Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P. R. China.
Angew Chem Int Ed Engl. 2020 Jan 27;59(5):1897-1905. doi: 10.1002/anie.201912574. Epub 2019 Dec 9.
Photodynamic therapy (PDT) has extraordinary promise for the treatment of many cancers. However, its clinical progress is impaired by the intrinsic hypoxic tumor microenvironment that limits PDT efficacy and the safety concern associated with biological specificity of photosensitizers or vehicles. Now it is demonstrated that rationally designed DNA nanosponges can load and delivery photosensitizer effectively, target tumor precisely, and relieve hypoxia-associated resistance remarkably to enhance the efficacy of PDT. Specifically, the approach exhibits a facile assembly process, provides programmable and versatile nanocarriers, and enables robust in vitro and in vivo anti-cancer efficacy with excellent biosafety. These findings represent a practical and safe approach by designer DNA nanoassemblies to combat cancer effectively and suggest a powerful strategy for broad biomedical application of PDT.
光动力疗法(PDT)在治疗多种癌症方面具有非凡的应用前景。然而,由于肿瘤内部的低氧微环境限制了 PDT 的疗效,以及与光敏剂或载体的生物特异性相关的安全性问题,其临床应用受到了阻碍。现在已经证明,经过合理设计的 DNA 纳米海绵可以有效地装载和输送光敏剂,精确靶向肿瘤,并显著缓解与缺氧相关的耐药性,从而增强 PDT 的疗效。具体来说,该方法具有简便的组装过程,提供可编程和多功能的纳米载体,并具有强大的体外和体内抗肿瘤疗效,同时具有良好的生物安全性。这些发现代表了一种通过设计 DNA 纳米组装体来有效对抗癌症的实用且安全的方法,并为 PDT 的广泛生物医学应用提供了一种强大的策略。