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CEBPA基因的突变状态:使用高分辨率熔解曲线分析进行全面筛查。

CEBPA gene mutational status: a complete screening using high-resolution melt curve analysis.

作者信息

Rázga Filip, Dvoráková Dana, Jurcek Tomás, Jezísková Ivana, Krístková Zlatuse, Mayer Jirí

机构信息

Center of Molecular Biology and Gene Therapy, Department of Internal Medicine-Hemato-Oncology, University Hospital Brno and Masaryk University, Brno, Czech Republic.

出版信息

Mol Diagn Ther. 2009;13(3):195-200. doi: 10.2165/01250444-200913030-00004.

Abstract

In recent years, several independent prognostic factors in cytogenetically normal acute myeloid leukemia (CN-AML) have been reported. Mutations or the expression levels of certain genes have been often used as molecular markers for prediction of a patient's outcome or for evaluation of treatment outcome. One of them, the gene encoding CCAAT/enhanced binding protein alpha (CEBPA), plays an important role in myeloid differentiation and, when mutated, confers a favorable prognosis for patients with CN-AML. Complete mutation screening of the CEBPA gene is therefore beneficial and requires fast, precise, and sensitive diagnostic tools. Thus, for routine diagnostics, we developed a screening method using high-resolution melt curve analysis prior to direct sequencing, where only positive samples (according to reference) are further sequenced. With this approach, all positive and negative patients were successfully distinguished, and the results obtained were in absolute concordance with the direct sequence analysis.

摘要

近年来,已有多项关于细胞遗传学正常的急性髓系白血病(CN-AML)独立预后因素的报道。某些基因的突变或表达水平常被用作预测患者预后或评估治疗效果的分子标志物。其中之一,编码CCAAT/增强子结合蛋白α(CEBPA)的基因,在髓系分化中起重要作用,其发生突变时,可使CN-AML患者预后良好。因此,对CEBPA基因进行全面的突变筛查很有必要,这需要快速、精确且灵敏的诊断工具。所以,为了常规诊断,我们开发了一种在直接测序前使用高分辨率熔解曲线分析的筛查方法,仅对(根据参考标准)阳性样本进行进一步测序。通过这种方法,所有阳性和阴性患者均被成功区分,且所得结果与直接序列分析完全一致。

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