The cancer cells (RGK-1) were more sensitive to acetic acid than the normal cells (RGM-1), and the human cancer cells (KATO III) were more sensitive than the rat cancer cells (RGK-1). Moreover, the anticancer

activity of acetic acid existed not only in the gastric cancer cells but also other types of cancer, such as mesothelioma (ACC-MESO1 and MSTO-211H cells). In general, the stomach tumor is resistant to HCl. Otherwise, the tumor growth could be inhibited by gastric acid. A recent study shows that the KATO III cells are highly resistant to the pH changes in the culture medium, that is, 90–100% cell viability from pH 7.5 to pH 5.5.[13] This is in line with the results of the present study showing that Ceritinib supplier the gastric cells could survive even in the culture medium at pH ≤ 1. In fact, when HC was added at 0.3% or 0.1% concentration, the cell survival rate

of gastric cells (RGK-1 or RGM-1) was 80–85%. Acetic acid, given at 0.1% concentration, induced the cell death (KATO III cells) by 41.7% at pH 6.8 in the culture medium. This might suggest that the acetic acid-induced cell death was a direct cytotoxic effect, which was independent of pH in the medium. The results of the present study are also in agreement with our previous studies showing that a local serosal or submucosal application of acetic acid (within 5 mm in diameter) was without effect on gastric pH but caused the gastric mucosal damage, leading to the formation of a deep ulcer within the area exposed to acetic acid.[1-5, 7] The molecular mechanism by which acetic Leukocyte receptor tyrosine kinase acid induces the cell death remains unclear. In the present study, fluorochrome-labeled Annexin V was not detected by selleck chemicals llc flow cytometry analysis in the acetic acid-treated KATO III cells (data

not shown), probably suggesting that apoptosis was not involved in the acetic acid-induced cell death. Further studies are needed to identify the cell death pathway induced by acetic acid. It is also unknown why the cancer cells, particularly the human cancer cells, were more sensitive to acetic acid treatment than the normal (rat gastric epithelial cancer) cells, although it has a great clinical implication. Previously, we have suggested that topical application of acetic acid may be used as a cytoreductive treatment of gastric cancer in patients through endoscopy or laparoscopy.[7] The present study provides further evidence to support this idea. Moreover, we may suggest using an intraperitoneal application of acetic acid (but not ethanol) alone or in combination with intraperitoneal chemotherapy for treatment of peritoneal cancer.[14-21] In the future, it will be of interest to test this idea in proper animal models by combining acetic acid with cisplatin, mitomycin-C, 5-FU, leucovorin, paclitaxel, S-1, doxorubicin, and irinotecan.[21-25] Malignant pleural mesothelioma is known to be resistant to chemotherapy, and several new treatment strategies have been suggested and tested in clinical trial.