CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France; Center for Education and Research on Macromolecules (CERM), CESAM Research Unit, University of Liege, B6a Sart-Tilman, B-4000 Liege, Belgium.
Centre Régional de Pharmacovigilance, Laboratoire de Pharmacologie-Toxicologie, CHU Angers, 4 rue Larrey, F-49100 Angers, France.
Trends Pharmacol Sci. 2019 May;40(5):342-357. doi: 10.1016/j.tips.2019.03.003. Epub 2019 Apr 9.
Although old molecules, alkylating agents and platinum derivatives are still widely used in the treatment of various solid tumors. However, systemic toxicity and cellular resistance mechanisms impede their efficacy. Innovative strategies, including local administration, optimization of treatment schedule/dosage, synergistic combinations, and the encapsulation of bioactive molecules in smart, multifunctional drug delivery systems, have shown promising results in potentiating anticancer activity while circumventing such hurdles. Furthermore, questioning of the old paradigm according to which nuclear DNA is the critical target of their anticancer activity has shed light on subcellular alternative and neglected targets that obviously participate in the mediation of cytotoxicity or resistance. Thus, rethinking of the use of these pivotal antineoplastic agents appears critical to improve clinical outcomes in the management of solid tumors.
尽管烷化剂和铂类衍生物等传统小分子药物仍广泛用于治疗各种实体瘤,但由于其全身毒性和细胞耐药机制,限制了其疗效。创新策略,包括局部给药、优化治疗方案/剂量、联合治疗以及将生物活性分子封装在智能多功能药物递送系统中,已显示出在增强抗癌活性的同时克服这些障碍的潜力。此外,人们对传统观点提出质疑,即核 DNA 是其抗癌活性的关键靶标,这揭示了亚细胞替代靶标和被忽视的靶标,这些靶标显然参与了细胞毒性或耐药性的调节。因此,重新思考这些关键的抗肿瘤药物的应用对于改善实体瘤的临床治疗结果至关重要。