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Characterization of regulated cancer cell death pathways induced by the different modalities of non-thermal plasma
Eline Biscop1,2, Jana Baroen3,4, Joey De Backer5
1PLASMANT, Department of Chemistry, University of Antwerp, Antwerp, Belgium. eline.biscop@uantwerpen.be.
Abstract:
Non-thermal plasma (NTP) has shown promising anti-cancer effects, but there is still limited knowledge about the underlying cell death mechanisms induced by NTP and inherent differences between NTP treatment modalities. This study aimed to investigate four major regulated cell death (RCD) pathways, namely apoptosis, pyroptosis, necroptosis, and ferroptosis, in melanoma cancer cells following NTP treatment, and to provide an overview of molecular mechanistic differences between direct and indirect NTP treatment modalities. To discriminate which cell death pathways were triggered after treatment, specific inhibitors of apoptosis, pyroptosis, necroptosis, and ferroptosis were evaluated. RCD-specific molecular pathways were further investigated to validate the findings with inhibitors. Both direct and indirect NTP treatment increased caspase 3/7 and annexin V expression, indicative of apoptosis, as well as lipid peroxidation, characteristic of ferroptosis. Pyroptosis, on the other hand, was only induced by direct NTP treatment, evidenced by increased caspase 1 activity, whereas necroptosis was stimulated in a cell line-dependent manner. These findings highlight the molecular differences and implications of direct and indirect NTP treatment for cancer therapy. Altogether, activation of multiple cell death pathways offers advantages in minimizing treatment resistance and enhancing therapeutic efficacy, particularly in a combination setting. Understanding the mechanisms underlying NTP-induced RCD will enable the development of strategic combination therapies targeting multiple pathways to achieve cancer lethality.
Insights
Non-thermal plasma (NTP) triggers multiple cancer cell death pathways, including apoptosis and ferroptosis. Direct NTP uniquely induces pyroptosis, offering distinct therapeutic strategies for melanoma treatment.
Area of Science:
- Biomedical Engineering
- Cancer Biology
- Plasma Medicine
Background:
- Non-thermal plasma (NTP) demonstrates potential in anti-cancer therapies.
- Limited understanding exists regarding NTP-induced regulated cell death (RCD) mechanisms and treatment modality differences.
Purpose of the Study:
- To investigate apoptosis, pyroptosis, necroptosis, and ferroptosis in melanoma cells after NTP treatment.
- To delineate molecular mechanistic differences between direct and indirect NTP modalities.
Main Methods:
- Melanoma cells were treated with direct and indirect NTP.
- Specific inhibitors for apoptosis, pyroptosis, necroptosis, and ferroptosis were used to identify triggered RCD pathways.
- RCD-specific molecular markers (e.g., caspase activity, lipid peroxidation, annexin V) were analyzed.
Main Results:
- Both direct and indirect NTP induced apoptosis (increased caspase 3/7, annexin V) and ferroptosis (increased lipid peroxidation).
- Direct NTP uniquely triggered pyroptosis (increased caspase 1 activity).
- Necroptosis was induced in a cell line-dependent manner.
Conclusions:
- NTP activates multiple RCD pathways in melanoma cells, with distinct mechanisms for direct vs. indirect application.
- Understanding these RCD pathways is crucial for developing effective NTP-based cancer therapies.
- Targeting multiple pathways simultaneously via combination therapies can enhance therapeutic efficacy and overcome resistance.
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