Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, London, UK.
J Pathol. 2013 Feb;229(3):422-9. doi: 10.1002/path.4140.
PARP inhibitors (PARPi) for the treatment of BRCA1 or BRCA2 deficient tumours are currently the focus of seminal clinical trials exploiting the concept of synthetic lethality. Although clinical resistance to PARPi has been described, the mechanism underlying this has not been elucidated. Here, we investigate tumour material from patients who had developed resistance to the PARPi olaparib, subsequent to showing an initial clinical response. Massively parallel DNA sequencing of treatment-naive and post-olaparib treatment biopsies identified tumour-specific BRCA2 secondary mutations in olaparib-resistant metastases. These secondary mutations restored full-length BRCA2 protein, and most likely cause olaparib resistance by re-establishing BRCA2 function in the tumour cells.
聚腺苷二磷酸核糖聚合酶(PARP)抑制剂(PARPi)用于治疗 BRCA1 或 BRCA2 缺陷型肿瘤,目前是利用合成致死概念进行的重要临床试验的重点。尽管已经描述了对 PARPi 的临床耐药性,但尚未阐明其潜在机制。在这里,我们研究了对 PARPi 奥拉帕利治疗产生耐药性的患者的肿瘤标本,这些患者在初始临床反应后表现出这种耐药性。对治疗前和奥拉帕利治疗后活检的大量平行 DNA 测序鉴定出奥拉帕利耐药转移灶中特定的 BRCA2 继发性突变。这些继发性突变恢复了全长 BRCA2 蛋白,并且很可能通过在肿瘤细胞中重新建立 BRCA2 功能而导致奥拉帕利耐药性。