Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA; Center for DNA Damage and Repair, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
DNA Repair (Amst). 2018 Nov;71:172-176. doi: 10.1016/j.dnarep.2018.08.021. Epub 2018 Aug 23.
BRCA1 and BRCA2 deficient tumor cells are sensitive to inhibitors of Poly ADP Ribose Polymerase (PARP1) through the mechanism of synthetic lethality. Several PARP inhibitors, which are oral drugs and generally well tolerated, have now received FDA approval for various ovarian cancer and breast cancer indications. Despite their use in the clinic, PARP inhibitor resistance is common and develops through multiple mechanisms. Broadly speaking, BRCA1/2-deficient tumor cells can become resistant to PARP inhibitors by restoring homologous recombination (HR) repair and/or by stabilizing their replication forks. Here, we review the mechanism of PARP inhibitor resistance.
BRCA1 和 BRCA2 缺陷型肿瘤细胞对聚 ADP 核糖聚合酶(PARP1)抑制剂敏感,其作用机制为合成致死。几种 PARP 抑制剂是口服药物,通常具有良好的耐受性,现已获得 FDA 批准用于多种卵巢癌和乳腺癌适应证。尽管这些药物已在临床上应用,但 PARP 抑制剂耐药很常见,并通过多种机制产生。广义而言,BRCA1/2 缺陷型肿瘤细胞可通过恢复同源重组(HR)修复和/或稳定其复制叉而对 PARP 抑制剂产生耐药性。在此,我们综述 PARP 抑制剂耐药的机制。