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Gene sets identified with oncogene cooperativity analysis regulate in vivo growth and survival of leukemia stem cells

机译:通过癌基因协同分析鉴定的基因集可调节白血病干细胞的体内生长和存活

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Leukemia stem cells (LSCs) represent a biologically distinct subpopulation of myeloid leukemias, with reduced cell cycle activity and increased resistance to therapeutic challenge. To better characterize key properties of LSCs, we employed a strategy based on identification of genes synergistically dysregulated by cooperating oncogenes. We hypothesized that such genes, termed "cooperation response genes" (CRGs), would represent regulators of LSC growth and survival. Using both a primary mouse model and human leukemia specimens, we show that CRGs comprise genes previously undescribed in leukemia pathogenesis in which multiple pathways modulate the biology of LSCs. In addition, our findings demonstrate that the CRG expression profile can be used as a drug discovery tool for identification of compounds that selectively target the LSC population. We conclude that CRG-based analyses provide a powerful means to characterize the basic biology of LSCs as well as to identify improved methods for therapeutic targeting.
机译:白血病干细胞(LSC)代表了髓样白血病的生物学上独特的亚群,具有降低的细胞周期活性和增加的对治疗挑战的抵抗力。为了更好地表征LSC的关键特性,我们采用了基于鉴定协同合作致癌基因协同失调基因的策略。我们假设这种被称为“合作反应基因”(CRG)的基因将代表LSC生长和存活的调节因子。使用原发性小鼠模型和人类白血病标本,我们显示CRGs包含先前在白血病发病机理中未描述的基因,在该疾病中,多种途径调节LSCs的生物学特性。此外,我们的发现表明CRG表达谱可以用作药物发现工具,用于鉴定选择性靶向LSC群体的化合物。我们得出结论,基于CRG的分析为表征LSC的基本生物学特性以及确定治疗靶向的改进方法提供了有力手段。

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