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Engineering mouse models with myelodysplastic syndrome human candidate genes; how relevant are they?

机译:具有骨髓增生异常综合症人类候选基因的工程小鼠模型;它们的相关性如何?

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摘要

Myelodysplastic syndromes represent particularly challenging hematologic malignancies that arise from a large spectrum of genetic events resulting in a disease characterized by a range of different presentations and outcomes. Despite efforts to classify and identify the key genetic events, little improvement has been made in therapies that will increase patient survival. Animal models represent powerful tools to model and study human diseases and are useful pre-clinical platforms. In addition to enforced expression of candidate oncogenes, gene inactivation has allowed the consequences of the genetic effects of human myelodysplastic syndrome to be studied in mice. This review aims to examine the animal models expressing myelodysplastic syndrome-associated genes that are currently available and to highlight the most appropriate model to phenocopy myelodysplastic syndrome disease and its risk of transformation to acute myelogenous leukemia.
机译:骨髓增生异常综合症代表着特别具有挑战性的血液系统恶性肿瘤,这种恶性肿瘤是由多种遗传事件引起的,导致一系列疾病的临床表现和结果不同。尽管努力对关键的遗传事件进行分类和鉴定,但是在增加患者存活率的疗法方面几乎没有改善。动物模型代表了用于建模和研究人类疾病的强大工具,并且是有用的临床前平台。除了候选癌基因的强制表达外,基因失活还允许在小鼠中研究人类骨髓增生异常综合症的遗传效应的后果。这篇综述的目的是检查目前可获得的表达与骨髓增生异常综合征相关基因的动物模型,并突出显示最适合表型骨髓增生异常综合征疾病及其转化为急性骨髓性白血病的风险的模型。

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