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Basic Research in Plasma Medicine - A Throughput Approach from Liquids to Cells
Published on: November 17, 2017
Effect of atmospheric gas plasmas on cancer cell signaling
Musarat Ishaq1, Margaret Meg Evans, Kostya Ken Ostrikov
1Plasma Nanomedicine CSIRO Materials Science and Engineering, North Ryde, PO Box 52, NSW 1670, Australia; Plasma Nanoscience, CSIRO Materials Science and Engineering, PO Box 218, Lindfield 2070, NSW, Australia.
Abstract:
Cancer is one of the most life-threatening diseases with many forms still regarded as incurable. The conventional cancer treatments have unwanted side effects such as the death of normal cells. A therapy that can accurately target and effectively kill tumor cells could address the inadequacies of the available therapies. Atmospheric gas plasmas (AGP) that are able to specifically kill cancerous cells offer a promising alternative approach compared to conventional therapies. AGP have been shown to exploit tumor-specific genetic defects and a recent trial in mice has confirmed its antitumor effects. The mechanism by which the AGP act on tumor cells but not normal cells is not fully understood. A review of the current literature suggests that reactive oxygen species (ROS) generated by AGP induce death of cancer cells by impairing the function of intracellular regulatory factors. The majority of cancer cells are defective in tumor suppressors that interfere normal cell growth pathways. It appears that pro-oncogene or tumor suppressor-dependent regulation of antioxidant/or ROS signaling pathways may be involved in AGP-induced cancer cell death. The toxic effects of ROS are mitigated by normal cells by adjustment of their metabolic pathways. On the other hand, tumor cells are mostly defective in several regulatory signaling pathways which lead to the loss of metabolic balance within the cells and consequently, the regulation of cell growth. This review article evaluates the impact of AGP on the activation of cellular signaling and its importance for exploring mechanisms for safe and efficient anticancer therapies.
Insights
Atmospheric gas plasmas (AGP) offer a promising cancer therapy by selectively killing tumor cells. AGP-induced reactive oxygen species (ROS) exploit cancer cell defects, leading to cell death.
Area of Science:
- Biomedical Engineering
- Oncology
- Plasma Physics
Background:
- Conventional cancer treatments cause significant side effects due to non-specific cell killing.
- Atmospheric gas plasmas (AGP) present a novel therapeutic approach with demonstrated tumor-specific effects in preclinical models.
- The precise mechanisms underlying AGP's selective cancer cell toxicity remain incompletely understood.
Purpose of the Study:
- To review the current literature on the impact of AGP on cancer cells.
- To elucidate the role of reactive oxygen species (ROS) in AGP-induced cancer cell death.
- To explore the potential of AGP as a safe and effective anticancer therapy by understanding its cellular signaling mechanisms.
Main Methods:
- Literature review of existing studies on atmospheric gas plasmas and cancer therapy.
- Analysis of proposed mechanisms involving reactive oxygen species (ROS) and cellular signaling pathways.
- Evaluation of the differential effects of ROS on normal versus cancerous cells.
Main Results:
- AGP generates reactive oxygen species (ROS) that induce cancer cell death by disrupting intracellular regulatory factors.
- Cancer cells, often deficient in tumor suppressors, exhibit impaired ROS signaling pathway regulation.
- Normal cells can mitigate ROS toxicity through metabolic adjustments, unlike many cancer cells.
Conclusions:
- AGP therapy shows potential for selective cancer cell killing, exploiting tumor-specific genetic defects.
- Understanding the interplay between ROS, cellular signaling, and metabolic pathways is crucial for optimizing AGP anticancer efficacy.
- AGP represents a promising avenue for developing safer and more effective cancer treatments.
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