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治疗性靶向血液系统恶性肿瘤中的 EP300/CBP 通过溴结构域抑制。

Therapeutic targeting of EP300/CBP by bromodomain inhibition in hematologic malignancies.

机构信息

Leukaemia Biology Laboratory, Cancer Research UK Manchester Institute, The University of Manchester, Manchester M20 4BX, UK.

CellCentric Ltd., Cambridge CB10 1XL, UK.

出版信息

Cancer Cell. 2023 Dec 11;41(12):2136-2153.e13. doi: 10.1016/j.ccell.2023.11.001. Epub 2023 Nov 22.

DOI:10.1016/j.ccell.2023.11.001
PMID:37995682
Abstract

CCS1477 (inobrodib) is a potent, selective EP300/CBP bromodomain inhibitor which induces cell-cycle arrest and differentiation in hematologic malignancy model systems. In myeloid leukemia cells, it promotes rapid eviction of EP300/CBP from an enhancer subset marked by strong MYB occupancy and high H3K27 acetylation, with downregulation of the subordinate oncogenic network and redistribution to sites close to differentiation genes. In myeloma cells, CCS1477 induces eviction of EP300/CBP from FGFR3, the target of the common (4; 14) translocation, with redistribution away from IRF4-occupied sites to TCF3/E2A-occupied sites. In a subset of patients with relapsed or refractory disease, CCS1477 monotherapy induces differentiation responses in AML and objective responses in heavily pre-treated multiple myeloma. In vivo preclinical combination studies reveal synergistic responses to treatment with standard-of-care agents. Thus, CCS1477 exhibits encouraging preclinical and early-phase clinical activity by disrupting recruitment of EP300/CBP to enhancer networks occupied by critical transcription factors.

摘要

CCS1477(inobrodib)是一种有效的、选择性的 EP300/CBP 溴结构域抑制剂,它能诱导血液恶性肿瘤模型系统中的细胞周期停滞和分化。在髓样白血病细胞中,它能迅速将 EP300/CBP 从强 MYB 占据和高 H3K27 乙酰化标记的增强子集中驱逐出去,同时下调下属致癌网络,并重新分配到接近分化基因的位置。在骨髓瘤细胞中,CCS1477 诱导 FGFR3(常见(4;14)易位的靶点)中 EP300/CBP 的驱逐,从 IRF4 占据的位点重新分配到 TCF3/E2A 占据的位点。在一组复发或难治性疾病的患者中,CCS1477 单药治疗可诱导 AML 的分化反应和经大量预处理的多发性骨髓瘤的客观反应。体内临床前联合研究揭示了与标准治疗药物联合治疗的协同反应。因此,CCS1477 通过破坏 EP300/CBP 募集到由关键转录因子占据的增强子网络,显示出令人鼓舞的临床前和早期临床活性。

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