Curcumin inhibits proliferation of gastric cancer cells by impairing ATP-sensitive potassium channel opening

BACKGROUND: This study was aimed to investigate whether ATP-sensitive potassium channel (K(ATP)) is involved in curcumin’s anti-proliferative effects against gastric cancer. METHODS: In an in vitro study, gastric cancer cell line SGC-7901 was treated with curcumin at serial concentrations and co-administrated with the K(ATP) opener, diazoxide. The effect of curcumin and diazoxide on proliferation were assessed by MTT assay. Mitochondrial membrane potential (MMP) was studied by flow cytometry detection of rhodamine 123 staining. Apoptosis was evaluated by flow cytometry detection of Annexin V propidium iodide double staining. In an in vivo study, SGC-7901 cells were planted into nude mice as xenografts. Animals were treated with curcumin co-administered with diazoxide. Tumor volume and tumor weight were observed. RESULTS: Curcumin incubation significantly induced loss of MMP in SGC-7901 cells in a dose- dependent manner (P < 0.05); the cell apoptotic rate also dramatically increased after curcumin incubation in a dose-dependent manner (P < 0.05). After co-administration with diazoxide, however, we found that both the MMP-loss-inducing and the apoptosis-inducing effects of curcumin in SGC-7901 cells were significantly impaired (all P < 0.05). As a result, the proliferation of SGC-7901 cells was maintained by diazoxide treatment. CONCLUSIONS: Impaired mitoK(ATP) opening causes MMP loss, and is involved in curcumin-induced apoptosis in gastric cancer.