[Effects of deoxynivalenol on apoptosis of human gastric carcinoma cell line SGC-7901, BGC-823 in vitro].
Jing Liu, Xin Xing, Lingxiao Xing, Bingjuan Zhou
Abstract
Jing Liu, Xin Xing, Lingxiao Xing, Bingjuan Zhou
Abstract
OBJECTIVE: To explore the putative effects and possible mechanisms of deoxynivalenol (DON) on the apoptosis of human gastric carcinoma cell line SGC-7901, BGC-823 in vitro. METHODS: SGC-7901 and BGC-823 cells were treated with DON (50, 100, 1000 microg/L) for 72 hours, and then cells were harvested for the studies of apoptosis and the expression of Bax and Bcl-2 with flow cytometry (FCM), immunocytochemical staining and Western blot. RESULTS: FCM results showed that the apoptosis rates of SGC-7901 and BGC-823 cells in DON treatment groups were higher than that in control, and positive dose-effect correlations could be found in both cell lines (SGC-7901: r = 0.660, P < 0.05, n=4, BGC-823: r = 0.750, P < 0.01, n=4). FCM, immunocytochemical staining and Western blot results showed that the expression of Bax was increased while that of Bcl-2 was decreased in DON treatment groups of SGC-7901 and BGC-823. CONCLUSION: The results suggested that DON could induce apoptosis of SGC-7901, BGC-823 cells in vitro in a dose-dependent manner, and possible mechanisms may be increased formation of Bax-Bax homology dimer and decreased formationof Bax-Bcl-2 dimer by up-regulation of the expression of Bax and down-regulation of that Bcl-2.
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OBJECTIVE: To explore the putative effects and possible mechanisms of deoxynivalenol (DON) on the apoptosis of human gastric carcinoma cell line SGC-7901, BGC-823 in vitro. METHODS: SGC-7901 and BGC-823 cells were treated with DON (50, 100, 1000 microg/L) for 72 hours, and then cells were harvested for the studies of apoptosis and the expression of Bax and Bcl-2 with flow cytometry (FCM), immunocytochemical staining and Western blot. RESULTS: FCM results showed that the apoptosis rates of SGC-7901 and BGC-823 cells in DON treatment groups were higher than that in control, and positive dose-effect correlations could be found in both cell lines (SGC-7901: r = 0.660, P < 0.05, n=4, BGC-823: r = 0.750, P < 0.01, n=4). FCM, immunocytochemical staining and Western blot results showed that the expression of Bax was increased while that of Bcl-2 was decreased in DON treatment groups of SGC-7901 and BGC-823. CONCLUSION: The results suggested that DON could induce apoptosis of SGC-7901, BGC-823 cells in vitro in a dose-dependent manner, and possible mechanisms may be increased formation of Bax-Bax homology dimer and decreased formationof Bax-Bcl-2 dimer by up-regulation of the expression of Bax and down-regulation of that Bcl-2.
Key concepts: Apoptosis, Western blot, Flow cytometry, In vitro, Molecular biology, Cell culture, Cell, Staining