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针对 MLL 重排或 NPM1 突变(NPM1c)的 AML 采用有效的 Menin 抑制剂联合治疗。

Effective Menin inhibitor-based combinations against AML with MLL rearrangement or NPM1 mutation (NPM1c).

机构信息

The University of Texas M.D. Anderson Cancer Center, Houston, TX, 77030, USA.

University of Zurich and University Hospital Zurich, CH-8091, Zurich, Switzerland.

出版信息

Blood Cancer J. 2022 Jan 11;12(1):5. doi: 10.1038/s41408-021-00603-3.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eb1/8752621/05ce86704829/41408_2021_603_Fig1_HTML.jpg

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