Li Zejuan, Luo Roger T, Mi Shuangli, Sun Miao, Chen Ping, Bao Jingyue, Neilly Mary Beth, Jayathilaka Nimanthi, Johnson Deborah S, Wang Lili, Lavau Catherine, Zhang Yanming, Tseng Charles, Zhang Xiuqing, Wang Jian, Yu Jun, Yang Huanming, Wang San Ming, Rowley Janet D, Chen Jianjun, Thirman Michael J
Department of Medicine, University of Chicago, Chicago, Illinois, USA.
Cancer Res. 2009 Feb 1;69(3):1109-16. doi: 10.1158/0008-5472.CAN-08-3381. Epub 2009 Jan 20.
Important biological and pathologic properties are often conserved across species. Although several mouse leukemia models have been well established, the genes deregulated in both human and murine leukemia cells have not been studied systematically. We performed a serial analysis of gene expression in both human and murine MLL-ELL or MLL-ENL leukemia cells and identified 88 genes that seemed to be significantly deregulated in both types of leukemia cells, including 57 genes not reported previously as being deregulated in MLL-associated leukemias. These changes were validated by quantitative PCR. The most up-regulated genes include several HOX genes (e.g., HOX A5, HOXA9, and HOXA10) and MEIS1, which are the typical hallmark of MLL rearrangement leukemia. The most down-regulated genes include LTF, LCN2, MMP9, S100A8, S100A9, PADI4, TGFBI, and CYBB. Notably, the up-regulated genes are enriched in gene ontology terms, such as gene expression and transcription, whereas the down-regulated genes are enriched in signal transduction and apoptosis. We showed that the CpG islands of the down-regulated genes are hypermethylated. We also showed that seven individual microRNAs (miRNA) from the mir-17-92 cluster, which are overexpressed in human MLL rearrangement leukemias, are also consistently overexpressed in mouse MLL rearrangement leukemia cells. Nineteen possible targets of these miRNAs were identified, and two of them (i.e., APP and RASSF2) were confirmed further by luciferase reporter and mutagenesis assays. The identification and validation of consistent changes of gene expression in human and murine MLL rearrangement leukemias provide important insights into the genetic base for MLL-associated leukemogenesis.
重要的生物学和病理学特性通常在物种间保守。尽管已经建立了几种小鼠白血病模型,但尚未系统研究在人类和小鼠白血病细胞中失调的基因。我们对人类和小鼠的MLL-ELL或MLL-ENL白血病细胞进行了基因表达的序列分析,鉴定出88个似乎在两种类型的白血病细胞中均显著失调的基因,其中包括57个先前未报道在MLL相关白血病中失调的基因。这些变化通过定量PCR得到验证。上调最明显的基因包括几个HOX基因(如HOX A5、HOXA9和HOXA10)和MEIS1,它们是MLL重排白血病的典型标志。下调最明显的基因包括LTF、LCN2、MMP9、S100A8、S100A9、PADI4、TGFBI和CYBB。值得注意的是,上调的基因在基因本体术语中富集,如基因表达和转录,而下调的基因在信号转导和凋亡中富集。我们发现下调基因的CpG岛发生了高甲基化。我们还发现,在人类MLL重排白血病中过表达的来自mir-17-92簇的7个个体微小RNA(miRNA)在小鼠MLL重排白血病细胞中也持续过表达。鉴定出了这些miRNA的19个可能靶点,其中两个(即APP和RASSF2)通过荧光素酶报告基因和诱变试验得到进一步证实。人类和小鼠MLL重排白血病中基因表达一致变化的鉴定和验证为MLL相关白血病发生的遗传基础提供了重要见解。