Evidence map›Paper›PMID 29393427›Full record

ArticleInternational journal of oncology2018

Plasma-stimulated medium kills TRAIL-resistant human malignant cells by promoting caspase-independent cell death via membrane potential and calcium dynamics modulation.

Tomohiko Tokunaga, Takashi Ando, Miki Suzuki-Karasaki, Tomohisa Ito, Asuka Onoe-Takahashi, Toyoko Ochiai, Masayoshi Soma, Yoshihiro Suzuki-Karasaki

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Cancer: A bioelectric disease?Clinical and translational medicine · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. The Role of Calcium Signaling in Melanoma.International journal of molecular sciences · 2022
    Review
  7. Review
  8. The Two-Way Relationship Between Calcium and Metabolism in Cancer.Frontiers in cell and developmental biology · 2020
    Review
  9. Article
  10. Article
  11. 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

8 authors at 2 institutions in 1 country.

Tomohiko TokunagaDivision of General Medicine, Nihon University School of Medicine, Tokyo 173-8610, Japan.
Takashi AndoDepartment of Orthopedic Surgery, Yamanashi University School of Medicine, Chuo, Yamanashi 409-3898, Japan.
Miki Suzuki-KarasakiPlasma ChemiBio Laboratory, Nasushiobara, Tochigi 329-2813, Japan.
Tomohisa ItoDepartment of Orthopedic Surgery, Nihon University School of Medicine, Tokyo 173-8610, Japan.
Asuka Onoe-TakahashiDepartment of Dermatology, Nihon University Hospital, Tokyo 101-8309, Japan.
Toyoko OchiaiDepartment of Dermatology, Nihon University Hospital, Tokyo 101-8309, Japan.
Masayoshi SomaDivision of General Medicine, Nihon University School of Medicine, Tokyo 173-8610, Japan.
Yoshihiro Suzuki-KarasakiPlasma ChemiBio Laboratory, Nasushiobara, Tochigi 329-2813, Japan.
Nihon University · JPUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and cold plasma-stimulated medium (PSM) have been shown to exhibit tumor-selective cytotoxicity and have emerged as promising new tools for cancer treatment. However, to date, at least to the best of our knowledge, no data are available as to which substance is more potent in killing cancer cells. Thus, in this study, we systematically compared their abilities to kill human malignant cells from different origins. We found that PSM dose-dependently killed TRAIL-resistant melanoma, osteosarcoma and neuroblastoma cells. Moreover, PSM had little cytotoxicity toward osteoblasts. PSM was more potent than TRAIL in inducing caspase-3/7 activation, mitochondrial network aberration and caspase-independent cell death. We also found that PSM was more potent in inducing plasma membrane depolarization (PMD) and disrupting endoplasmic-mitochondrial Ca2+ homeostasis. Moreover, persistent PMD was caused by different membrane-depolarizing agents; the use of the anti-type II diabetes drug, glibenclamide, alone caused mitochondrial fragmentation and enhanced TRAIL-induced Ca2+ modulation, mitochondrial network abnormalities and caspase-independent cell killing. These results demonstrate that PSM has a therapeutic advantage over TRAIL owing to its greater capacity to evoke caspase-independent cell death via mitochondrial network aberration by disrupting membrane potential and Ca2+ homeostasis. These findings may provide a strong rationale for developing PSM as a novel approach for the treatment of TRAIL-resistant malignant cells.

Indexed as

CalciumCaspase 3Caspase 7Cell DeathCell Line, TumorCulture MediaDose-Response Relationship, DrugDrug Resistance, NeoplasmGlyburideHumansMembrane Potential, MitochondrialMitochondriaMitochondrial MembranesNeoplasmsPlasma GasesRecombinant ProteinsCalciumCASP3 protein, humanCASP7 protein, humanCaspase 3Caspase 7Culture MediaGlyburidePlasma GasesRecombinant ProteinsTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, human

Identifiers

PMID29393427
PMCPMC5807047
OpenAlexW2788346797

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.