Viera Talysa, Abfalterer Quinn, Neal Alyssa, Trujillo Richard, Patidar Praveen L
Department of Chemistry, New Mexico Institute of Mining and Technology, Socorro, NM 87801, USA.
Cancers (Basel). 2024 Jan 30;16(3):595. doi: 10.3390/cancers16030595.
R-loops (RNA-DNA hybrids with displaced single-stranded DNA) have emerged as a potent source of DNA damage and genomic instability. The termination of defective RNA polymerase II (RNAPII) is one of the major sources of R-loop formation. 5'-3'-exoribonuclease 2 (XRN2) promotes genome-wide efficient RNAPII termination, and XRN2-deficient cells exhibit increased DNA damage emanating from elevated R-loops. Recently, we showed that DNA damage instigated by XRN2 depletion in human fibroblast cells resulted in enhanced poly(ADP-ribose) polymerase 1 (PARP1) activity. Additionally, we established a synthetic lethal relationship between XRN2 and PARP1. However, the underlying cellular stress response promoting this synthetic lethality remains elusive. Here, we delineate the molecular consequences leading to the synthetic lethality of XRN2-deficient cancer cells induced by PARP inhibition. We found that XRN2-deficient lung and breast cancer cells display sensitivity to two clinically relevant PARP inhibitors, Rucaparib and Olaparib. At a mechanistic level, PARP inhibition combined with XRN2 deficiency exacerbates R-loop and DNA double-strand break formation in cancer cells. Consistent with our previous findings using several different siRNAs, we also show that XRN2 deficiency in cancer cells hyperactivates PARP1. Furthermore, we observed enhanced replication stress in XRN2-deficient cancer cells treated with PARP inhibitors. Finally, the enhanced stress response instigated by compromised PARP1 catalytic function in XRN2-deficient cells activates caspase-3 to initiate cell death. Collectively, these findings provide mechanistic insights into the sensitivity of XRN2-deficient cancer cells to PARP inhibition and strengthen the underlying translational implications for targeted therapy.
R环(带有单链DNA置换的RNA-DNA杂交体)已成为DNA损伤和基因组不稳定的一个重要来源。缺陷型RNA聚合酶II(RNAPII)的终止是R环形成的主要来源之一。5'-3'-外切核糖核酸酶2(XRN2)促进全基因组范围内RNAPII的有效终止,而XRN2缺陷的细胞会因R环升高而表现出DNA损伤增加。最近,我们发现人成纤维细胞中XRN2缺失引发的DNA损伤导致聚(ADP-核糖)聚合酶1(PARP1)活性增强。此外,我们还确立了XRN2与PARP1之间的合成致死关系。然而,促进这种合成致死性的潜在细胞应激反应仍不清楚。在此,我们阐述了PARP抑制诱导的XRN2缺陷癌细胞合成致死性的分子后果。我们发现XRN2缺陷的肺癌和乳腺癌细胞对两种临床相关的PARP抑制剂鲁卡帕尼和奥拉帕尼敏感。在机制层面,PARP抑制与XRN2缺陷相结合会加剧癌细胞中R环和DNA双链断裂的形成。与我们之前使用几种不同小干扰RNA的研究结果一致,我们还表明癌细胞中XRN2缺陷会过度激活PARP1。此外,我们观察到用PARP抑制剂处理的XRN2缺陷癌细胞中复制应激增强。最后,XRN2缺陷细胞中PARP1催化功能受损引发的应激反应增强激活了半胱天冬酶-3以启动细胞死亡。总的来说,这些发现为XRN2缺陷癌细胞对PARP抑制的敏感性提供了机制性见解,并加强了对靶向治疗的潜在转化意义。