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STAT3 as a possible therapeutic target in human malignancies: lessons from acute myeloid leukemia

机译:STAT3作为人类恶性肿瘤的可能治疗靶点:急性髓细胞白血病的经验教训

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摘要

STAT3 is important for transcriptional regulation in human acute myeloid leukemia (AML). STAT3 has thousands of potential DNA binding sites but usually shows cell type specific binding preferences to a limited number of these. Furthermore, AML is a very heterogeneous disease, and studies of the prognostic impact of STAT3 in human AML have also given conflicting results. A more detailed characterization of STAT3 functions and the expression of various isoforms in human AML will therefore be required before it is possible to design clinical studies of STAT3 inhibitors in this disease, and it will be especially important to investigate whether the functions of STAT3 differ between patients. Several other malignancies also show extensive biological heterogeneity, and the present discussion and the suggested scientific approaches may thus be relevant for other cancer patients.
机译:STAT3对于人类急性髓细胞白血病(AML)的转录调控非常重要。 STAT3具有成千上万个潜在的DNA结合位点,但通常只显示有限数量的细胞类型特异性结合偏好。此外,AML是一种非常不同的疾病,关于STAT3对人AML的预后影响的研究也得出了相互矛盾的结果。因此,在可能设计针对该疾病的STAT3抑制剂的临床研究之前,将需要对STAT3功能和人类AML中各种同工型的表达进行更详细的表征,并且调查STAT3的功能在不同疾病之间的差异是否特别重要耐心。其他几种恶性肿瘤也表现出广泛的生物学异质性,因此本讨论和所建议的科学方法可能与其他癌症患者相关。

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