Ferrando Adolfo A, Neuberg Donna S, Staunton Jane, Loh Mignon L, Huard Christine, Raimondi Susana C, Behm Fred G, Pui Ching Hon, Downing James R, Gilliland D Gary, Lander Eric S, Golub Todd R, Look A Thomas
Department of Pediatric Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA 02142, USA.
Cancer Cell. 2002 Feb;1(1):75-87. doi: 10.1016/s1535-6108(02)00018-1.
Human T cell leukemias can arise from oncogenes activated by specific chromosomal translocations involving the T cell receptor genes. Here we show that five different T cell oncogenes (HOX11, TAL1, LYL1, LMO1, and LMO2) are often aberrantly expressed in the absence of chromosomal abnormalities. Using oligonucleotide microarrays, we identified several gene expression signatures that were indicative of leukemic arrest at specific stages of normal thymocyte development: LYL1+ signature (pro-T), HOX11+ (early cortical thymocyte), and TAL1+ (late cortical thymocyte). Hierarchical clustering analysis of gene expression signatures grouped samples according to their shared oncogenic pathways and identified HOX11L2 activation as a novel event in T cell leukemogenesis. These findings have clinical importance, since HOX11 activation is significantly associated with a favorable prognosis, while expression of TAL1, LYL1, or, surprisingly, HOX11L2 confers a much worse response to treatment. Our results illustrate the power of gene expression profiles to elucidate transformation pathways relevant to human leukemia.
人类T细胞白血病可能源于特定染色体易位激活的致癌基因,这些易位涉及T细胞受体基因。我们在此表明,五种不同的T细胞致癌基因(HOX11、TAL1、LYL1、LMO1和LMO2)在无染色体异常的情况下常异常表达。使用寡核苷酸微阵列,我们鉴定了几种基因表达特征,这些特征表明白血病细胞在正常胸腺细胞发育的特定阶段停滞:LYL1+特征(前T细胞)、HOX11+(早期皮质胸腺细胞)和TAL1+(晚期皮质胸腺细胞)。基因表达特征的层次聚类分析根据样本共享的致癌途径对样本进行分组,并确定HOX11L2激活是T细胞白血病发生中的一个新事件。这些发现具有临床重要性,因为HOX11激活与良好预后显著相关,而TAL1、LYL1或令人惊讶的HOX11L2的表达导致对治疗的反应差得多。我们的结果说明了基因表达谱在阐明与人类白血病相关的转化途径方面的作用。