Collins Victor J, Ludwig Katelyn R, Nelson Ariana E, Sundara Rajan Soumya, Yeung Choh, Vulikh Ksenia, Isanogle Kristine A, Mendoza Arnulfo, Difilippantonio Simone, Karim Baktiar O, Caplen Natasha J, Heske Christine M
Translational Sarcoma Biology Section, Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Functional Genetics Section, Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Mol Cancer Ther. 2024 Aug 1;23(8):1109-1123. doi: 10.1158/1535-7163.MCT-23-0641.
Disruption of DNA damage repair via impaired homologous recombination is characteristic of Ewing sarcoma (EWS) cells. We hypothesize that this disruption results in increased reliance on nonhomologous end joining to repair DNA damage. In this study, we investigated if pharmacologic inhibition of the enzyme responsible for nonhomologous end joining, the DNA-PK holoenzyme, alters the response of EWS cells to genotoxic standard of care chemotherapy. We used analyses of cell viability and proliferation to investigate the effects of clinical DNA-PK inhibitors (DNA-PKi) in combination with six therapeutic or experimental agents for EWS. We performed calculations of synergy using the Loewe additivity model. Immunoblotting evaluated treatment effects on DNA-PK, DNA damage, and apoptosis. Flow cytometric analyses evaluated effects on cell cycle and fate. We used orthotopic xenograft models to interrogate tolerability, drug mechanism, and efficacy in vivo. DNA-PKi demonstrated on-target activity, reducing phosphorylated DNA-PK levels in EWS cells. DNA-PKi sensitized EWS cell lines to agents that function as topoisomerase 2 (TOP2) poisons and enhanced the DNA damage induced by TOP2 poisons. Nanomolar concentrations of single-agent TOP2 poisons induced G2M arrest and little apoptotic response while adding DNA-PKi-mediated apoptosis. In vivo, the combination of AZD7648 and etoposide had limited tolerability but resulted in enhanced DNA damage, apoptosis, and EWS tumor shrinkage. The combination of DNA-PKi with standard of care TOP2 poisons in EWS models is synergistic, enhances DNA damage and cell death, and may form the basis of a promising future therapeutic strategy for EWS.
通过受损的同源重组破坏DNA损伤修复是尤因肉瘤(EWS)细胞的特征。我们假设这种破坏导致对非同源末端连接修复DNA损伤的依赖性增加。在本研究中,我们调查了对负责非同源末端连接的酶(DNA-PK全酶)的药理学抑制是否会改变EWS细胞对基因毒性标准护理化疗的反应。我们使用细胞活力和增殖分析来研究临床DNA-PK抑制剂(DNA-PKi)与六种治疗性或实验性EWS药物联合使用的效果。我们使用Loewe加和模型进行协同作用计算。免疫印迹评估了对DNA-PK、DNA损伤和细胞凋亡的治疗效果。流式细胞术分析评估了对细胞周期和命运的影响。我们使用原位异种移植模型来研究体内的耐受性、药物机制和疗效。DNA-PKi表现出靶向活性,降低了EWS细胞中磷酸化DNA-PK的水平。DNA-PKi使EWS细胞系对作为拓扑异构酶2(TOP2)毒物起作用的药物敏感,并增强了TOP2毒物诱导的DNA损伤。纳摩尔浓度的单药TOP2毒物诱导G2M期阻滞且几乎没有凋亡反应,而添加DNA-PKi则介导凋亡。在体内,AZD7648和依托泊苷的联合耐受性有限,但导致DNA损伤、细胞凋亡增强以及EWS肿瘤缩小。在EWS模型中,DNA-PKi与标准护理TOP2毒物的联合具有协同作用,增强了DNA损伤和细胞死亡,可能为EWS未来有前景的治疗策略奠定基础。