The University of Texas M.D. Anderson Cancer Center, Houston, TX, 77030, USA.
University of Zurich and University Hospital Zurich, CH-8091, Zurich, Switzerland.
Blood Cancer J. 2022 Jan 11;12(1):5. doi: 10.1038/s41408-021-00603-3.
Treatment with Menin inhibitor (MI) disrupts the interaction between Menin and MLL1 or MLL1-fusion protein (FP), inhibits HOXA9/MEIS1, induces differentiation and loss of survival of AML harboring MLL1 re-arrangement (r) and FP, or expressing mutant (mt)-NPM1. Following MI treatment, although clinical responses are common, the majority of patients with AML with MLL1-r or mt-NPM1 succumb to their disease. Pre-clinical studies presented here demonstrate that genetic knockout or degradation of Menin or treatment with the MI SNDX-50469 reduces MLL1/MLL1-FP targets, associated with MI-induced differentiation and loss of viability. MI treatment also attenuates BCL2 and CDK6 levels. Co-treatment with SNDX-50469 and BCL2 inhibitor (venetoclax), or CDK6 inhibitor (abemaciclib) induces synergistic lethality in cell lines and patient-derived AML cells harboring MLL1-r or mtNPM1. Combined therapy with SNDX-5613 and venetoclax exerts superior in vivo efficacy in a cell line or PD AML cell xenografts harboring MLL1-r or mt-NPM1. Synergy with the MI-based combinations is preserved against MLL1-r AML cells expressing FLT3 mutation, also CRISPR-edited to introduce mtTP53. These findings highlight the promise of clinically testing these MI-based combinations against AML harboring MLL1-r or mtNPM1.
用 Menin 抑制剂(MI)治疗会破坏 Menin 与 MLL1 或 MLL1 融合蛋白(FP)的相互作用,抑制 HOXA9/MEIS1,诱导携带 MLL1 重排(r)和 FP 或表达突变(mt)-NPM1 的 AML 分化和丧失生存能力。尽管 MI 治疗后常出现临床反应,但大多数患有 MLL1-r 或 mt-NPM1 的 AML 患者仍会死于该疾病。本文介绍的临床前研究表明,Menin 的基因敲除或降解或用 MI SNDX-50469 治疗可减少 MLL1/MLL1-FP 靶点,与 MI 诱导的分化和活力丧失有关。MI 治疗还可降低 BCL2 和 CDK6 水平。SNDX-50469 与 BCL2 抑制剂(venetoclax)或 CDK6 抑制剂(abemaciclib)联合治疗可在携带 MLL1-r 或 mtNPM1 的细胞系和患者源性 AML 细胞中诱导协同致死作用。SNDX-5613 和 venetoclax 的联合治疗在携带 MLL1-r 或 mt-NPM1 的细胞系或 PD AML 细胞异种移植中表现出优越的体内疗效。针对表达 FLT3 突变的 MLL1-r AML 细胞,这些基于 MI 的组合仍具有协同作用,这些细胞也经过 CRISPR 编辑引入了 mtTP53。这些发现突出了在临床上测试这些基于 MI 的组合治疗携带 MLL1-r 或 mtNPM1 的 AML 的潜力。