Acetic acid induces cell death: An in vitro study using normal rat gastric mucosal cell line and rat and human gastric cancer and mesothelioma cell lines

被引:14
|
作者
Okabe, Susumu [1 ,4 ]
Okamoto, Toshihiro [2 ]
Zhao, Chun-Mei [4 ]
Chen, Duan [4 ]
Matsui, Hirofumi [3 ]
机构
[1] Gen Corporat Assoc, Kyoto GI Dis Res Ctr, Kyoto 6048106, Japan
[2] Juntendo Univ, Grad Sch Med, Dept Therapy Dev & Innovat Immune Disorders & Can, Tokyo, Japan
[3] Univ Tsukuba, Div Gastroenterol, Tsukuba, Ibaraki, Japan
[4] Norwegian Univ Sci & Technol, Dept Canc Res & Mol Med, N-7034 Trondheim, Norway
关键词
acetic acid; KATO III cells; mesothelioma; RGK-1; cells; RGM-1; HYPERTHERMIC INTRAPERITONEAL CHEMOTHERAPY; NITRO-N-NITROSOGUANIDINE; OF-THE-ART; PERITONEAL CARCINOMATOSIS; MOUSE MODEL; EFFICACY; ULCER; PROTEIN;
D O I
10.1111/jgh.12775
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimWe recently reported that topical application of acetic acid promptly caused tumor necrosis in a mouse model of gastric cancer. The aim of the present study was to examine whether acetic acid can directly induce cancer cell death. MethodsRat gastric epithelial cell line (RGM-1), rat gastric carcinoma cell line (RGK-1), human gastric cancer cell line (KATO III), and human mesothelioma cell lines (ACC-MESO1 and MSTO-211H) were used. Acetic acid was added into the cell culture at different concentrations for different time periods. Cell death was analyzed by MTT assay, flow cytometry, and trypan blue exclusion test. ResultsAcetic acid promptly induced the cell death of RGM-1, RGK-1 cells, and KATO III cells in a concentration-dependent manner from 0.01% to 0.5%. Acetic acid at 0.5% for 1min induced the cell death by 80%. RGK-1 cells were more sensitive to acetic acid than RGM-l cells. KATO III cells were more sensitive to acetic acid than RGK-1 cells. Acetic acid at 0.5% for 10min induced almost complete cell death of ACC-MESO1 and MSTO-211H. ConclusionsAcetic acid is a powerful anticancer agent. Topical application of acetic acid may be a feasible approach for the treatments of gastric cancer and possibly other malignancies.
引用
收藏
页码:65 / 69
页数:5
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