Department of Molecular Oncology, British Columbia Cancer Research Centre, and Department of Pathology and Laboratory Medicine, University of British Columbia, 675 West 10th Avenue, Vancouver, British Columbia, Canada V5Z 1L3.
Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK.
Nat Commun. 2017 Feb 17;8:14432. doi: 10.1038/ncomms14432.
G-quadruplex DNAs form four-stranded helical structures and are proposed to play key roles in different cellular processes. Targeting G-quadruplex DNAs for cancer treatment is a very promising prospect. Here, we show that CX-5461 is a G-quadruplex stabilizer, with specific toxicity against BRCA deficiencies in cancer cells and polyclonal patient-derived xenograft models, including tumours resistant to PARP inhibition. Exposure to CX-5461, and its related drug CX-3543, blocks replication forks and induces ssDNA gaps or breaks. The BRCA and NHEJ pathways are required for the repair of CX-5461 and CX-3543-induced DNA damage and failure to do so leads to lethality. These data strengthen the concept of G4 targeting as a therapeutic approach, specifically for targeting HR and NHEJ deficient cancers and other tumours deficient for DNA damage repair. CX-5461 is now in advanced phase I clinical trial for patients with BRCA1/2 deficient tumours (Canadian trial, NCT02719977, opened May 2016).
G-四链体 DNA 形成四链螺旋结构,据推测在多种细胞过程中发挥关键作用。针对 G-四链体 DNA 进行癌症治疗是一个极具前景的方向。在此,我们证明 CX-5461 是一种 G-四链体稳定剂,对癌症细胞中的 BRCA 缺陷以及多克隆患者来源异种移植模型具有特异性毒性,包括对 PARP 抑制有抗性的肿瘤。CX-5461 和其相关药物 CX-3543 的暴露会阻断复制叉,并诱导单链 DNA 缺口或断裂。BRCA 和 NHEJ 通路对于修复 CX-5461 和 CX-3543 诱导的 DNA 损伤是必需的,而无法进行修复则会导致细胞死亡。这些数据强化了 G4 靶向作为一种治疗方法的概念,特别是针对 HR 和 NHEJ 缺陷型癌症以及其他 DNA 损伤修复缺陷型肿瘤。CX-5461 目前正在进行针对 BRCA1/2 缺陷型肿瘤患者的 I 期临床试验(加拿大试验,NCT02719977,2016 年 5 月开启)。