Mitochondrial-targeted nitroxides disrupt mitochondrial architecture and inhibit expression of peroxiredoxin 3 and FOXM1 in malignant mesothelioma cells.

Abstract

Malignant mesothelioma (MM) is an intractable tumor of the peritoneal and pleural cavities primarily linked to exposure to asbestos. Recently, we described an interplay between mitochondrial-derived oxidants and expression of FOXM1, a redox-responsive transcription factor that has emerged as a promising therapeutic target in solid malignancies. Here we have investigated the effects of nitroxides targeted to mitochondria via triphenylphosphonium (TPP) moieties on mitochondrial oxidant production, expression of FOXM1 and peroxiredoxin 3 (PRX3), and cell viability in MM cells in culture. Both Mito-carboxy-proxyl (MCP) and Mito-TEMPOL (MT) caused dose-dependent increases in mitochondrial oxidant production that was accompanied by inhibition of expression of FOXM1 and PRX3 and loss of cell viability. At equivalent concentrations TPP, CP, and TEMPOL had no effect on these endpoints. Live cell ratiometric imaging with a redox-responsive green fluorescent protein targeted to mitochondria (mito-roGFP) showed that MCP and MT, but not CP, TEMPOL, or TPP, rapidly induced mitochondrial fragmentation and swelling, morphological transitions that were associated with diminished ATP levels and increased production of mitochondrial oxidants. Mdivi-1, an inhibitor of mitochondrial fission, did not rescue mitochondria from fragmentation by MCP. Immunofluorescence microscopy experiments indicate a fraction of FOXM1 coexists in the cytoplasm with mitochondrial PRX3. Our results indicate that MCP and MT inhibit FOXM1 expression and MM tumor cell viability via perturbations in redox homeostasis caused by marked disruption of mitochondrial architecture, and suggest that both compounds, either alone or in combination with thiostrepton or other agents, may provide credible therapeutic options for the management of MM.

• Authors: Brian Cunniff, Kira Benson, Jason Stumpff, Kheng Newick, Paul Held, Douglas Taatjes, Joy Joseph, Balaraman Kalyanaraman, Nicholas H Heintz
• Journal: Journal of cellular physiology (J Cell Physiol) Vol. 228 Issue 4 Pg. 835-45 (Apr 2013) ISSN: 1097-4652 [Electronic] United States
• PMID: 23018647 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2012 Wiley Periodicals, Inc.

Chemical References

• 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone
• FOXM1 protein, human
• Forkhead Box Protein M1
• Forkhead Transcription Factors
• Organophosphorus Compounds
• Oxidants
• Quinazolinones
• triphenylphosphonium methylide
• Adenosine Triphosphate
• PRDX3 protein, human
• Peroxiredoxin III

Topics

• Adenosine Triphosphate (metabolism)
• Cell Line, Tumor
• Cell Survival (drug effects, genetics)
• Cytoplasm (drug effects, genetics, metabolism, physiology)
• Forkhead Box Protein M1
• Forkhead Transcription Factors (antagonists & inhibitors, biosynthesis, genetics, metabolism)
• Homeostasis (drug effects, genetics, physiology)
• Humans
• Mesothelioma (metabolism, pathology)
• Mitochondria (drug effects, metabolism)
• Mitochondrial Dynamics (drug effects, genetics, physiology)
• Organophosphorus Compounds (pharmacology)
• Oxidants (metabolism)
• Oxidation-Reduction (drug effects)
• Peroxiredoxin III (antagonists & inhibitors, biosynthesis, genetics, metabolism)
• Quinazolinones (pharmacology)