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Genomics in Acute Myeloid Leukemia: From Identification to Personalization

机译:急性髓性白血病的基因组学:从鉴定到个性化。

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Acute Myeloid Leukemia (AML) is an aggressive bone marrow malignancy that is fatal if left untreated. Pre- vious classification was strictly based on morphology, which gave little information in terms of prognosis or guide to treatment. Recent research has provided vital information into the chromosomal and molecular patho- genesis of leukemia development. The discovery of these abnormalities via proteomics and genomics have provid- ed two key insights. First, these novel discoveries pro- vide prognostic significance into the predictive result of chemotherapy. Second, these chromosomal and protein abnormalities have provided potential drug targets for new treatment modalities. This article will elaborate on many of these new molecular findings and discuss their implications on the treatment of AML.
机译:急性髓细胞性白血病(AML)是一种侵袭性骨髓恶性肿瘤,如果不加以治疗会致命。先前的分类严格基于形态学,因此从预后或治疗指导方面提供的信息很少。最近的研究为白血病发展的染色体和分子致病机理提供了重要信息。通过蛋白质组学和基因组学发现这些异常现象提供了两个关键的见解。首先,这些新发现为化疗的预测结果提供了预后意义。其次,这些染色体和蛋白质异常为新的治疗方式提供了潜在的药物靶标。本文将详细介绍许多这些新的分子发现,并讨论它们对AML治疗的影响。

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