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首页> 外文期刊>Genes, Chromosomes and Cancer >T-cell lymphoblastic lymphoma shows differences and similarities with T-cell acute lymphoblastic leukemia by genomic and gene expression analyses.
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T-cell lymphoblastic lymphoma shows differences and similarities with T-cell acute lymphoblastic leukemia by genomic and gene expression analyses.

机译:T细胞淋巴母细胞性淋巴瘤通过基因组和基因表达分析显示出与T细胞急性淋巴细胞性白血病的异同。

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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.
机译: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,并用相似的治疗方法进行治疗。但是,它们显示出不同的临床表现,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谱分析方法。在20个T-LBL和10个T-ALL诊断标本上进行的全基因组基因表达谱分析显示,这两个恶性肿瘤共享其转录谱的很大一部分,而一部分基因似乎在T-LBL与T中差异表达-所有。该特征包括涉及趋化反应和血管生成的基因,其可能在肿瘤细胞定位中起作用。对通过基因表达谱分析的一部分样品进行了全基因组拷贝数变化分析,并检测到41个反复变化的遗传基因座。尽管在两个实体中都发现了大多数像差,但在T-LBL或T-ALL中有选择地识别了一些像差。此外,发现NOTCH1突变状态与遗传畸变的一个子集相关。综上所述,这些结果表明T-LBL和T-ALL确实是两种具有独特的转录和遗传特征的截然不同的疾病。

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