Translational Innovation Platform Oncology, EMD Serono Research and Development Institute, Inc., Billerica, Massachusetts.
Translational Innovation Platform Oncology, Biopharma Research and Development, Merck KGaA, Darmstadt, Germany.
Mol Cancer Res. 2019 Dec;17(12):2457-2468. doi: 10.1158/1541-7786.MCR-19-0362. Epub 2019 Sep 24.
Inhibition of DNA double-strand break (DSB) repair in cancer cells has been proposed as a new therapeutic strategy for potentiating the anticancer effects of radiotherapy. M3814 is a novel, selective pharmacologic inhibitor of the serine/threonine kinase DNA-dependent protein kinase (DNA-PK), a key driver of nonhomologous end-joining, one of the main DSB-repair pathways, currently under clinical investigation. Here, we show that M3814 effectively blocks the repair of radiation-induced DSBs and potently enhances p53 phosphorylation and activation. In p53 wild-type cells, ataxia telangiectasia-mutated (ATM) and its targets, p53 and checkpoint kinase 2 (CHK2), were more strongly activated by combination treatment with M3814 and radiation than by radiation alone, leading to a complete p53-dependent cell-cycle block and premature cell senescence. Cancer cells with dysfunctional p53 were unable to fully arrest their cell cycle and entered S and M phases with unrepaired DNA, leading to mitotic catastrophe and apoptotic cell death. Isogenic p53-null/wild-type A549 and HT-1080 cell lines were generated and used to demonstrate that p53 plays a critical role in determining the response to ionizing radiation and M3814. Time-lapse imaging of cell death and measuring apoptosis in panels of p53 wild-type and p53-null/mutant cancer lines confirmed the clear differences in cell fate, dependent on p53 status. IMPLICATIONS: Our results identify p53 as a possible biomarker for response of cancer cells to combination treatment with radiation and a DNA-PK inhibitor and suggest that p53 mutation status should be considered in the design of future clinical trials. VISUAL OVERVIEW: http://mcr.aacrjournals.org/content/molcanres/17/12/2457/F1.large.jpg.
抑制癌细胞中的 DNA 双链断裂(DSB)修复被提议作为一种新的治疗策略,以增强放疗的抗癌效果。M3814 是一种新型、选择性的丝氨酸/苏氨酸激酶 DNA 依赖性蛋白激酶(DNA-PK)的药理学抑制剂,是非同源末端连接的关键驱动因素之一,也是目前正在临床研究中的主要 DSB 修复途径之一。在这里,我们表明 M3814 能有效地阻断辐射诱导的 DSB 的修复,并能有效地增强 p53 的磷酸化和激活。在 p53 野生型细胞中,共济失调毛细血管扩张突变(ATM)及其靶点 p53 和检查点激酶 2(CHK2)在与 M3814 和辐射联合治疗时比单独辐射更强烈地被激活,导致完全依赖于 p53 的细胞周期阻滞和过早的细胞衰老。p53 功能失调的癌细胞不能完全阻止其细胞周期,并且带着未修复的 DNA 进入 S 和 M 期,导致有丝分裂灾难和凋亡细胞死亡。生成了具有功能失调的 p53 的同源缺失/p53 野生型 A549 和 HT-1080 细胞系,并用于证明 p53 在决定对电离辐射和 M3814 的反应中起着关键作用。对细胞死亡的延时成像和对 p53 野生型和 p53 缺失/突变型癌细胞系的细胞凋亡的测量证实了细胞命运的明显差异,这取决于 p53 的状态。意义:我们的结果确定了 p53 作为癌症细胞对放射治疗和 DNA-PK 抑制剂联合治疗的反应的一个可能的生物标志物,并建议在未来临床试验的设计中应考虑 p53 突变状态。直观描述:http://mcr.aacrjournals.org/content/molcanres/17/12/2457/F1.large.jpg。