Department of Chemistry, City University of Hong Kong, Hong Kong SAR, P. R. China.
Dalton Trans. 2019 Feb 19;48(8):2536-2544. doi: 10.1039/c8dt03923b.
Cisplatin plays a pivotal role in the treatment of various malignant tumors, but its therapeutic effects are hampered by drug resistance. Pt(iv) prodrugs represent a promising class of "non-conventional" platinum-based anticancer agents to circumvent drug resistance, which can be easily functionalized with other bioactive ligands. One strategy is to build "dual-action" and "multi-action" Pt(iv) prodrugs that not only damage DNA but also perturb other pathways related to cisplatin resistance to achieve combinatorial therapeutic effects. Another way to overcome the shortcomings of cisplatin is to deliver Pt(iv) prodrugs via nanocarriers. Most studies in this area have focused on designing prodrugs based on the mechanism of cisplatin resistance within isolated cancer cells. Recent findings, however, reveal that the tumor microenvironment also plays important roles in the development of cisplatin resistance. This perspective focuses on various types of novel cisplatin-based Pt(iv) complexes, including Pt-loaded nanostructures, to overcome cisplatin resistance. Special attention will be devoted to complexes that target the tumor microenvironment, which is a new area for the development of effective Pt(iv) prodrugs. Our summary and outlook may have a hope to help researchers in the field generate new ideas and strategies to develop more potent Pt(iv) prodrugs to combat cisplatin resistance.
顺铂在多种恶性肿瘤的治疗中发挥着关键作用,但由于耐药性的存在,其治疗效果受到了限制。Pt(iv)前药是一类很有前途的“非传统”铂类抗癌药物,可以克服耐药性,并且可以很容易地与其他生物活性配体进行功能化。一种策略是构建“双重作用”和“多作用”Pt(iv)前药,不仅可以破坏 DNA,还可以扰乱与顺铂耐药性相关的其他途径,从而实现联合治疗效果。克服顺铂缺点的另一种方法是通过纳米载体来输送 Pt(iv)前药。该领域的大多数研究都集中在基于单个癌细胞中顺铂耐药机制来设计前药。然而,最近的发现表明,肿瘤微环境在顺铂耐药性的发展中也起着重要作用。本综述重点介绍了各种新型基于顺铂的 Pt(iv)配合物,包括负载 Pt 的纳米结构,以克服顺铂耐药性。特别关注针对肿瘤微环境的配合物,这是开发有效 Pt(iv)前药的新领域。我们的总结和展望有望帮助该领域的研究人员产生新的想法和策略,以开发更有效的 Pt(iv)前药来对抗顺铂耐药性。