Non-Thermal Plasma, as a New Physicochemical Source, to Induce Redox Imbalance and Subsequent Cell Death in Liver Cancer Cell Lines
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
Academy of Sciences of the Czech Republic - Czech Republic
IN 00023001
Institute for Clinical and Experimental Medicine - Czech Republic
European Structural and Investment Funds - European Union
SOLID21 - CZ.02.1.01/0.0/0.0/16_019/0000760
Czech Ministry of Education, Youth and Sports - Czech Republic
FV10081
The Ministry of Industry and Trade - Czech Republic
PubMed
30790509
DOI
10.33594/000000009
Knihovny.cz E-resources
- Keywords
- Apoptosis, Non-thermal plasma, Oxidative stress, Reactive oxygen species, Stress resistance, p53,
- MeSH
- Cell Death drug effects MeSH
- Hep G2 Cells MeSH
- Down-Regulation drug effects MeSH
- Carcinoma, Hepatocellular drug therapy genetics metabolism pathology MeSH
- Humans MeSH
- Tumor Suppressor Protein p53 biosynthesis genetics MeSH
- Liver Neoplasms drug therapy genetics metabolism pathology MeSH
- Oxidation-Reduction drug effects MeSH
- Plasma Gases pharmacology MeSH
- Reactive Oxygen Species metabolism MeSH
- Gene Expression Regulation, Neoplastic drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Tumor Suppressor Protein p53 MeSH
- Plasma Gases MeSH
- Reactive Oxygen Species MeSH
- TP53 protein, human MeSH Browser
BACKGROUND/AIMS: Alteration of cancer cell redox status has been recognized as a promising therapeutic implication. In recent years, the emerged field of non-thermal plasma (NTP) has shown considerable promise in various biomedical applications, including cancer therapy. However, understanding the molecular mechanisms procuring cellular responses remains incomplete. Thus, the aim of this study was a rigorous biochemical analysis of interactions between NTP and liver cancer cells. METHODS: The concept was validated using three different cell lines. We provide several distinct lines of evidence to support our findings; we use various methods (epifluorescent and confocal microscopy, clonogenic and cytotoxicity assays, Western blotting, pharmacological inhibition studies, etc.). RESULTS: We assessed the influence of NTP on three human liver cancer cell lines (Huh7, Alexander and HepG2). NTP treatment resulted in higher anti-proliferative effect against Alexander and Huh7 relative to HepG2. Our data clearly showed that the NTP-mediated alternation of mitochondrial membrane potential and dynamics led to ROS-mediated apoptosis in Huh7 and Alexander cells. Interestingly, plasma treatment resulted in p53 down-regulation in Huh7 cells. High levels of Bcl-2 protein expression in HepG2 resulted in their resistance in response to oxidative stress- mediated by plasma. CONCLUSION: We show thoroughly time- and dose-dependent kinetics of ROS accumulation in HCC cells. Furthermore, we show nuclear compartmentalization of the superoxide anion triggered by NTP. NTP induced apoptotic death in Huh7 liver cancer cells via simultaneous downregulation of mutated p53, pSTAT1 and STAT1. Contrary, hydrogen peroxide treatment results in autophagic cell death. We disclosed detailed mechanisms of NTP-mediated alteration of redox signalling in liver cancer cells.
Institute for Clinical and Experimental Medicine Prague Czech Republic
Institute of Experimental Medicine of the Czech Academy of Sciences Prague Czech Republic
Institute of Physics of the Czech Academy of Sciences Prague Czech Republic
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