Yan Han, Wen Lu, Tan Dan, Xie Pan, Pang Feng-Mei, Zhou Hong-Hao, Zhang Wei, Liu Zhao-Qian, Tang Jie, Li Xi, Chen Xiao-Ping
Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha 410078, P. R. China.
Oncotarget. 2017 Jan 3;8(1):1529-1540. doi: 10.18632/oncotarget.13650.
The prognosis of cytogenetically normal acute myeloid leukemia (CN-AML) varies greatly among patients. Achievement of complete remission (CR) after chemotherapy is indispensable for a better prognosis. To develop a gene signature predicting overall survival (OS) in CN-AML, we performed data mining procedure based on whole genome expression data of both blood cancer cell lines and AML patients from open access database. A gene expression signature including 42 probes was derived. These probes were significantly associated with both cytarabine half maximal inhibitory concentration values in blood cancer cell lines and OS in CN-AML patients. By using cox regression analysis and linear regression analysis, a chemo-sensitive score calculated algorithm based on mRNA expression levels of the 42 probes was established. The scores were associated with OS in both the training sample (p=5.13 × 10-4, HR=2.040, 95% CI: 1.364-3.051) and the validation sample (p=0.002, HR=2.528, 95% CI: 1.393-4.591) of the GSE12417 dataset from Gene Expression Omnibus. In The Cancer Genome Atlas (TCGA) CN-AML patients, higher scores were found to be associated with both worse OS (p=0.013, HR=2.442, 95% CI: 1.205-4.950) and DFS (p=0.015, HR=2.376, 95% CI: 1.181-4.779). Results of gene ontology (GO) analysis showed that all the significant GO Terms were correlated with cellular component of mitochondrion. In summary, a novel gene set that could predict prognosis of CN-AML was identified presently, which provided a new way to identify genes impacting AML chemo-sensitivity and prognosis.
细胞遗传学正常的急性髓系白血病(CN-AML)患者的预后差异很大。化疗后实现完全缓解(CR)对于改善预后至关重要。为了开发一种预测CN-AML总生存期(OS)的基因特征,我们基于开放获取数据库中血癌细胞系和AML患者的全基因组表达数据进行了数据挖掘程序。得出了一个包含42个探针的基因表达特征。这些探针与血癌细胞系中的阿糖胞苷半数最大抑制浓度值以及CN-AML患者的OS均显著相关。通过使用cox回归分析和线性回归分析,建立了一种基于这42个探针的mRNA表达水平计算化疗敏感性评分的算法。这些评分在来自基因表达综合数据库的GSE12417数据集的训练样本(p = 5.13×10 -4,HR = 2.040,95%CI:1.364 - 3.051)和验证样本(p = 0.002,HR = 2.528,95%CI:1.393 - 4.591)中均与OS相关。在癌症基因组图谱(TCGA)的CN-AML患者中,发现较高的评分与较差的OS(p = 0.013,HR = 2.442,95%CI:1.205 - 4.950)和无病生存期(DFS)(p = 0.015,HR = 2.376,95%CI:1.181 - 4.779)均相关。基因本体(GO)分析结果表明,所有显著的GO术语均与线粒体的细胞成分相关。总之,目前鉴定出了一种可预测CN-AML预后的新基因集,这为鉴定影响AML化疗敏感性和预后的基因提供了一种新方法。