Department of Pediatrics, Herman B Wells Center for Pediatric Research.
Department of Medicine.
JCI Insight. 2023 May 8;8(9):e163864. doi: 10.1172/jci.insight.163864.
Loss-of-function mutations in the DNA methyltransferase 3A (DNMT3A) are seen in a large number of patients with acute myeloid leukemia (AML) with normal cytogenetics and are frequently associated with poor prognosis. DNMT3A mutations are an early preleukemic event, which - when combined with other genetic lesions - result in full-blown leukemia. Here, we show that loss of Dnmt3a in hematopoietic stem and progenitor cells (HSC/Ps) results in myeloproliferation, which is associated with hyperactivation of the phosphatidylinositol 3-kinase (PI3K) pathway. PI3Kα/β or the PI3Kα/δ inhibitor treatment partially corrects myeloproliferation, although the partial rescue is more efficient in response to the PI3Kα/β inhibitor treatment. In vivo RNA-Seq analysis on drug-treated Dnmt3a-/- HSC/Ps showed a reduction in the expression of genes associated with chemokines, inflammation, cell attachment, and extracellular matrix compared with controls. Remarkably, drug-treated leukemic mice showed a reversal in the enhanced fetal liver HSC-like gene signature observed in vehicle-treated Dnmt3a-/- LSK cells as well as a reduction in the expression of genes involved in regulating actin cytoskeleton-based functions, including the RHO/RAC GTPases. In a human PDX model bearing DNMT3A mutant AML, PI3Kα/β inhibitor treatment prolonged their survival and rescued the leukemic burden. Our results identify a potentially new target for treating DNMT3A mutation-driven myeloid malignancies.
DNA 甲基转移酶 3A(DNMT3A)的功能丧失性突变可见于大量具有正常细胞遗传学的急性髓系白血病(AML)患者,且常与不良预后相关。DNMT3A 突变是一种早期的白血病前事件,当与其他遗传病变结合时,会导致完全性白血病。在这里,我们表明造血干细胞和祖细胞(HSC/Ps)中 Dnmt3a 的缺失会导致骨髓增生,这与磷酸肌醇 3-激酶(PI3K)途径的过度激活有关。PI3Kα/β 或 PI3Kα/δ 抑制剂治疗部分纠正了骨髓增生,但在对 PI3Kα/β 抑制剂治疗的反应中,部分挽救更为有效。在经药物处理的 Dnmt3a-/-HSC/Ps 的体内 RNA-Seq 分析中,与对照组相比,与趋化因子、炎症、细胞附着和细胞外基质相关的基因表达减少。值得注意的是,与 vehicle-treated Dnmt3a-/-LSK 细胞相比,经药物处理的白血病小鼠表现出增强的胎肝 HSC 样基因特征的逆转,以及参与调节肌动蛋白细胞骨架功能的基因表达减少,包括 RHO/RAC GTPases。在携带 DNMT3A 突变 AML 的人类 PDX 模型中,PI3Kα/β 抑制剂治疗延长了它们的存活时间并减轻了白血病负担。我们的研究结果确定了治疗 DNMT3A 突变驱动的髓样恶性肿瘤的一个潜在新靶点。