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IFN-α联合As2O3对NB4细胞株VEGF及Survivin表达的影响

Effects of interferon-α combining with arsenic trioxide on the expression of VEGF and Survivin in NB4 cell line

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【作者】 王树叶段丽祥曹峰林杨喜晶

【Author】 WANG Shu-ye,DUAN Li-xiang,CAO Feng-lin,et al(Department of Hematology,The First Clinical College,Hospital of Medical University,Harbin 150001,China)

【机构】 哈尔滨医科大学第一临床医学院血液科山西省运城市中心医院

【摘要】 目的探讨IFN-α联合不同浓度As2O3对NB4细胞株血管内皮生长因子(VEGF)、凋亡抑制蛋白(Sur-vivin)表达的影响。方法实验分不同浓度的As2O3即0、0.1、0.5、1.0、2.0μmol/L及不同浓度As2O3联合IFN-α共10组,利用MTT法检测细胞毒性反应,同时采用免疫组织化学方法半定量分析NB4细胞VEGF、Survivin表达的动态变化。结果Survivin在未加药组阳性率为93.8%,VEGF在未加药组阳性率为82.4%。As2O3(≤1.0μmol/L)作用后VEGF表达增加,但无统计学意义;Survivin表达下降(P<0.029)。2.0μmol/L As2O3作用下两者表达均明显降低(P=0.006;P=0.000);联合IFN-α组两者表达均明显降低(P=0.000),分析两者呈正相关(r=0.8754)。结论IFN-α联合As2O3可降低VEGF、Survivin的表达,提示IFN可以降低As2O3对NB4细胞凋亡抑制基因的表达,具有调控细胞凋亡的作用。

【Abstract】 Objective To investigate the expressions of vascular endothelial growth factor(VEGF) and Survivin in NB4 cells lines affected by interferon-α combining with arsenic trioxide.Methods NB4 cells line were treated with arsenic trioxide alone(with doses of 0,0.1,0.5,1.0,2.0μmol/L)or in combination with interferon-α.Cytotoxic reaction was assessed by MTT assay.The dynamic expressions of VEGF and Survivin were detected by semi-quantitative immunohistochemistry.Results The positive rates of VEGF and Survivin in control group were 82.4% and 93.8%,respectively.VEGF expression increased under effect of arsenic trioxide(≤1.0μmol/L)(no statistically significance),instead,Survivin decreased(P<0.029).VEGF and Survivin decreased when treating with 2.0μmol/Larsenic trioxide,as well as combining with interferon-α.Positive correlation was observed between of them(r=0.8754).Conclusion Interferon-α combining with arsenic trioxide can down regulate the expressions of VEGF and Survivin and suggests that interferon-α can decrease the expression of inhibitor of apoptosis gene in NB4 cell line and play a role in the regulation of cell apoptosis.

【基金】 哈尔滨市科学研究基金项目(2005AA9CS116-4);黑龙江省卫生厅医学科研基金(2003-035)
  • 【文献出处】 哈尔滨医科大学学报 ,Journal of Harbin Medical University , 编辑部邮箱 ,2008年06期
  • 【分类号】R733.7
  • 【被引频次】2
  • 【下载频次】45
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