Department of Radiation Oncology, Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Int J Mol Sci. 2021 Jul 30;22(15):8199. doi: 10.3390/ijms22158199.
Platinum-based chemotherapies, such as cisplatin, play a large role in cancer treatment. The development of resistance and treatment toxicity creates substantial barriers to disease control, yet. To enhance the therapeutic index of cisplatin-based chemotherapy, it is imperative to circumvent resistance and toxicity while optimizing tumor sensitization. One of the primary mechanisms by which cancer cells develop resistance to cisplatin is through upregulation of DNA repair pathways. In this review, we discuss the DNA damage response in the context of cisplatin-induced DNA damage. We describe the proteins involved in the pathways and their roles in resistance development. Common biomarkers for cisplatin resistance and their utilization to improve patient risk stratification and treatment personalization are addressed. Finally, we discuss some of the current treatments and future strategies to circumvent the development of cisplatin resistance.
铂类化疗药物,如顺铂,在癌症治疗中发挥着重要作用。然而,耐药性的发展和治疗毒性对疾病控制构成了巨大的障碍。为了提高基于顺铂的化疗的治疗指数,必须规避耐药性和毒性,同时优化肿瘤敏感性。癌细胞对顺铂产生耐药性的主要机制之一是通过上调 DNA 修复途径。在这篇综述中,我们讨论了顺铂诱导的 DNA 损伤背景下的 DNA 损伤反应。我们描述了参与这些途径的蛋白质及其在耐药性发展中的作用。还讨论了顺铂耐药性的常见生物标志物及其在改善患者风险分层和治疗个体化中的应用。最后,我们讨论了一些规避顺铂耐药性发展的当前治疗方法和未来策略。