When starvation therapy meets chemodynamic therapy

Nicholas Thomas Blum , Lianhua Fu , Jing Lin, Peng Huang
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引用次数: 3

Abstract

In recent years, starvation-primed chemodynamic therapies (ST–CDT) have become a hot topic in the wake of many discoveries related to the aberrant metabolism of cancer cells and their resistance to traditional chemotherapies, as well as altered redox signaling within tumor cells. Nanotechnology platforms are in a unique position to exploit these interrelated phenomena to realize a therapeutic effect; few therapeutic modalities are able to deliver multiple drugs simultaneously outside of nanotechnology, a basic requirement when striving to exploit a complex, interactive system such as a cancer cell. In this review, the pertinent mechanisms of ST and CDT, as well as the important interactions between these two therapies, are discussed. We outline how these therapies may work synergistically or antagonistically, depending on both the therapeutic design and the system of reactions involved. Lastly, specific applications that nanotechnology is particularly well-suited are given, which may offer improvement over clinical state-of-the-art. Such considerations are important, as nanotechnology has historically encountered great difficulty in clinical translation.

当饥饿疗法遇到化学动力疗法
近年来,饥饿引发的化学动力疗法(ST-CDT)已成为一个热门话题,因为许多发现与癌细胞的异常代谢及其对传统化疗的耐药性以及肿瘤细胞内氧化还原发信号的改变有关。纳米技术平台在利用这些相互关联的现象来实现治疗效果方面处于独特的地位;在纳米技术之外,很少有治疗方式能够同时提供多种药物,这是努力利用复杂的、相互作用的系统(如癌细胞)的基本要求。本文综述了ST和CDT的相关机制,以及这两种疗法之间的重要相互作用。我们概述了这些疗法如何协同或拮抗作用,这取决于治疗设计和所涉及的反应系统。最后,给出了纳米技术特别适合的具体应用,这可能比临床技术提供改进。这些考虑是重要的,因为纳米技术在临床转化中历来遇到了很大的困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.90
自引率
0.00%
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