实时荧光定量PCR检测白血病SALL4/BMI-1基因表达的临床应用研究
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摘要
目的:
     通过检测各类型急、慢性白血病SALL4/BMI-1基因的表达,分析各类型白血病的SALL4/BMI-1基因表达情况,为白血病的MRD监测探求一种新的路径,协助临床判断疗效、预测复发、指导治疗。
     方法:
     应用实时荧光定量PCR技术,对处于初诊、完全缓解(complete remission,CR)、复发等不同阶段的60例各类型急、慢性白血病进行SALL4/BMI-1基因的定量检测,并选择10例志愿者(4例正常人、6例非恶性血液病患者)作为对照组。
     结果:
     1.标准品标准曲线的线性关系良好,重复性良好。
     2.SALL4和BMI-1基因在CR的各类型白血病中不表达或低表达,在初诊和复发的各类型白血病中高表达。复发组与初诊组相比,表达量无统计学意义(P>0.05);初诊组及复发组与CR组相比,初诊组及复发组表达量显著高于完全缓解组(P<0.05);初诊组及复发组与对照组相比,表达量有显著差异性(P<0.05),完全缓解组与对照组相比无显著差异性(P>0.05)。其中,SALL4基因在CLL、T-ALL、M3、M4中不表达或低表达;BMI-1基因在T-ALL中不表达或低表达。
     3.BMI-1与SALL4的表达规律一致,两者表达水平有显著相关性(r=0.825,P<0.01)。
     结论:
     应用实时荧光定量PCR技术定量检测SALL4/BMI-1基因,对监测白血病患者MRD状态具有临床适用性,对MRD动态监测有重要的临床价值。
Objective:To investigate the expression of SALL4 and BMI-1 mRNA in different kinds of leukemia patients through testing the expression of SALL4 and BMI-1 mRNA in acute and chronic leukemia patients and seek a mew method of monitoring minimal residual disease (MRD), conduce to judge curative effect pretest relapse、guide treatment.
     Methods:In this experiment, real-time quantitative reverse transcription PCR (RT-PCR) was used for detecting the expression of SALL4 and BM I-1 mRNA in the mononuclear cells of 60 leukemia patients and 10 normal controls.
     Results:The expression of SALL4 n.RNA BMI-1 mRNA in de novo leukemia patients and relapsed patients was higher than that in controls, which significantly decreased at complete remission (CR). The difference between CR group and de novo group and relapsed group was statistically significant (p<0.05). In relapsed patients, the expression of SALL4 mRNA increased, slightly higher than that in de novo leukemia group, but the difference between CR group and de novo group and relapsed group was not statistically significant (p>0.05). The expression pattern of BMI-1 was the same to that of SALL4 except the up-regulation in M3、CLL、M4, and the expression of BMI-1 was positively correlated with that of SALL4 in leukemia (r=0.825,p<0.01).
     Conclusion:Testing the expression of SALL4 and BMI-1 mRNA in acute and chronic leukemia patients make sense for monitoring minimal residual disease..
引文
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