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DON 对胃癌细胞HGC-27 细胞周期和凋亡的影响[J]. 肿瘤防治研究, 2007, 34(12): 897-900. DOI: 10.3971/j.issn.1000-8578.65
引用本文: DON 对胃癌细胞HGC-27 细胞周期和凋亡的影响[J]. 肿瘤防治研究, 2007, 34(12): 897-900. DOI: 10.3971/j.issn.1000-8578.65
Effects of Deoxynivalenol on Cell Cycle and Apoptosis of Human Gastric Carcinoma Cell Line HGC-27 in vitro[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 897-900. DOI: 10.3971/j.issn.1000-8578.65
Citation: Effects of Deoxynivalenol on Cell Cycle and Apoptosis of Human Gastric Carcinoma Cell Line HGC-27 in vitro[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 897-900. DOI: 10.3971/j.issn.1000-8578.65

DON 对胃癌细胞HGC-27 细胞周期和凋亡的影响

Effects of Deoxynivalenol on Cell Cycle and Apoptosis of Human Gastric Carcinoma Cell Line HGC-27 in vitro

  • 摘要: 目的 探讨脱氧雪腐镰刀菌烯醇(DON)对体外培养胃癌细胞HGC-27细胞周期和凋亡的影响。方法 体外培养的胃癌细胞HGC-27经50、100、1000、2000μg/L DON处理12h、24h、48h,应用流式细胞术(FCM)进行细胞周期分析,检测凋亡情况及其量效关系,Western blot检测凋亡相关蛋白Bax、Bcl-2和Caspase-3的表达情况。结果 FCM检测结果表明,较高浓度(1000和2000μg/L)DON处理对细胞周期分布的影响随处理时间不同有明显差异。DON处理12h,可明显降低G0/G1细胞百分率、增加S期细胞百分率。处理时间延长至24h和48h,则表现为G0/G1细胞百分率增加,S期细胞百分率降低(P〈0.05)。DON处理24h和48h,各DON实验组HGC-27细胞凋亡率均高于对照组,在50~2000ug/L浓度范围内,凋亡率随着DON处理浓度的升高而升高。Western blot检测凋亡相关蛋白结果显示,DoN处理12、24和48h,Bax和Caspase-3蛋白表达均明显升高,而Bcl-2蛋白表达降低。结论 DON处理可影响体外培养的胃癌细胞象HGC-27细胞的细胞周期分布,其作用依DON浓度和作用时间的不同而有差异。同时DON可诱导HGC-27细胞凋亡,上调Bax和Caspase-3蛋白表达和下调Bcl-2蛋白表达可能是其诱导细胞凋亡的机制之一。

     

    Abstract: Objective  To explore the putative effect of deoxynivalenol on cell cycle and apoptosis of human gastric carcinoma cell line HGC-27 in vitro. Methods  HGC-27 cells were t reated with DON at different concent rations (50 、100 、1 000 、2 000μg/ L) for 12, 24 and 48 hours, and then cells were harvested for analysis of apoptosis, cell cycle dist ribution and expression of Bax, Bcl-2 and Caspase-3 with flow cytometric ( FCM) and Western Blot methods. Results  At relatively higher concent rations (1 000 and 2 000g/ L), DON could affect cell cycle dist ribution in a time dependent manner. DON treatment for 12 h, the percentages of cells in G0>>> / G1>>> phases was significantly decreased and that in S phase increased. As the treatment time lasted for 24 h and 48 h, the percentages of cells in G0>>> / G1>>>> phases were significantly increased while that in Sphase decreased ( P < 0. 05 ) . No significant effect s on G2 >>>/ M phase could be found. The apoptosis rates in all DON treated groups for 12 h, 24 h and 48 h were all higher than that in control. Though statistical significance in the difference of apoptosis rate between control and the DON treated groups was not found 12 h after DON treatment but it could be seen 24 and 48 h af ter DON treatment ( P < 0. 05) . Significant dose-effect relationships were found between DON concent rations and the apoptosis rates. Western Blot analysis showed bax and caspase-3 expression was up-regulated and bcl-2 expression was down-regulated in DON treated HGC-27 cells in vitro. Conclusion  DON could significantly affect the cell cycle distribution of HGC-27 cells in vitro and the effects of DON on cell cycle varied as the concentratrion and treatment time of DON changed. DON treatment could induce apoptosis of HGC-27 cell possibly by up-regulating bax and caspase-3 expression and down-regulating bcl-2 expression.

     

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