Department of Chemistry and Biochemistry, Faculty of Agronomy, Mendel University in Brno, Zemedelska 1, CZ-613 00 Brno, Czech Republic.
Pharmacol Ther. 2012 Jan;133(1):26-39. doi: 10.1016/j.pharmthera.2011.07.006. Epub 2011 Aug 3.
Over the past forty years, anthracyclines and ellipticines have attracted attention as promising cytostatics. In this review, we focus on their mechanisms of cytoxicity, DNA-damaging effects and adverse side-effects. We also summarize ways to enhance the therapeutic effects of these drugs together with a decrease in their adverse effects. Current drug design strategies are focused on drug bioavailability and their tissue targeting, whereas drug delivery to specific intracellular compartments is rarely addressed. Therefore, therapies utilizing the antineoplastic activities of anthracyclines and ellipticines combined with novel strategies such as nanotechnologies for safer drug delivery, as well as strategies based on gene therapy, could significantly contribute to medical practice.
在过去的四十年中,蒽环类药物和椭圆环类药物作为有前途的细胞抑制剂引起了人们的关注。在这篇综述中,我们重点介绍了它们的细胞毒性、DNA 损伤作用和不良反应的机制。我们还总结了提高这些药物治疗效果同时降低不良反应的方法。目前的药物设计策略集中在药物的生物利用度和组织靶向性上,而很少涉及药物递送到特定的细胞内隔室。因此,将蒽环类药物和椭圆环类药物的抗肿瘤活性与新的策略(如纳米技术用于更安全的药物递送)以及基于基因治疗的策略相结合的治疗方法,可能会对医学实践做出重大贡献。