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作 者:姚宏伟[1] 孙浩[2] 何鸿保[1] 唐爱国[2]
机构地区:[1]江苏大学临床医学院,江苏镇江212001 [2]江苏大学附属医院泌尿外科,江苏镇江212001
出 处:《江苏大学学报(医学版)》2011年第1期46-49,共4页Journal of Jiangsu University:Medicine Edition
摘 要:目的:观察组蛋白去乙酰化酶抑制剂曲古霉素A(trichostatin A,TSA)体外对人肾细胞癌Caki-1细胞生长情况、乙酰化组蛋白H3的水平以及基因P21cip1/waf1mRNA表达的影响,并探讨其可能的作用机制。方法:四甲基偶氮唑盐(MTT)比色法检测TSA对Caki-1细胞生长的影响;蛋白质印迹法检测TSA处理后Caki-1细胞乙酰化组蛋白H3水平的变化;实时荧光定量PCR检测TSA处理后Caki-1细胞P21cip1/waf1mRNA表达水平的变化。结果:TSA对Caki-1细胞生长有显著的抑制作用,呈明显的剂量、时间依赖性。TSA能明显提高Caki-1细胞乙酰化组蛋白H3的水平,促进P21cip1/waf1mRNA表达。结论:TSA对人肾细胞癌Caki-1细胞生长有抑制作用,机制可能与其提高Caki-1细胞乙酰化组蛋白H3的水平,促进P21cip1/waf1的表达有关。Objective: To investigate the effect of trichostatin A(TSA),a histone deacetylace inhibitor,on the growth of human renal cell carcinoma Caki-1 cells in vitro,the levels of acetylated histone H3 and the mRNA expression of P21cip1/waf1 gene,then to explore the mechanism involved.Methods: MTT assay was used to examine the effect of TSA on the growth of Caki-1 cells.The levels of acetylated histone H3 after TSA treatment was evaluated by western blot.The mRNA expression of P21cip1/waf1 was analyzed by qRT-PCR.Results: TSA obviously inhibited the growth of Caki-1 cells in a time and dose dependent manner.TSA obviously enhanced the levels of acetylated histone H3 and induced the expression of P21cip1/waf1 mRNA.Conclusion: TSA can induce the growth arrest of human renal cell carcinoma Caki-1 cells,which might be related to increase the levels of acetylated histone H3 and induce the expression of P21cip1/waf1.
关 键 词:曲古霉素A 肾细胞癌 组蛋白 乙酰化 P21CIP1/WAF1
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