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作 者:桑建荣[1] 陈永昌[1] 邵根宝[2] 黄晓佳[3]
机构地区:[1]江苏大学基础医学与医学技术学院生理学系,镇江212013 [2]江苏大学基础医学与医学技术学院生物学系,镇江212013 [3]江苏大学基础医学与医学技术学院药理学系,镇江212013
出 处:《肿瘤》2010年第1期21-25,共5页Tumor
基 金:江苏大学高级专业人才科研启动基金资助项目(编号:08JDG033)
摘 要:目的:探讨外源一氧化氮(nitric oxide,NO)对胃癌细胞生长和增殖的影响。方法:应用MTT法评价NO供体硝普钠(sodium nitroprusside,SNP)和一氧化氮合酶(nitric oxide synthase,NOS)抑制剂N-硝基-L-精氨酸甲酯(N-nitro-L-argininemethylester,L-NAME)对胃癌SGC-7901细胞生长的抑制作用,RT-PCR和Western印迹法检测增殖细胞核抗原(proliferating cellnuclear antigen,PCNA)和Caspase-3 mRNA和蛋白的表达,FCM法检测细胞周期的变化。结果:SNP使细胞周期发生变化,与对照组比较,S期细胞减少,G0/G1期细胞增多,细胞由G0/G1期进入S期延缓;SNP抑制SGC-7901细胞的生长,PCNA mRNA、PCNA蛋白和Caspase-3蛋白表达降低。而NOS抑制剂L-NAME预处理逆转了SNP的这种作用。结论:NO可抑制胃癌细胞生长和增殖,加速细胞凋亡。Objective:To investigate the effect of exogenous nitric oxide(NO) on the growth and proliferation of gastric cancer cell line SGC-7901.Methods:The inhibitory effects of NO donor sodium nitroprusside(SNP) and nitric oxide synthase(NOS) inhibitor N-nitro-L-arginine methylester(L-NAME) on the proliferation of SGC-7901 cells were analyzed by MTT assay.The changes of mRNA and protein expression of proliferating cell nuclear antigen(PCNA) and caspase-3 were examined by RT-PCR and Western blotting.The cell cycle was measured using flow cytometry.Results:Compared with control group,more cells in the SNP group were arrested at G1 and G0 phases(P0.05) and fewer cells were at S phases(P0.05).SNP decreased the speed of cell-cycle progression from G0/G1 phase into S phase.SNP inhibited the proliferation of SGC-7901 cells and reduced the mRNA and protein expressions of PCNA and caspase-3.NOS inhibitor L-NAME reversed the effects of SNP.Conclusion:NO inhibited cell growth and proliferation,but accelerated apoptosis of gastric cancer cells.
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