Influence of hydrogen-occluding-silica on migration and apoptosis in human esophageal cells in vitro

• Published in: Medical gas research Vol. 7; no. 2; pp. 76 - 85
• Main Authors: Li, Qiang, Tanaka, Yoshiharu, Miwa, Nobuhiko
• Format: Journal Article
• Language: English
• Published: India Medknow Publications & Media Pvt. Ltd 01.04.2017; Medknow Publications & Media Pvt Ltd
• Subjects: Antioxidants; Apoptosis; Cancer therapies; Cell adhesion & migration; Chemical elements; Esophagus; Hydrogen; Laboratories; Oxidative stress; Penicillin; Potassium; Studies; Wound healing; United States > US; Japan; hydrogen-occluding-silica; car-cinogenic cells; apoptosis-inducing effect; reactive oxygen species; cell migration; cytotoxic effect; molecular hydrogen; normal human culture cells
• ISSN: 2045-9912; 2045-9912
• DOI: 10.4103/2045-9912.208510

In the last decade, many studies have shown that hydrogen gas or hydrogen water can reduce the levels of reactive oxygen species in the living body. Molecular hydrogen has antioxidant and antiapoptotic effects and a preventive effect on oxidative stress-induced cell death. In the present study, we investigated solidified hydrogen-occluding-silica (H -silica) that can release molecular hydrogen into cell culture medium because the use of hydrogen gas has strict handling limitations in hospital and medical facilities and laboratories, owing to its physicochemical characteristics. Human esophageal squamous cell carcinoma (KYSE-70) cells and normal human esophageal epithelial cells (HEEpiCs) were used to investigate the effects of H -silica on cell viability and proliferation. Cell migration was examined with wound healing and culture-insert migration assays. The intracellular levels of reactive oxygen species were evaluated with a nitroblue tetrazolium assay. To assess the apoptotic status of the cells, the Bax/Bcl-2 ratio and cleaved caspase-3 were analyzed by western blot. The results showed that KYSE-70 cells and HEEpiCs were generally inhibited by H -silica administration, and there was a significant proliferation-inhibitory effect in an H -silica concentration-dependent manner compared with the control group ( < 0.05) in KYSE-70. Apoptosis-inducing effect on KYSE-70 cells was observed in 10, 300, 600, and 1,200 ppm H -silica, and only 1,200 ppm H -silica caused a 2.4-fold increase in apoptosis in HEEpiCs compared with the control group as the index of Bax/Bcl-2. H silica inhibited cell migration in KYSE-70 cells, and high concentrations had a cytotoxic effect on normal cells. These findings should provide insights into the mechanism of inhibition of H -silica on human cancer cells .