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CC-90009,一种新型的 cereblon E3 连接酶调节剂,靶向急性髓系白血病原始细胞和白血病干细胞。

CC-90009, a novel cereblon E3 ligase modulator, targets acute myeloid leukemia blasts and leukemia stem cells.

机构信息

Bristol-Myers Squibb, San Diego, CA.

Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.

出版信息

Blood. 2021 Feb 4;137(5):661-677. doi: 10.1182/blood.2020008676.

Abstract

A number of clinically validated drugs have been developed by repurposing the CUL4-DDB1-CRBN-RBX1 (CRL4CRBN) E3 ubiquitin ligase complex with molecular glue degraders to eliminate disease-driving proteins. Here, we present the identification of a first-in-class GSPT1-selective cereblon E3 ligase modulator, CC-90009. Biochemical, structural, and molecular characterization demonstrates that CC-90009 coopts the CRL4CRBN to selectively target GSPT1 for ubiquitination and proteasomal degradation. Depletion of GSPT1 by CC-90009 rapidly induces acute myeloid leukemia (AML) apoptosis, reducing leukemia engraftment and leukemia stem cells (LSCs) in large-scale primary patient xenografting of 35 independent AML samples, including those with adverse risk features. Using a genome-wide CRISPR-Cas9 screen for effectors of CC-90009 response, we uncovered the ILF2 and ILF3 heterodimeric complex as a novel regulator of cereblon expression. Knockout of ILF2/ILF3 decreases the production of full-length cereblon protein via modulating CRBN messenger RNA alternative splicing, leading to diminished response to CC-90009. The screen also revealed that the mTOR signaling and the integrated stress response specifically regulate the response to CC-90009 in contrast to other cereblon modulators. Hyperactivation of the mTOR pathway by inactivation of TSC1 and TSC2 protected against the growth inhibitory effect of CC-90009 by reducing CC-90009-induced binding of GSPT1 to cereblon and subsequent GSPT1 degradation. On the other hand, GSPT1 degradation promoted the activation of the GCN1/GCN2/ATF4 pathway and subsequent apoptosis in AML cells. Collectively, CC-90009 activity is mediated by multiple layers of signaling networks and pathways within AML blasts and LSCs, whose elucidation gives insight into further assessment of CC-90009s clinical utility. These trials were registered at www.clinicaltrials.gov as #NCT02848001 and #NCT04336982).

摘要

许多经临床验证的药物都是通过重新利用 CUL4-DDB1-CRBN-RBX1(CRL4CRBN)E3 泛素连接酶复合物与分子胶降解剂来开发的,以消除致病蛋白。在这里,我们介绍了一种首创的 GSPT1 选择性 cereblon E3 连接酶调节剂 CC-90009 的鉴定。生化、结构和分子特征表明,CC-90009 利用 CRL4CRBN 选择性地靶向 GSPT1 进行泛素化和蛋白酶体降解。CC-90009 耗尽 GSPT1 可迅速诱导急性髓系白血病 (AML) 细胞凋亡,减少 35 个独立 AML 样本的大规模原发性患者异种移植中的白血病植入和白血病干细胞 (LSCs),包括具有不良风险特征的样本。使用全基因组 CRISPR-Cas9 筛选 CC-90009 反应的效应器,我们发现 ILF2 和 ILF3 异二聚体复合物是 cereblon 表达的新型调节因子。ILF2/ILF3 缺失会通过调节 CRBN 信使 RNA 可变剪接减少全长 cereblon 蛋白的产生,从而降低对 CC-90009 的反应。该筛选还表明,mTOR 信号和整合应激反应特异性调节对 CC-90009 的反应,与其他 cereblon 调节剂相反。TSC1 和 TSC2 的失活使 mTOR 途径过度激活,通过减少 CC-90009 诱导的 GSPT1 与 cereblon 的结合和随后的 GSPT1 降解,从而保护 AML 细胞免受 CC-90009 的生长抑制作用。另一方面,GSPT1 降解促进了 AML 细胞中 GCN1/GCN2/ATF4 途径的激活和随后的细胞凋亡。总的来说,CC-90009 的活性是由 AML 母细胞和 LSCs 内的多个信号网络和途径介导的,其阐明为进一步评估 CC-90009 的临床实用性提供了线索。这些试验在 www.clinicaltrials.gov 上注册为 #NCT02848001 和 #NCT04336982)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/8215192/b50118322efa/bloodBLD2020008676absf1.jpg

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