Ngo Greg, Hyatt Sam, Grimstead Julia, Jones Rhiannon, Hendrickson Eric, Pepper Chris, Baird Duncan
Division of Cancer and Genetics, School of Medicine, Cardiff University, Heath Park, Cardiff, UK.
Department of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Minneapolis, MN, USA.
Oncotarget. 2018 Dec 25;9(101):37549-37563. doi: 10.18632/oncotarget.26499.
Telomeric crisis is the final replicative barrier to cell immortalisation; it is characterised by genome instability and cell death and is triggered when telomeres become critically short and are subjected to fusion. Pre-cancerous lesions, or early stage cancers, often show signs of a telomere crisis, suggesting that escape from telomere crisis is a prerequisite for disease progression. Telomeric crisis therefore represents an attractive, and as yet unexplored, opportunity for therapeutic intervention. Here, we show that two clinically approved PARP inhibitors, selectively eliminate human cells undergoing a telomere-driven crisis. Clonal populations of a colorectal cancer cell line (HCT116), or the plasma cell leukaemia cell line (JJN-3), expressing a dominant-negative telomerase, entered a telomere-driven crisis at defined population doubling points and telomere lengths. The addition of the PARP inhibitors, olaparib or rucaparib prevented these cells from escaping crisis. PARP inhibition did not alter cellular proliferation prior to crisis, rates of telomere erosion or the telomere length at which crisis was initiated, but affected repair of eroded telomeres, resulting in an increased in intra-chromosomal telomere fusion. This was accompanied by enhanced DNA damage checkpoint activation and elevated levels of apoptosis. We propose that PARP inhibitors impair the repair of dysfunctional telomeres and/or induce replicative stress at telomeres to inhibit escape from a telomere crisis. This is the first demonstration that a drug can selectively kill cells experiencing telomeric crisis. We propose that this type of drug, which we term 'crisolytic', has the potential to eliminate pre-cancerous lesions and tumours exhibiting short dysfunctional telomeres.
端粒危机是细胞永生化的最终复制障碍;其特征是基因组不稳定和细胞死亡,当端粒变得极短并发生融合时被触发。癌前病变或早期癌症通常表现出端粒危机的迹象,这表明逃离端粒危机是疾病进展的先决条件。因此,端粒危机代表了一个有吸引力但尚未被探索的治疗干预机会。在这里,我们表明两种临床批准的PARP抑制剂能够选择性地消除经历端粒驱动危机的人类细胞。表达显性负性端粒酶的结肠癌细胞系(HCT116)或浆细胞白血病细胞系(JJN-3)的克隆群体在确定的群体倍增点和端粒长度时进入端粒驱动的危机。添加PARP抑制剂奥拉帕尼或鲁卡帕尼可阻止这些细胞逃离危机。PARP抑制在危机前不会改变细胞增殖、端粒侵蚀速率或引发危机的端粒长度,但会影响侵蚀端粒的修复,导致染色体内端粒融合增加。这伴随着DNA损伤检查点激活增强和凋亡水平升高。我们提出PARP抑制剂损害功能失调端粒的修复和/或在端粒处诱导复制应激以抑制逃离端粒危机。这是首次证明一种药物可以选择性杀死经历端粒危机的细胞。我们提出这种类型的药物,我们称之为“溶端粒药物”,有潜力消除表现出短功能失调端粒的癌前病变和肿瘤。