CEBPA公司
髓样
生物
骨髓生成
造血
髓系白血病
癌症研究
IDH2型
转录因子
运行x1
DNA甲基化
表观遗传学
突变体
祖细胞
突变
IDH1
免疫学
粒细胞生成
细胞生物学
细胞分化
野生型
分子生物学
基因敲除
IRF8
调节器
心理压抑
基因表达调控
祖细胞
作者
Mariam Hakobyan,Jens Langstein,Maria Jose Ramos Medina,Emely Kleinert,Maximilian Schönung,Mark Hartmann,H. Rohdjeß,Jessica Wojtarowicz,Sina Staeble,Melissa Türe,Yasmine Pobiedonoscew,Rainer Claus,Lars Bullinger,Christopher C. Oakes,Katharina Zoldan,Michael Cross,Uwe Platzbecker,Niclas Kneisel,Simon Raffel,U Germing
出处
期刊:Blood
[Elsevier BV]
日期:2026-05-27
卷期号:148 (7): 867-881
被引量:1
标识
DOI:10.1182/blood.2025031268
摘要
ABSTRACT: IDH1 and IDH2 are frequently mutated in various cancers, including acute leukemias. However, the distinct mechanisms by which mutant IDH1 or IDH2 drive hematopoietic neoplasms remain poorly understood. Here, we analyzed DNA methylation in IDH1- and IDH2-mutant acute myeloid leukemia and found neutrophil lineage-specific epigenetic alterations in IDH1-mutant patients that went along with severely impaired neutrophil differentiation. Transcriptional analysis of normal hematopoiesis in humans and mice revealed a strong physiological upregulation of IDH1/Idh1 in myeloid progenitors. To study the functional effects of Idh1 mutations on hematopoiesis in a preleukemic setting, we used a genetically engineered inducible mouse model expressing a heterozygous Idh1 mutation under control of the endogenous promotor. Our study revealed a cell-intrinsic block in neutrophil differentiation caused by repression of myeloid transcription programs in neutrophil progenitors. This included impaired expression of Cebpe, which encodes a key transcription factor regulating neutrophil differentiation. Reactivation of Cebpe expression, by overexpression of its upstream regulator Cebpa or following treatment with hypomethylating agents, restored differentiation, indicating that the differentiation block is reversible. In summary, we found a reversible, preleukemic impairment of neutrophil differentiation in IDH1-mutant hematopoiesis that correlates with elevated IDH1 expression in myeloid progenitors and likely explains the strong association of IDH1 mutations with myeloid neoplasms.
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