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T 细胞淋巴母细胞淋巴瘤通过基因组和基因表达分析显示出与 T 细胞急性淋巴细胞白血病的差异和相似之处。

T-cell lymphoblastic lymphoma shows differences and similarities with T-cell acute lymphoblastic leukemia by genomic and gene expression analyses.

机构信息

Institute for Cancer Genetics, Columbia University, New York, NY10032, USA.

出版信息

Genes Chromosomes Cancer. 2011 Dec;50(12):1063-75. doi: 10.1002/gcc.20924. Epub 2011 Aug 30.

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) and lymphoma (T-LBL) share common morphological and immunophenotypic features and are treated with similar therapeutic approaches. Nonetheless, they show distinct clinical presentations, suggesting that they may represent two different biological entities. To investigate the genetic characteristics of T-LBL and T-ALL, we used genomic and transcriptional profiling approaches. Genome-wide gene expression profiling, performed on 20 T-LBL and 10 T-ALL diagnostic specimens, revealed that the two malignancies shared a large fraction of their transcriptional profile while a subset of genes appeared to be differentially expressed in T-LBL versus T-ALL. This signature included genes involved in chemotactic responses and angiogenesis, which may play a role in tumor cell localization. Genome-wide copy number alteration analysis was performed on a subset of the samples analyzed by gene expression profiling and detected 41 recurrently altered genetic loci. Although most aberrations were found in both entities, several were selectively identified in T-LBL or T-ALL. In addition, NOTCH1 mutational status was found to correlate with a subset of genetic aberrations. Taken together, these results suggest that T-LBL and T-ALL are indeed two distinct diseases with unique transcriptional and genetic characteristics.

摘要

T 细胞急性淋巴细胞白血病 (T-ALL) 和淋巴瘤 (T-LBL) 具有共同的形态学和免疫表型特征,并且采用相似的治疗方法进行治疗。尽管如此,它们表现出不同的临床表现,这表明它们可能代表两种不同的生物学实体。为了研究 T-LBL 和 T-ALL 的遗传特征,我们使用了基因组和转录组谱分析方法。对 20 例 T-LBL 和 10 例 T-ALL 诊断标本进行全基因组基因表达谱分析,结果表明这两种恶性肿瘤具有很大一部分共同的转录谱,而一小部分基因在 T-LBL 与 T-ALL 之间似乎存在差异表达。该特征包括参与趋化反应和血管生成的基因,这些基因可能在肿瘤细胞定位中发挥作用。对通过基因表达谱分析进行分析的样本子集进行了全基因组拷贝数改变分析,检测到 41 个经常发生改变的遗传位点。尽管大多数异常存在于两种实体中,但在 T-LBL 或 T-ALL 中选择性地发现了几个异常。此外,NOTCH1 突变状态与一组遗传异常相关。总之,这些结果表明 T-LBL 和 T-ALL 确实是两种具有独特转录和遗传特征的不同疾病。

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