Developmental Therapeutics Branch and Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
Mol Cancer Ther. 2024 Jul 2;23(7):911-923. doi: 10.1158/1535-7163.MCT-23-0402.
Ataxia telangiectasia and Rad3-related (ATR) checkpoint kinase inhibitors are in clinical trials. Here we explored the molecular pharmacology and therapeutic combination strategies of the oral ATR inhibitor M1774 (Tuvusertib) with DNA-damaging agents (DDA). As single agent, M1774 suppressed cancer cell viability at nanomolar concentrations, showing greater activity than ceralasertib and berzosertib, but less potency than gartisertib and elimusertib in the small cell lung cancer H146, H82, and DMS114 cell lines. M1774 also efficiently blocked the activation of the ATR-CHK1 checkpoint pathway caused by replication stress induced by TOP1 inhibitors. Combination with non-toxic dose of M1774 enhanced TOP1 inhibitor-induced cancer cell death by enabling unscheduled replication upon replicative damage, thereby increasing genome instability. Tandem mass tag-based quantitative proteomics uncovered that M1774, in the presence of DDA, forces the expression of proteins activating replication (CDC45) and G2-M progression (PLK1 and CCNB1). In particular, the fork protection complex proteins (TIMELESS and TIPIN) were enriched. Low dose of M1774 was found highly synergistic with a broad spectrum of clinical DDAs including TOP1 inhibitors (SN-38/irinotecan, topotecan, exatecan, and exatecan), the TOP2 inhibitor etoposide, cisplatin, the RNA polymerase II inhibitor lurbinectedin, and the PARP inhibitor talazoparib in various models including cancer cell lines, patient-derived organoids, and mouse xenograft models. Furthermore, we demonstrate that M1774 reverses chemoresistance to anticancer DDAs in cancer cells lacking SLFN11 expression, suggesting that SLFN11 can be utilized for patient selection in upcoming clinical trials.
共济失调毛细血管扩张症和 Rad3 相关(ATR)检查点激酶抑制剂正在临床试验中。在这里,我们探索了口服 ATR 抑制剂 M1774(Tuvusertib)与 DNA 损伤剂(DDA)的分子药理学和联合治疗策略。作为单一药物,M1774 以纳摩尔浓度抑制癌细胞活力,在小细胞肺癌 H146、H82 和 DMS114 细胞系中比 ceralasertib 和 berzosertib 更有效,但比 gartisertib 和 elimusertib 活性低。M1774 还能有效阻断拓扑异构酶 1 抑制剂诱导的复制应激引起的 ATR-CHK1 检查点通路的激活。与非毒性剂量的 M1774 联合使用可通过在复制损伤时进行无计划复制来增强拓扑异构酶 1 抑制剂诱导的癌细胞死亡,从而增加基因组不稳定性。串联质量标签定量蛋白质组学发现,在 DDA 的存在下,M1774迫使激活复制(CDC45)和 G2-M 进展(PLK1 和 CCNB1)的蛋白质表达。特别是,叉保护复合物蛋白(TIMESLESS 和 TIPIN)被富集。低剂量的 M1774与包括拓扑异构酶 1 抑制剂(SN-38/伊立替康、拓扑替康、依立替康和依立替康)、拓扑异构酶 2 抑制剂依托泊苷、顺铂、RNA 聚合酶 II 抑制剂卢比尼内汀和 PARP 抑制剂他拉唑帕尼在内的广谱临床 DDA 在各种模型中具有高度协同作用,包括癌细胞系、患者来源的类器官和小鼠异种移植模型。此外,我们证明 M1774 可以逆转缺乏 SLFN11 表达的癌细胞对抗癌 DDA 的耐药性,这表明 SLFN11 可用于即将进行的临床试验中的患者选择。