Abstract
Transformed cells are subject to elimination through intercellular reactive oxygen/nitrogen species (RONS)-dependent apoptosis-inducing signaling. Tumor progression, therefore, requires expression of membrane-bound catalase. Recent research demonstrates that 1O2 can inactivate membrane-bound catalase, thus, inducing the generation of tumor cell-derived secondary 1O2 and RONS-dependent apoptosis selectively in tumor cells. Crucially, 1O2 signaling can result in self-perpetuating apoptotic signaling from cell-to-cell. It is known that CAP contains 1O2 and that certain CAP constituents can generate 1O2 in solution. The analysis of model experiments performed with defined RONS implies that CAP-derived 1O2 induces the mechanism through which CAP acts selectively against cancer cells in vitro and tumors in vivo. This hypothesis needs to be tested experimentally in order to establish its validity.
Original language | English (US) |
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Pages (from-to) | 1157-1178 |
Number of pages | 22 |
Journal | Plasma Processes and Polymers |
Volume | 13 |
Issue number | 12 |
DOIs | |
State | Published - Dec 1 2016 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Condensed Matter Physics
- Polymers and Plastics
Keywords
- catalase
- cold atmospheric plasma
- reactive oxygen/nitrogen species
- singlet oxygen
- tumor