An omics approach to delineating the molecular mechanisms that underlie the biological effects of physical plasma

Author:

Gonzales Lou I. S. A.1ORCID,Qiao Jessica W.1ORCID,Buffier Aston W.1ORCID,Rogers Linda J.23ORCID,Suchowerska Natalka3ORCID,McKenzie David R.234ORCID,Kwan Ann H.14ORCID

Affiliation:

1. School of Life and Environmental Sciences, The University of Sydney, NSW 2006 1 , Australia

2. Arto Hardy Family Biomedical Innovation Hub, Chris O'Brien Lifehouse 2 , Camperdown, NSW 2050, Australia

3. VectorLAB, School of Physics, The University of Sydney 3 , NSW 2006, Australia

4. Sydney Nano Institute, The University of Sydney 4 , NSW 2006, Australia

Abstract

The use of physical plasma to treat cancer is an emerging field, and interest in its applications in oncology is increasing rapidly. Physical plasma can be used directly by aiming the plasma jet onto cells or tissue, or indirectly, where a plasma-treated solution is applied. A key scientific question is the mechanism by which physical plasma achieves selective killing of cancer over normal cells. Many studies have focused on specific pathways and mechanisms, such as apoptosis and oxidative stress, and the role of redox biology. However, over the past two decades, there has been a rise in omics, the systematic analysis of entire collections of molecules in a biological entity, enabling the discovery of the so-called “unknown unknowns.” For example, transcriptomics, epigenomics, proteomics, and metabolomics have helped to uncover molecular mechanisms behind the action of physical plasma, revealing critical pathways beyond those traditionally associated with cancer treatments. This review showcases a selection of omics and then summarizes the insights gained from these studies toward understanding the biological pathways and molecular mechanisms implicated in physical plasma treatment. Omics studies have revealed how reactive species generated by plasma treatment preferentially affect several critical cellular pathways in cancer cells, resulting in epigenetic, transcriptional, and post-translational changes that promote cell death. Finally, this review considers the outlook for omics in uncovering both synergies and antagonisms with other common cancer therapies, as well as in overcoming challenges in the clinical translation of physical plasma.

Funder

Chris O'brien Lifehouse/Baileys

Publisher

AIP Publishing

Subject

General Medicine

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