Department of Haematology, University of Cambridge, Cambridge Institute for Medical Research, Hills Road, Cambridge, CB2 0XY, UK.
Stem Cell Res Ther. 2011 Apr 27;2(2):21. doi: 10.1186/scrt62.
In a recent interesting article, analysis of gene expression between phenotypically defined acute myeloid leukemia (AML) leukemia stem cells (LSCs) and more mature leukemia progenitor cells is used to generate a differentially expressed gene signature for LSCs. Through clever bioinformatic weighting analysis, the authors describe a method to convert this signature into a single score for any given sample and then test the prognostic utility of this 'LSC score' in publicly available gene expression profiles from bulk AML samples. They demonstrate that a high LSC score is associated with poor prognosis in AML patients and further demonstrate that the score is independent of known prognostic factors, including age, karyotype and mutation of the FLT3 or NPM1 genes. These findings are important and directly relate transcriptional dysregulation in AML LSCs with the outcome in patient samples, thus reinforcing the belief that these cellular populations are crucial for the initial propagation and subsequent relapse and resistance of leukemia.
在最近的一篇有趣的文章中,对表型定义的急性髓系白血病 (AML) 白血病干细胞 (LSCs) 和更成熟的白血病祖细胞之间的基因表达进行分析,从而为 LSCs 生成差异表达基因特征。通过巧妙的生物信息加权分析,作者描述了一种将该特征转换为任何给定样本的单个评分的方法,然后测试该“LSC 评分”在来自大量 AML 样本的公开基因表达谱中的预后效用。他们表明,高 LSC 评分与 AML 患者的预后不良相关,并进一步表明该评分独立于已知的预后因素,包括年龄、核型以及 FLT3 或 NPM1 基因突变。这些发现很重要,直接将 AML LSCs 中的转录失调与患者样本的结果联系起来,从而进一步证实这些细胞群体对于白血病的初始传播以及随后的复发和耐药性至关重要。