Song Ju Han, Kim Hyeoung-Joon, Lee Chang Hyun, Kim Seung Jun, Hwang Seung Yong, Kim Tae Sung
College of Pharmacy, Chonnam National University, Gwangju, Republic of Korea.
Int J Oncol. 2006 Jul;29(1):57-64.
Although the methods by which leukemia is classified have been improved for effective therapies, leukemia patients occasionally exhibit diverse, sometimes unpredictable, responses to treatment. Consequently, these patients also evidence individually different clinical courses when administered with anti-leukemia drugs. In order to find new, more precise molecular markers for leukemia classification, we have analyzed the gene expression profiles from 65 diagnostic bone marrow specimens of adult patients with AML, ALL, CML or CLL by using high-throughput DNA microarrays harboring approximately 8,300 unique human genes or expression sequence tags. In the present study, we identified a group of leukemia-specific genes, which manifest gene expression profiles distinctly representative of normal bone marrow samples, as determined by a significance analysis of microarray (SAM) and GeneSpring 6.1 programs. We also determined the minimal number of genes showing a difference between acute and chronic leukemia patient groups. Furthermore, the unsupervised cluster analysis revealed a gene subset which can be used to distinguish between AML, ALL, CML and CLL patient groups, based on expression signatures. The expression levels of differentially regulated genes were verified via the principle component analysis (PCA). Our results may provide a novel set of molecular criteria for the classification of leukemia patients, and may also facilitate effects to discovery new targets, allowing for more effective treatment of leukemia patients.
尽管白血病的分类方法已得到改进以实现有效治疗,但白血病患者对治疗的反应偶尔会表现出多样,有时甚至不可预测。因此,这些患者在使用抗白血病药物时也会呈现出个体不同的临床病程。为了找到用于白血病分类的新的、更精确的分子标志物,我们使用包含约8300个独特人类基因或表达序列标签的高通量DNA微阵列,分析了65例成年急性髓系白血病(AML)、急性淋巴细胞白血病(ALL)、慢性髓系白血病(CML)或慢性淋巴细胞白血病(CLL)患者诊断性骨髓标本的基因表达谱。在本研究中,我们通过微阵列显著性分析(SAM)和GeneSpring 6.1程序确定,鉴定出一组白血病特异性基因,其表现出与正常骨髓样本明显不同的基因表达谱。我们还确定了急性和慢性白血病患者组之间显示差异的最小基因数量。此外,无监督聚类分析揭示了一个基因子集,可根据表达特征用于区分AML、ALL、CML和CLL患者组。通过主成分分析(PCA)验证了差异调节基因的表达水平。我们的结果可能为白血病患者的分类提供一组新的分子标准,也可能有助于发现新靶点,从而更有效地治疗白血病患者。