Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
Division of Experimental Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Nat Commun. 2024 Oct 9;15(1):8747. doi: 10.1038/s41467-024-53158-9.
CBFA2T3-GLIS2 is a fusion oncogene found in pediatric acute megakaryoblastic leukemia that is associated with a poor prognosis. We establish a model of CBFA2T3-GLIS2 driven acute megakaryoblastic leukemia that allows the distinction of fusion specific changes from those that reflect the megakaryoblast lineage of this leukemia. Using this model, we map fusion genome wide binding that in turn imparts the characteristic transcriptional signature. A network of transcription factor genes bound and upregulated by the fusion are found to have downstream effects that result in dysregulated signaling of developmental pathways including NOTCH, Hedgehog, TGFβ, and WNT. Transcriptional regulation is mediated by homo-dimerization and binding of the ETO transcription factor through the nervy homology region 2. Loss of nerve homology region 2 abrogated the development of leukemia, leading to downregulation of JAK/STAT, Hedgehog, and NOTCH transcriptional signatures. These data contribute to the understanding of CBFA2T3-GLIS2 mediated leukemogenesis and identify potential therapeutic vulnerabilities for future studies.
CBFA2T3-GLIS2 是一种融合癌基因,存在于小儿急性巨核细胞白血病中,与预后不良相关。我们建立了一个由 CBFA2T3-GLIS2 驱动的急性巨核细胞白血病模型,该模型允许区分融合特异性变化和反映这种白血病巨核细胞系的变化。使用该模型,我们绘制了融合的全基因组结合图谱,进而赋予了特征性的转录特征。发现融合结合并上调的转录因子基因具有下游效应,导致发育途径(包括 NOTCH、Hedgehog、TGFβ 和 WNT)的信号失调。转录调控是通过 ETO 转录因子通过 nervy 同源区 2 的同源二聚化和结合来介导的。神经同源区 2 的缺失消除了白血病的发展,导致 JAK/STAT、Hedgehog 和 NOTCH 转录特征的下调。这些数据有助于理解 CBFA2T3-GLIS2 介导的白血病发生,并为未来的研究确定潜在的治疗弱点。