组蛋白去乙酰化酶抑制剂曲古抑菌素A对肝癌细胞蛋白质差异表达谱的影响  被引量:1

Effects fo Trichostatin A on the differentially expressed profile of proteins in hepatocelluar carcinoma

在线阅读下载全文

作  者:范文涛[1] 钟德玝[1] 苗雄鹰[1] 王群伟[1] 黄生福[1] 杨竹林[1] 

机构地区:[1]中南大学湘雅二院肝胆胰外科,长沙410011

出  处:《中华实验外科杂志》2009年第12期1639-1641,共3页Chinese Journal of Experimental Surgery

摘  要:目的观察组蛋白去乙酰化酶(HDAC)抑制剂-曲古抑菌素A(TSA)对肝癌细胞(BEL-7402)蛋白质表达谱的影响。方法采用150g/LTSA处理BEL-7402细胞16hr为试验组,未处理的细胞为对照组,分别抽提其总蛋白质,蛋白定量恒定为200mg。经第一向固相pH梯度等电聚焦电泳和第二向垂直平板SDS—PAGE,凝胶银染后获得二维凝胶图并扫描输入计算机进行软件分析。将三次重复实验所获得的二维凝胶图进行统计学分析。将差异表达的蛋白质斑点从银染后的二维凝胶中切下,进行质谱分析。结果实验组BEL-7402细胞90%~95%的蛋白质表达与对照组一致,5%-10%的蛋白质为差异表达;通过质谱对差异点的鉴定,获得了16个差异表达蛋自质,包括:Triosephosphate isomerase.47-KDa heat shock protein、TRAF1,5(up)、annexin A1、Heat shock 70 protein、prohibitin、thioredoxin peroxidase、DP-1等分子,这些蛋白质涉及基因表达调控、信号转导、细胞代谢、抑制细胞增殖等众多分子事件。结论TSA能够通过影响蛋白质的差异表达影响BEL-7402肝癌细胞的生长和增殖。Objective To study the effects of Trichostatin A (TSA) on the differentially expressed profile of proteins in hepatocelluar carcinoma (HCC). Methods Proteomic technique and microarray were performed to analyze the differentially expressed profile in HCC cell line BEL-7402HCC after treated with 150 mg/ml TSA for 16 h. The 2-D and MS were performed to analyze the effect of TSA on protein expression profile in HCC cells. Results There were 5% -10% differentially expressed proteins. Eight up-regulated proteins and eight down-regulated proteins in the transfected cells were successfully identified by ESI-Q-TOF. These differentially expressed proteins included: riosephosphate isomerase, 47-kD heat shock protein,TRAF1,5 ( up), annexin A1, heat shock 70 protein, prohibitin, thioredoxin peroxidase, DP- 1, and so on. vThese differentially expressed proteins involved cell cycling, transcription regulation, signaling pathway, etc. Conclusion TSA may exert its effect by mediating differential expression of these proteins.

关 键 词: 肝细胞 组蛋白去乙酰化酶 蛋白质组学 

分 类 号:R735.7[医药卫生—肿瘤] R733.7[医药卫生—临床医学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象