Department of Radiation Oncology, University of Michigan Medical School, Ann Arbor, Michigan.
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan.
Mol Cancer Ther. 2021 Feb;20(2):263-273. doi: 10.1158/1535-7163.MCT-20-0365. Epub 2020 Dec 2.
PARP inhibitor monotherapy (olaparib) was recently FDA approved for the treatment of BRCA1/2-mutant, homologous recombination (HR) repair-deficient pancreatic cancer. Most pancreatic cancers, however, are HR proficient and thus resistant to PARP inhibitor monotherapy. We tested the hypothesis that combined therapy with radiation and ataxia telangiectasia and Rad3-related (ATR) inhibitor (AZD6738) would extend the therapeutic indication of olaparib to HR-proficient pancreatic cancers. We show that olaparib combined with AZD6738 significantly reduced radiation survival relative to either agent alone, regardless of HR status. Whereas catalytic inhibition of PARP with low concentrations of olaparib radiosensitized HR-deficient models, maximal sensitization in HR-proficient models required concentrations of olaparib that induce formation of PARP1-DNA complexes. Furthermore, CRISPR-Cas9-mediated PARP1 deletion failed to recapitulate the effects of olaparib on radiosensitivity and negated the combinatorial efficacy of olaparib and AZD6738 on radiosensitization, suggesting that PARP1-DNA complexes, rather than PARP catalytic inhibition, were responsible for radiosensitization. Mechanistically, therapeutic concentrations of olaparib in combination with radiation and AZD6738 increased DNA double-strand breaks. DNA fiber combing revealed that high concentrations of olaparib did not stall replication forks but instead accelerated replication fork progression in association with an ATR-mediated replication stress response that was antagonized by AZD6738. Finally, in HR-proficient tumor xenografts, the combination of olaparib, radiation, and AZD6738 significantly delayed tumor growth compared with all other treatments. These findings suggest that PARP1-DNA complexes are required for the therapeutic activity of olaparib combined with radiation and ATR inhibitor in HR-proficient pancreatic cancer and support the clinical development of this combination for tumors intrinsically resistant to PARP inhibitors.
聚 ADP 核糖聚合酶(PARP)抑制剂单药(奥拉帕尼)最近被美国食品和药物管理局(FDA)批准用于治疗 BRCA1/2 突变、同源重组(HR)修复缺陷型胰腺癌。然而,大多数胰腺癌 HR 功能正常,因此对 PARP 抑制剂单药治疗具有抗性。我们检验了这样一种假设,即联合放疗和共济失调毛细血管扩张症和 Rad3 相关(ATR)抑制剂(AZD6738)治疗将奥拉帕尼的治疗适应证扩展到 HR 功能正常的胰腺癌。我们发现,奥拉帕尼联合 AZD6738 与单独使用任一药物相比,均显著降低了放疗后的存活率,而与 HR 状态无关。虽然用低浓度的奥拉帕尼催化抑制 PARP 可使 HR 缺陷型模型对放疗敏感,但在 HR 功能正常的模型中,最大的增敏作用需要诱导 PARP1-DNA 复合物形成的奥拉帕尼浓度。此外,CRISPR-Cas9 介导的 PARP1 缺失未能重现奥拉帕尼对放疗敏感性的影响,并否定了奥拉帕尼和 AZD6738 联合放疗增敏的组合疗效,这表明 PARP1-DNA 复合物而不是 PARP 催化抑制,是放疗增敏的原因。从机制上讲,奥拉帕尼联合放疗和 AZD6738 的治疗浓度增加了 DNA 双链断裂。DNA 纤维梳理揭示,高浓度的奥拉帕尼不会使复制叉停滞,而是加速复制叉的进展,与 ATR 介导的复制应激反应相关,该反应被 AZD6738 拮抗。最后,在 HR 功能正常的肿瘤异种移植中,与其他所有治疗方法相比,奥拉帕尼、放疗和 AZD6738 的联合治疗显著延迟了肿瘤生长。这些发现表明,PARP1-DNA 复合物是奥拉帕尼联合放疗和 ATR 抑制剂在 HR 功能正常的胰腺癌中发挥治疗活性所必需的,并支持该联合疗法用于对 PARP 抑制剂固有耐药的肿瘤的临床开发。