Pharmacological Ascorbic Acid and Hyperbaric Oxygen Therapy Target Tumor Cell Metabolism via an Oxidative Stress Mechanism
Poster Feb 15, 2017
Janine M. DeBlasi, Nathan P. Ward, PhD, Angela M. Poff, PhD, Andrew P. Koutnik, BS, Christopher Q. Rogers, PhD, David M. Diamond, PhD, Dominic P. D'Agostino, PhD
High-dose ascorbic acid (AA) is an anti-carcinogenic, minimally toxic, metabolic therapy that targets tumor cell metabolism via an oxidative stress (OxS) mechanism. At pharmacological levels (achieved i.v.), AA delivers H2O2 to tumorous tissue upon oxidation, initiating cell death. High-dose AA has shown significant anticancer effects in vitro, in vivo, and in small-scale human reports at concentrations nontoxic to normal cells, thus having great potential as an adjuvant to the standard of care. Hyperbaric oxygen therapy (HBOT) is another non-toxic, pro-oxidative, metabolic therapy that delivers 100% oxygen at elevated barometric pressure, elevating tissue pO2 and oxygenating hypoxic tumor cells, which, when coupled with high levels of reactive oxygen and nitrogen species present in cancer cells, can further augment OxS and lead to cell death. We hypothesized that AA would induce ROS-dependent OxS and that this would be further augmented with HBOT. This study’s aims were as follows (1) to examine the anticancer effect of AA in vitro, (2) to evaluate the mechanism of AA-induced OxS, (3) to determine if HBOT and AA are synergistic.
To characterize the anticancer effects of AA in vitro, we measured cell viability and proliferation following treatment with graded concentrations of AA in mouse brain tumor-derived VM-M3 cells. We found that AA mediates cell death in a concentration-dependent manner, and that concentrations great than or equal to 0.5mM AA significantly induced cell death compared to control. We also found that concentrations > 0.05mM AA inhibit cell proliferation compared to control and 0.01mM AA at 72 and 96 hours of growth. To investigate the role of OxS in AA-induced cytotoxicity, we measured VM-M3 cell viability in the presence of AA and antioxidant N-Acetylcysteine (NAC), and found that treatment with 0.5 and 5mM NAC attenuates the OxS-induced cytotoxic effect of AA. To determine if HBOT can enhance the therapeutic effect of AA, we measured VM-M3 cell viability following treatment with HBOT and AA. We found that HBOT significantly enhanced the cytotoxic effect of 0.3mM AA.
This data indicates that AA exhibits anti-cancer effects in vitro through an OxS mechanism and that HBOT can enhance this therapeutic effect. Evidence supports the use of these minimally toxic, pro-oxidative, metabolic therapies as adjuvants to the current standard of care.
Assessment of Oral LISPRO Treatment in Ameliorating Amyloid and Tau Pathology in Transgenic Alzheimer’s Mice ModelPoster
Ionic co-crystals of lithium salicylate with organic proline (LISPRO) showed better safety and pharmacokinetic profile of lithium in plasma and brain of wild-type and transgenic Alzheimer mice model compared to lithium salts.READ MORE
Is Oxford Nanopore Technology Ready for Clinical Diagnostics?Poster
Our objective is to validate diagnostic services using Oxford Nanopore’s Minion in the first instance and to evaluate the cost and performance compared to existing sequencing technology in areas such as tumour DNA sequencing (and circulating tumour DNA), virology, microbiology, genetics and HLA-typing.READ MORE
CiPA Phase 2 Study: validation of an automated microelectrode array (MEA) assay of hiPSC-derived cardiomyocyte electrophysiology for cardiac safety evaluationPoster
These results support the use of hSC-CM and MEA technology for preclinical assessment of proarrhythmic risk within the proposed CiPA paradigm, and, more generally, demonstrate that automation of the CM-MEA assay can achieve high reliability and throughput for cardiac risk assessment in vitro.READ MORE
Comments | 0 ADD COMMENT
EMBL Conference: European Conference of Life Science Funders and Foundations
Apr 19 - Apr 20, 2018
EMBL Course: Techniques for Mammary Gland Research
Mar 05 - Mar 09, 2018
EMBL Course: Target Engagement in Biology and Drug Discovery
Feb 19 - Feb 23, 2018