NFAT家族在急性髓性白血病中的转录调控

IF 0.9 Q4 HEMATOLOGY Hemato Pub Date : 2021-08-27 DOI:10.3390/hemato2030035
S. Patterson, Xu Huang, H. Jørgensen, A. Michie
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引用次数: 2

摘要

急性髓细胞白血病(AML)是一种血液学癌症,由于缺乏有效的靶向治疗,预后较差。活化T细胞核因子(NFAT)转录因子家族是髓系细胞周期和分化的调节因子。最近的证据表明,NFAT家族成员可能在调节AML白血病的发生和对髓系白血病靶向治疗的耐药性方面发挥作用。此外,来自患者样本的基因表达数据显示,一些NFAT在低分化AML和疾病复发后更高表达,这意味着NFAT家族可能在特定类型的AML中发挥作用。这篇综述概述了NFAT在健康髓系组织中作用的证据,并探讨了NFAT如何调节AML发病机制,强调了在AML中靶向特定NFAT蛋白的治疗潜力。
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Transcriptional Regulation by the NFAT Family in Acute Myeloid Leukaemia
Acute myeloid leukaemia (AML) is a haematological cancer with poor outcomes due to a lack of efficacious targeted therapies. The Nuclear Factor of Activated T Cells (NFAT) family of transcription factors is well characterised as a regulator of the cell cycle and differentiation in the myeloid lineage. Recent evidence has demonstrated that NFAT family members may have roles in regulating AML leukemogenesis and resistance to targeted therapy in myeloid leukaemia. Furthermore, gene expression data from patient samples show that some NFATs are more highly expressed in poorly differentiated AML and after disease relapse, implying that the NFAT family may have roles in specific types of AML. This review outlines the evidence for the role of NFAT in healthy myeloid tissue and explores how NFAT might regulate AML pathogenesis, highlighting the potential to target specific NFAT proteins therapeutically in AML.
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CiteScore
1.30
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0.00%
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审稿时长
11 weeks
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