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首页> 外文期刊>Genes, Chromosomes and Cancer >Genome-wide analysis of acute myeloid leukemia with normal karyotype reveals a unique pattern of homeobox gene expression distinct from those with translocation-mediated fusion events.
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Genome-wide analysis of acute myeloid leukemia with normal karyotype reveals a unique pattern of homeobox gene expression distinct from those with translocation-mediated fusion events.

机译:全基因组的急性髓细胞白血病具有正常核型的全基因组分析揭示了同源异型盒基因表达的独特模式,不同于那些易位介导的融合事件。

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摘要

Gene expression profiles were determined from presentation peripheral blood and bone marrow samples of 28 patients with acute myeloid leukemia (AML). Hierarchical clustering sorted the profiles into separate groups, each representing one of the major cytogenetic classes in AML [i.e., t(8;21), t(15;17), inv(16), 11q23, and normal karyotype]. Statistical group comparison identified genes whose expression was strongly correlated with these chromosomal classes. Moreover, the normal karyotype AMLs were characterized by distinctive up-regulation of certain members of the class I homeobox A and B gene families, implying a common underlying genetic lesion. These data reveal novel diagnostic and therapeutic targets and demonstrate the potential of microarray-based dissection of AML.
机译:从表达的28名急性髓细胞性白血病(AML)患者的外周血和骨髓样本中确定基因表达谱。层次聚类将概要文件分为不同的组,每个组代表AML中的主要细胞遗传学类别之一(即t(8; 21),t(15; 17),inv(16),11q23和正常核型)。统计组比较确定了其表达与这些染色体类别密切相关的基因。此外,正常的核型AMLs以I类同源盒A和B基因家族的某些成员的独特上调为特征,这暗示了常见的潜在遗传病灶。这些数据揭示了新的诊断和治疗目标,并证明了基于微阵列的AML解剖的潜力。

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