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作 者:杨丰强[1] 黄建华[1] 郭长城[1] 罗俊[1] 车建平[1] 鄢阳[1] 耿江[1] 邵阳 郑军华[1]
机构地区:[1]同济大学附属第十人民医院泌尿外科,上海200072 [2]武警上海市总队医院泌尿外科,上海201103
出 处:《肿瘤》2013年第3期229-233,共5页Tumor
摘 要:目的:探讨丙戊酸钠(valproate,VPA)对人肾癌ACHN细胞的增殖、细胞周期及凋亡的影响及其可能机制。方法:采用CCK-8法观察VPA对肾癌ACHN细胞的增殖抑制作用。FCM法检测VPA对肾癌ACHN细胞周期和细胞凋亡的影响。实时荧光定量PCR法检测细胞周期调节因子cyclin E1和P^21WAF1以及凋亡调控因子Bcl-2和Bax的m RNA表达。结果:不同浓度的VPA作用于肾癌ACHN细胞48h后均能显著抑制细胞增殖,其半数抑制浓度(50% inhibitory concentration,IC_50)为4.21mmol/L。VPA处理组与对照组相比,G_0/G_1细胞所占比例增加,细胞凋亡率明显增加。4mmol/LVPA处理细胞48h后,cyclin E1 mRNA表达水平明显降低,P^21WAF1mRNA表达量明显增加,Bcl-2mRNA表达水平明显降低,Bax mRNA表达量明显增加。结论:VPA通过诱导细胞周期阻滞和细胞凋亡,抑制肾癌ACHN细胞增殖。Objective: To investigate the effects of VPA (valproate) on proliferation, cell cycle distribution and apoptosis of human kidney carcinoma ACHN cells and the possible underlying mechanisms. Methods:The effect of VPA on the proliferation of ACHN cells was examined by CCK-8 (cell counting kit-8) assay. Flow cytometry was used to analyze the cell cycle distribution and apoptosis of ACHN cells exposed to VPA. The mRNA expressions of cyclin E1, P^21WAF1, Bcl-2 and Bax were detected by real-time fluorescence quantitative-PCR. Results: Incubation with various concentrations of VPA for 48 h resulted in a significant inhibition of proliferation of ACHN cells with an IC50 (50% inhibitory concentration) value of 4.21 mmol/L. After treatment with VPA, the cell cycle was arrested obviously at G0/G1 phase and the apoptotic rate was significantly increased as compared with the control group. After treatment with 4 mmol/L VPA for 48 h, the levels of P^21WAF1 and Bax mRNAs were both significantly increased, and at the same time, the levels of cyclin E1 and Bcl-2 mRNAs were obviously decreased. Conclusion: VPA can inhibit the proliferation of kidney carcinoma ACHN cells by inducing cell-cycle arrest and apoptosis.
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