ETV6/RUNX1融合基因及其作用

A. Rahnemoon
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引用次数: 0

摘要

最近的研究成功地在一名被诊断为ETV6/RUNXI阳性急性淋巴细胞白血病(ALL)的患者的健康双胞胎中鉴定了白血病前ETV6/RUNX1阳性克隆,并且在小鼠中对ETV6/RUN X1敲除的一些研究表明,融合基因的表达不足以诱导ALL。总之,这些数据表明ETV6/RUNX1阳性白血病是通过多步骤机制产生的,并且额外的基因变化的积累对于显性白血病的发展是必要的。因此,为了充分了解这种疾病的遗传进化,有必要鉴定伴随ETV6/RUNX1融合基因的完整遗传变化谱。此外,通过研究不同拷贝数变化的相关性模式,可以获得关键的病理遗传学见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ETV6/RUNX1 fusion gene and its active role
Recent investigation successfully identified a pre leukemic ETV6/RUNX1-positive clone in the healthy twin of a patient diagnosed with ETV6/RUNXI-positive acute lymphoblastic leukemia (ALL) and also some studies with ETV6/RUNX1 knock in mice showed that the expression of the fusion gene is not sufficient for the invivo induction of ALL. Taken together, these data indicate that ETV6/RUNX1-positive leukemia is .generated through a multi-step mechanism, and that accumulation of additional genetic changes is necessary for the development of overt leukemia. Hence, to understand fully the genetic evolution of this disorder, identification of the complete spectrum of genetic changes that accompany the ETV6/RUNX1 fusion gene is necessary. Moreover, critical patho genetic insights may be gained from studying the correlation pattern of the different copy number changes.
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