Gamma Jay M, Liu Qiang, Beauchamp Erwan, Iyer Aishwarya, Yap Megan C, Zak Zoulika, Ekstrom Cassidy, Pain Rony, Kostiuk Morris A, Mackey John R, Brandwein Joseph, Wang Jean C Y, Berthiaume Luc G
Department of Medicine, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Canada.
Department of Cell Biology, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Canada.
Mol Cancer Ther. 2025 Jan 2;24(1):69-80. doi: 10.1158/1535-7163.MCT-24-0307.
Acute myeloid leukemia (AML) is a hematologic malignancy with limited treatment options and a high likelihood of recurrence after chemotherapy. We studied N-myristoylation, the myristate modification of proteins linked to survival signaling and metabolism, as a potential therapeutic target for AML. N-myristoylation is catalyzed by two N-myristoyltransferases (NMT), NMT1 and NMT2, with varying expressions in AML cell lines and patient samples. We identified NMT2 expression as a marker for survival of patients with AML, and low NMT2 expression was associated with poor outcomes. We used the first-in-class pan-NMT inhibitor, zelenirstat, to investigate the role of N-myristoylation in AML. Zelenirstat effectively inhibits myristoylation in AML cell lines and patient samples, leading to degradation of Src family kinases, induction of endoplasmic reticulum stress, apoptosis, and cell death. Zelenirstat was well tolerated in vivo and reduced the leukemic burden in an ectopic AML cell line and in multiple orthotopic AML patient-derived xenograft models. The leukemia stem cell-enriched fractions of the hierarchical OCI-AML22 model were highly sensitive to myristoylation inhibition. Zelenirstat also impairs mitochondrial complex I and oxidative phosphorylation, which are critical for leukemia stem cell survival. These findings suggest that targeting N-myristoylation with zelenirstat represents a novel therapeutic approach for AML, with promise in patients with currently poor outcomes.
急性髓系白血病(AML)是一种血液系统恶性肿瘤,治疗选择有限,化疗后复发可能性高。我们研究了N-肉豆蔻酰化,即与生存信号传导和代谢相关的蛋白质的肉豆蔻酸修饰,作为AML的潜在治疗靶点。N-肉豆蔻酰化由两种N-肉豆蔻酰转移酶(NMT)NMT1和NMT2催化,在AML细胞系和患者样本中表达各异。我们将NMT2表达确定为AML患者生存的标志物,低NMT2表达与不良预后相关。我们使用了一流的泛NMT抑制剂泽勒尼司他,来研究N-肉豆蔻酰化在AML中的作用。泽勒尼司他可有效抑制AML细胞系和患者样本中的肉豆蔻酰化,导致Src家族激酶降解、内质网应激诱导、细胞凋亡和细胞死亡。泽勒尼司他在体内耐受性良好,可降低异位AML细胞系和多种原位AML患者来源的异种移植模型中的白血病负担。分层OCI-AML22模型中富含白血病干细胞的部分对肉豆蔻酰化抑制高度敏感。泽勒尼司他还损害线粒体复合体I和氧化磷酸化,而这对白血病干细胞存活至关重要。这些发现表明,用泽勒尼司他靶向N-肉豆蔻酰化代表了一种针对AML的新型治疗方法,对目前预后较差的患者有前景。