Jette Nicholas R, Kumar Mehul, Radhamani Suraj, Arthur Greydon, Goutam Siddhartha, Yip Steven, Kolinsky Michael, Williams Gareth J, Bose Pinaki, Lees-Miller Susan P
Department of Biochemistry and Molecular Biology, Robson DNA Science Centre, Charbonneau Cancer Institute, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 1N4, Canada.
Tom Baker Cancer Centre, 1331 29 St NW, Calgary, AB T2N 4N2, Canada.
Cancers (Basel). 2020 Mar 14;12(3):687. doi: 10.3390/cancers12030687.
Poly-ADP ribose polymerase (PARP) inhibitors are currently used in the treatment of several cancers carrying mutations in the breast and ovarian cancer susceptibility genes and , with many more potential applications under study and in clinical trials. Here, we discuss the potential for extending PARP inhibitor therapies to tumours with deficiencies in the DNA damage-activated protein kinase, Ataxia-Telangiectasia Mutated (ATM). We highlight our recent findings that PARP inhibition alone is cytostatic but not cytotoxic in ATM-deficient cancer cells and that the combination of a PARP inhibitor with an ATR (ATM, Rad3-related) inhibitor is required to induce cell death.
聚(ADP-核糖)聚合酶(PARP)抑制剂目前用于治疗携带乳腺癌和卵巢癌易感基因 突变的多种癌症,并且还有更多潜在应用正在研究和临床试验中。在这里,我们讨论将PARP抑制剂疗法扩展至DNA损伤激活蛋白激酶共济失调毛细血管扩张突变(ATM)存在缺陷的肿瘤的可能性。我们强调我们最近的发现,即单独的PARP抑制在ATM缺陷癌细胞中具有细胞生长抑制作用但无细胞毒性,并且需要将PARP抑制剂与ATR(ATM,Rad3相关)抑制剂联合使用才能诱导细胞死亡。