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The RUNX1 Transcription Factor: A Gatekeeper in Acute Leukemia

机译:Runx1转录因子:急性白血病中的守门人

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The RUNX1 gene, which encodes a transcription factor, is a common target of genetic mutations in acute leukemia. We propose that RUNX1 is a gatekeeper gene, the disruption of which leads to the exodus of a subset of selfrenewing “stem” cells from the normal environmental controls of homeostasis. This pool of “escaped” cells is the target of secondary mutations, accumulating over time to induce the aggressive manifestation of acute leukemia. Evidence from patient and animal studies support the concept that RUNX1 mutations are the initiating event in different leukemia subtypes, but also suggests that diverse mechanisms are used to subvert RUNX1 function. One common result is the inhibition of differentiation – but its effect impinges on different lineages and stages of differentiation, depending on the mutation. A number of different approaches have led to the identification of a few secondary events that lead to the overt acute phase, however, the majority are unknown. Finally, the concept of the “leukemic stem cell” and its therapeutic importance is discussed in light of the RUNX1 gatekeeper function.
机译:编码转录因子的Runx1基因是急性白血病中遗传突变的常见目标。我们提出Runx1是一种术语基因,其破坏导致来自稳态的正常环境控制的自漂白“茎”细胞的exodus。这种“被逃脱”细胞的池是二次突变的靶标,随着时间的推移累积,诱导急性白血病的激进表现。来自患者和动物研究的证据支持Runx1突变是不同白血病亚型的启动事件的概念,但也表明多样化的机制用于颠覆runx1函数。一种常见的结果是抑制分化 - 但其效果根据突变施加不同谱系和分化的阶段。许多不同的方法导致了一些导致公开急性阶段的一些二级事件的识别,然而,大多数是未知的。最后,根据Runx1 Gatekeeper功能讨论了“白血病干细胞”的概念及其治疗重要性。

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