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DLC-1基因启动子甲基化对于B-ALL的预后价值
引用本文:徐翀,关明,张健,肖艳群,陈慧英,蒋黎敏.DLC-1基因启动子甲基化对于B-ALL的预后价值[J].检验医学,2011,26(7):473-478.
作者姓名:徐翀  关明  张健  肖艳群  陈慧英  蒋黎敏
作者单位:1. 上海市临床检验中心,上海,200126
2. 复旦大学附属华山医院检验医学科和中心实验室,上海,200040
3. 上海交通大学医学院附属上海儿童医学中心检验科,上海,200127
基金项目:上海市自然科学基金资助项目
摘    要:目的观察儿童急性淋巴细胞白血病中肝癌缺失-1(DLC-1)抑癌基因启动子甲基化状态,评估该基因甲基化对于急性B淋巴细胞白血病(B-ALL)的预后价值。方法对40例B-ALL患儿DLC-1启动子甲基化状态与白血病敏感预后指标白血病微小残留病灶(MRD),以及其他对B-ALL预后可能有影响的指标作一比较,评价DLC-1对于B-ALL的预后判断价值,以及是否可以作为B-ALL的独立预后危险因素。结果 DLC-1甲基化阳性的B-ALL患儿的复发率和5年无事件生存率均与DLC-1甲基化阴性患儿差异有统计学意义(P〈0.05)。DLC-1启动子甲基化与MRD的结果分布并不一致(P〉0.05)。但两者同为阳性结果的5例患儿在5年内全都复发,复发率为100%;而两者同为阴性结果的11例患儿,仅1例在5年内复发,复发率为9%。多因素分析显示仅MRD可作为独立的预后危险因素(P=0.017),DLC-1基因甲基化阳性患儿复发风险是甲基化阴性患儿的8.5倍。结论 DLC-1甲基化和MRD都是B-ALL有意义的预后指标,两者结合可为临床提供覆盖面更广的预后信息。DLC-1甲基化也显示了该指标有成为独立预后危险因素的趋势。

关 键 词:DLC-1基因  甲基化  急性B淋巴细胞白血病  预后价值

Prognostic significance of DLC-1 gene promoter methylation in B-ALL
XU Chong,GUAN Ming,ZHANG Jian,XIAO Yanqun,CHEN Huiying,JIANG Limin.Prognostic significance of DLC-1 gene promoter methylation in B-ALL[J].Laboratory Medicine,2011,26(7):473-478.
Authors:XU Chong  GUAN Ming  ZHANG Jian  XIAO Yanqun  CHEN Huiying  JIANG Limin
Institution:1.Shanghai Center for Clinical Laboratory,Shanghai 200126,China;2.Department of Clinical Laboratory,Huashan Hospital,Fudan University,Shanghai 200040,China;3.Department of Clinical Laboratory,Shanghai Children's Medical Center,Shanghai Jiaotong University School of Medicine,Shanghai 200127,China)
Abstract:Objective To observe the status of the deleted in liver cancer-1(DLC-1) gene promoter methylation and estimate the prognostic value in patients with childhood B-cell acute lymphoblastic leukemia(B-ALL).Methods The prognostic significance of DLC-1 methylation status in B-ALL was determined by analyzing the associations among DLC-1 methylation status and the sensitive prognostic factor minimal residual disease(MRD) as well as other potential prognostic factors from 40 patients with childhood B-ALL for evaluating whether it could be an independent risk factor.Results The B-ALL patients with DLC-1 gene methylation had significant different relapse rate and event-free survival rate from those without DLC-1 gene methylation(P0.05).The distribution of the results from DLC-1 methylation status and MRD was significantly different(P0.05).However,all 5 patients with both MRD and DLC-1 gene methylation positive relapsed in 5 years(relapse rate 100%).Only 1 case relapsed in 5 years in 11 patients with the results of both MRD and DLC-1 gene methylation negative(relapse rate: 9%).Multivariable analysis showed that only MRD was a risk factor for the prognosis(P=0.017).The relapse risk of patients with DLC-1 gene methylation was 8.5 times higher than that of patients without DLC-1 gene methylation.Conclusions Both MRD and DLC-1 gene methylation are good markers for the prognosis of B-ALL.The combination of these 2 markers could provide wider coverage of information for prognosis assessment.DLC-1 gene methylation also shows the trends of being an independent risk factor for the prognosis.
Keywords:Deleted in liver cancer-1 gene  Methylation  B-cell acute lymphoblastic leukemia  Prognostic value
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