Transcriptional Regulation by the NFAT Family in Acute Myeloid Leukaemia

被引:3
作者
Patterson, Shaun D. [1 ]
Huang, Xu [1 ]
Jorgensen, Heather G. [1 ]
Michie, Alison M. [1 ]
机构
[1] Univ Glasgow, Inst Canc Sci, Coll MVLS, Paul OGorman Leukaemia Res Ctr, Glasgow G120ZD, Scotland
来源
HEMATO | 2021年 / 2卷 / 03期
关键词
leukaemia; NFAT; myeloid; cell cycle; differentiation; AML; ACTIVATED-T-CELLS; NUCLEAR-FACTOR; GENE-EXPRESSION; CD34(+) CELLS; C/EBP-ALPHA; KAPPA-B; IDENTIFICATION; CALCINEURIN; PROTEINS; FLT3;
D O I
10.3390/hemato2030035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:556 / 571
页数:16
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