Abstract | AIM: In this study, we evaluated the carcinostatic effects of combined ascorbic acid (AsA) and a capacitive-resistive electric transfer (CRet) hyperthermic apparatus-induced hyperthermic treatment on Ehrlich ascites tumor (EAT) cells. MATERIALS AND METHODS: EAT cells were exposed to various AsA (0-10 mM) concentrations for 1 h; they subsequently underwent CRet treatment for 15 min at 42 °C. Cell viability was assessed by the WST-8 assay 24 h after the combined treatment. Reactive oxygen species involvement was evaluated using catalase and tempol; caspase-3/7 activation was determined by their fluorescent substrates; cell proliferation were estimated by time-lapse observation. The effect on the cell cycle was analyzed by flow cytometry. RESULTS: Combined AsA and CRet treatment synergistically suppressed cell viability compared with either treatment alone, and these synergistically carcinostatic effects were evident even at noncytotoxic concentrations of AsA alone (≤ 2 mM). The carcinostatic effects of combined AsA and CRet treatment were attenuated in a dose-dependent manner by catalase addition, but not by the superoxide anion radical scavenger tempol. Time-lapse observation revealed that combined AsA and CRet treatment activated caspase-3/7 at 10-24 h after treatment, accompanied by significant cell growth suppression. Cell cycle analysis revealed that the rate of sub-G1-phase (apoptotic) cells was drastically increased at 12 h and 24 h, and that the G2/M-phase cells gradually increased at 6-24 h after treatment. CONCLUSION: These results indicate that combined AsA and CRet treatment synergistically inhibits EAT cell growth through G2/M arrest and apoptosis induction via H2O2 generation at lower AsA concentrations; this carcinostatic effect cannot be exerted by AsA alone.
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Authors | Y Saitoh, T Yoshimoto, S Kato, N Miwa |
Journal | Experimental oncology
(Exp Oncol)
Vol. 37
Issue 2
Pg. 94-9
(Jun 2015)
ISSN: 2312-8852 [Electronic] Ukraine |
PMID | 26112934
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents
- Reactive Oxygen Species
- Ascorbic Acid
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Topics |
- Animals
- Antineoplastic Agents
(pharmacology)
- Apoptosis
- Ascorbic Acid
(pharmacology)
- Carcinoma, Ehrlich Tumor
(therapy)
- Cell Cycle Checkpoints
- Cell Line, Tumor
- Cell Proliferation
- Cell Survival
- Combined Modality Therapy
- Drug Screening Assays, Antitumor
- Hyperthermia, Induced
- Reactive Oxygen Species
(metabolism)
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