadelphia, PA 19104, USA. ssp82@drexel.edu.
Nagendra KaushikPlasma Bioscience Research Center, Kwangwoon University, Seoul 139791, Korea. kaushik.nagendra@gmail.com.
Eun Ha ChoiPlasma Bioscience Research Center, Kwangwoon University, Seoul 139791, Korea. ehchoi@kw.ac.kr.
Gregory FridmanC. & J. Nyheim Plasma Institute, Drexel University, Philadelphia, PA 19104, USA. gf33@drexel.edu.
Alexander FridmanC. & J. Nyheim Plasma Institute, Drexel University, Philadelphia, PA 19104, USA. af55@drexel.edu.
Vandana MillerC. & J. Nyheim Plasma Institute, Drexel University, Philadelphia, PA 19104, USA. vmiller@coe.drexel.edu.
Drexel University · USKwangwoon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel application for non-thermal plasma is the induction of immunogenic cancer cell death for cancer immunotherapy. Cells undergoing immunogenic death emit danger signals which facilitate anti-tumor immune responses. Although pathways leading to immunogenic cell death are not fully understood; oxidative stress is considered to be part of the underlying mechanism. Here; we studied the interaction between dielectric barrier discharge plasma and cancer cells for oxidative stress-mediated immunogenic cell death. We assessed changes to the intracellular oxidative environment after plasma treatment and correlated it to emission of two danger signals: surface-exposed calreticulin and secreted adenosine triphosphate. Plasma-generated reactive oxygen and charged species were recognized as the major effectors of immunogenic cell death. Chemical attenuators of intracellular reactive oxygen species successfully abrogated oxidative stress following plasma treatment and modulated the emission of surface-exposed calreticulin. Secreted danger signals from cells undergoing immunogenic death enhanced the anti-tumor activity of macrophages. This study demonstrated that plasma triggers immunogenic cell death through oxidative stress pathways and highlights its potential development for cancer immunotherapy.

Indexed as

A549 CellsAdenosine TriphosphateAnalysis of VarianceAntigen-Presenting CellsApoptosisCalreticulinElectric ConductivityElectrodesHumansImmunityImmunotherapyNeoplasmsOxidative StressPlasma GasesQuartzReactive Oxygen SpeciesAdenosine TriphosphateCalreticulinCALR protein, humanPlasma GasesQuartzReactive Oxygen Speciesadenosine triphosphatecalreticulincancer immunotherapyimmunogenic cell deathnanosecond-pulsed dielectric barrier dischargenon-thermal plasmaoxidative stressplasma immunotherapy

Identifiers

PMID28467380
PMCPMC5454879
OpenAlexW2611807792

What OpenQuestion holds

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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.