Zhu Ziqi, Shi Yujun
Department of Pathology & Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.
Key Laboratory of Transplant Engineering and Immunology, NHC, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.
Chin Med J (Engl). 2025 Mar 20;138(6):634-650. doi: 10.1097/CM9.0000000000003471. Epub 2025 Feb 11.
Poly(ADP-ribose) polymerase (PARP) inhibitors (PARPis) have emerged as critical agents for cancer therapy. By inhibiting the catalytic activity of PARP enzymes and trapping them in the DNA, PARPis disrupt DNA repair, ultimately leading to cell death, particularly in cancer cells with homologous recombination repair deficiencies, such as those harboring BRCA mutations. This review delves into the mechanisms of action of PARPis in anticancer treatments, including the inhibition of DNA repair, synthetic lethality, and replication stress. Furthermore, the clinical applications of PARPis in various cancers and their adverse effects as well as their combinations with other therapies and the mechanisms underlying resistance are summarized. This review provides comprehensive insights into the role and mechanisms of PARP and PARPis in DNA repair, with a particular focus on the potential of PARPi-based therapies in precision medicine for cancer treatment.
聚(ADP - 核糖)聚合酶(PARP)抑制剂(PARPis)已成为癌症治疗的关键药物。通过抑制PARP酶的催化活性并将其捕获在DNA中,PARPis破坏DNA修复,最终导致细胞死亡,特别是在具有同源重组修复缺陷的癌细胞中,例如那些携带BRCA突变的细胞。本文综述深入探讨了PARPis在抗癌治疗中的作用机制,包括对DNA修复的抑制、合成致死性和复制应激。此外,还总结了PARPis在各种癌症中的临床应用、它们的不良反应以及与其他疗法的联合应用及其耐药机制。本文综述全面深入地探讨了PARP和PARPis在DNA修复中的作用和机制,特别关注基于PARPi的疗法在癌症精准治疗中的潜力。