Division of Experimental Oncology, Department of Oncology, Faculty of Medicine & Dentistry, University of Alberta, 11560 University Avenue, Edmonton, AB T6G 1Z2, Canada.
Department of Biophysics, Faculty of Science, Cairo University, Giza 12613, Egypt.
Cells. 2023 Jul 21;12(14):1904. doi: 10.3390/cells12141904.
Detailing the connection between homeostatic functions of enzymatic families and eventual progression into tumorigenesis is crucial to our understanding of anti-cancer therapies. One key enzyme group involved in this process is the Poly (ADP-ribose) polymerase (PARP) family, responsible for an expansive number of cellular functions, featuring members well established as regulators of DNA repair, genomic stability and beyond. Several PARP inhibitors (PARPi) have been approved for clinical use in a range of cancers, with many more still in trials. Unfortunately, the occurrence of resistance to PARPi therapy is growing in prevalence and requires the introduction of novel counter-resistance mechanisms to maintain efficacy. In this review, we summarize the updated understanding of the vast homeostatic functions the PARP family mediates and pin the importance of PARPi therapies as anti-cancer agents while discussing resistance mechanisms and current up-and-coming counter-strategies for countering such resistance.
详细描述酶家族的动态平衡功能与最终肿瘤发生之间的关系,对于我们理解抗癌疗法至关重要。在这个过程中涉及的一个关键酶组是聚(ADP-核糖)聚合酶(PARP)家族,它负责许多细胞功能,其成员被广泛认为是 DNA 修复、基因组稳定性等的调节剂。几种 PARP 抑制剂(PARPi)已被批准用于多种癌症的临床应用,还有许多仍在临床试验中。不幸的是,对 PARPi 治疗的耐药性越来越普遍,需要引入新的抗耐药机制来维持疗效。在这篇综述中,我们总结了 PARP 家族介导的广泛动态平衡功能的最新认识,并强调了 PARPi 治疗作为抗癌药物的重要性,同时讨论了耐药机制以及目前针对这种耐药性的新兴对抗策略。