Early Oncology R&D, AstraZeneca, Gaithersburg, Maryland.
Antibody Discovery & Protein Engineering, AstraZeneca, Gaithersburg, Maryland.
Mol Cancer Ther. 2021 Mar;20(3):541-552. doi: 10.1158/1535-7163.MCT-20-0351.
Resistance to antibody-drug conjugates (ADCs) has been observed in both preclinical models and clinical studies. However, mechanisms of resistance to pyrrolobenzodiazepine (PBD)-conjugated ADCs have not been well characterized and thus, this study was designed to investigate development of resistance to PBD dimer warheads and PBD-conjugated ADCs. We established a PBD-resistant cell line, 361-PBDr, by treating human breast cancer MDA-MB-361 cells with gradually increasing concentrations of SG3199, the PBD dimer released from the PBD drug-linker tesirine. 361-PBDr cells were over 20-fold less sensitive to SG3199 compared with parental cells and were cross-resistant to other PBD warhead and ADCs conjugated with PBDs. Proteomic profiling revealed that downregulation of Schlafen family member 11 (SLFN11), a putative DNA/RNA helicase, sensitizing cancer cells to DNA-damaging agents, was associated with PBD resistance. Confirmatory studies demonstrated that siRNA knockdown of SLFN11 in multiple tumor cell lines conferred reduced sensitivity to SG3199 and PBD-conjugated ADCs. Treatment with EPZ011989, an EZH2 inhibitor, derepressed SLFN11 expression in 361-PBDr and other SLFN11-deficient tumor cells, and increased sensitivity to PBD and PBD-conjugated ADCs, indicating that the suppression of SLFN11 expression is associated with histone methylation as reported. Moreover, we demonstrated that combining an ataxia telangiectasia and Rad3-related protein (ATR) inhibitor, AZD6738, with SG3199 or PBD-based ADCs led to synergistic cytotoxicity in either resistant 361-PBDr cells or cells that SLFN11 was knocked down via siRNA. Collectively, these data provide insights into potential development of resistance to PBDs and PBD-conjugated ADCs, and more importantly, inform strategy development to overcome such resistance.
抗体药物偶联物(ADC)的耐药性已在临床前模型和临床研究中观察到。然而,针对吡咯并苯二氮卓(PBD)偶联 ADC 的耐药机制尚未得到很好的描述,因此,本研究旨在研究对 PBD 二聚体弹头和 PBD 偶联 ADC 的耐药性发展。我们通过用逐渐增加浓度的 SG3199 处理人乳腺癌 MDA-MB-361 细胞,建立了 PBD 耐药细胞系 361-PBDr,SG3199 是从 PBD 药物接头 tesirine 释放的 PBD 二聚体。与亲本细胞相比,361-PBDr 细胞对 SG3199 的敏感性降低了 20 多倍,并且对其他 PBD 弹头和与 PBD 偶联的 ADC 具有交叉耐药性。蛋白质组学分析表明,下调 Schlafen 家族成员 11(SLFN11),一种假定的 DNA/RNA 解旋酶,可使癌细胞对 DNA 损伤剂敏感,与 PBD 耐药性相关。确认研究表明,在多种肿瘤细胞系中 SLFN11 的 siRNA 敲低导致对 SG3199 和 PBD 偶联 ADC 的敏感性降低。用 EZH2 抑制剂 EPZ011989 处理可使 361-PBDr 和其他 SLFN11 缺陷型肿瘤细胞中 SLFN11 的表达去抑制,并增加对 PBD 和 PBD 偶联 ADC 的敏感性,表明抑制 SLFN11 的表达与报道的组蛋白甲基化有关。此外,我们证明,用 ataxia telangiectasia 和 Rad3 相关蛋白(ATR)抑制剂 AZD6738 联合 SG3199 或基于 PBD 的 ADCs,可在耐药的 361-PBDr 细胞或通过 siRNA 敲低 SLFN11 的细胞中导致协同细胞毒性。总之,这些数据提供了对 PBD 和 PBD 偶联 ADC 耐药性发展的深入了解,更重要的是,为克服这种耐药性的策略制定提供了信息。