Enhancer recruitment of a RUNX1, HDAC1 and TLE3 co-repressor complex by mis-expressed FOXC1 blocks differentiation in acute myeloid leukemia.

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2021-11-19 eCollection Date: 2021-01-01 DOI:10.1080/23723556.2021.2003161
Fabrizio Simeoni, Tim Cp Somervaille
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引用次数: 0

Abstract

Tissue-inappropriate expression of FOXC1 (Forkhead Box C1) in acute myeloid leukemia confers a monocyte/macrophage lineage differentiation block. We discovered that FOXC1 interacts with RUNX1 (Runt-Related Transcription Factor 1) to stabilize a RUNX1, HDAC1 (Histone Deacetylase 1) and TLE3 (Transducin-like enhancer protein 3) repressor complex at enhancers controlling myeloid differentiation genes.

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错误表达的FOXC1对RUNX1、HDAC1和TLE3共阻遏物复合物的增强子募集阻断急性髓系白血病的分化
摘要FOXC1(叉头盒C1)在急性髓系白血病中的组织不恰当表达导致单核细胞/巨噬细胞谱系分化阻滞。我们发现FOXC1与RUNX1(Runt相关转录因子1)相互作用,在控制骨髓分化基因的增强子处稳定RUNX1、HDAC1(组蛋白脱乙酰酶1)和TLE3(转导样增强子蛋白3)阻遏物复合物。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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