School of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, Republic of Korea.
Adv Healthc Mater. 2013 Sep;2(9):1252-8. doi: 10.1002/adhm.201200471. Epub 2013 Mar 14.
The majority of anticancer therapeutics have failed to control the target cancers. Thus, new rational design concepts are critical. In most of the biological reactions, a cascade pathway is used to activate appropriate responses. In the cascade pathway, a small signal derived from neighboring environments can be amplified and it further triggers overwhelming and specialized responses. It can be applied to achieve powerful therapeutic effects for novel drug design strategies. Inspired by this concept, we design a preferential dual anti-cancer therapeutic cassette composed of (i) DNA/RNA nanostructures as both anticancer containers and target ligands and (ii) a gold nanocrystal as localized heat inducers. We demonstrate that this multi-modular platform is superior to conventional cancer medications in that it had higher drug loading efficiency, tunable drug release, and intrinsic serum stability characteristics. Both doxorubicin chemotherapy and thermal ablation exert a powerful synergistic killing effect that resulted in prostate cancer regression both in vitro and in vivo. We speculate that our novel anti-cancer drug system can be adapted to effectively destroy many different types of solid cancers.
大多数抗癌疗法都未能控制目标癌症。因此,新的合理设计理念至关重要。在大多数生物反应中,级联途径用于激活适当的反应。在级联途径中,源自邻近环境的小信号可以被放大,并且它进一步引发压倒性的和专门的反应。它可以应用于实现新型药物设计策略的强大治疗效果。受此概念的启发,我们设计了一种优先的双重抗癌治疗盒,由 (i) DNA/RNA 纳米结构作为抗癌容器和靶配体和 (ii) 金纳米晶体作为局部热诱导剂组成。我们证明,与传统的癌症药物相比,这种多模块平台具有更高的药物负载效率、可调药物释放和内在的血清稳定性特征。多柔比星化疗和热消融都发挥了强大的协同杀伤作用,导致体外和体内前列腺癌消退。我们推测,我们的新型抗癌药物系统可以适应有效地破坏许多不同类型的实体癌。