Hefei National Laboratory for Physical Sciences at the Microscale , University of Science and Technology of China , Hefei 230027 , China.
Breast Tumor Center , Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University , Guangzhou 510120 , China.
ACS Nano. 2018 Jun 26;12(6):5684-5698. doi: 10.1021/acsnano.8b01508. Epub 2018 Jun 4.
Clinical success of cancer radiotherapy is usually impeded by a combination of two factors, i.e., insufficient DNA damage and rapid DNA repair during and after treatment, respectively. Existing strategies for optimizing the radiotherapeutic efficacy often focus on only one facet of the issue, which may fail to function in the long term trials. Herein, we report a DNA-dual-targeting approach for enhanced cancer radiotherapy using a hierarchical multiplexing nanodroplet, which can simultaneously promote DNA lesion formation and prevent subsequent DNA damage repair. Specifically, the ultrasmall gold nanoparticles encapsulated in the liquid nanodroplets can concentrate the radiation energy and induce dramatic DNA damage as evidenced by the enhanced formation of γ-H2AX foci as well as in vivo tumor growth inhibition. Additionally, the ultrasound-triggered burst release of oxygen may relieve tumor hypoxia and fix the DNA radical intermediates produced by ionizing radiation, prevent DNA repair, and eventually result in cancer death. Finally, the nanodroplet platform is compatible with fluorescence, ultrasound, and magnetic resonance imaging techniques, allowing for real-time in vivo imaging-guided precision radiotherapy in an EMT-6 tumor model with significantly enhanced treatment efficacy. Our DNA-dual-targeting design of simultaneously enhancing DNA damage and preventing DNA repair presents an innovative strategy to effective cancer radiotherapy.
癌症放射治疗的临床疗效通常受到两个因素的阻碍,分别是治疗过程中和治疗后分别存在的 DNA 损伤不足和快速修复。现有的优化放射治疗效果的策略通常仅关注问题的一个方面,这在长期试验中可能无法发挥作用。在此,我们报告了一种使用分级复用纳米液滴增强癌症放射治疗的 DNA 双重靶向方法,该方法可以同时促进 DNA 损伤形成并阻止随后的 DNA 损伤修复。具体而言,包裹在液滴中的超小金纳米颗粒可以集中辐射能量,并通过增强 γ-H2AX 焦点的形成以及体内肿瘤生长抑制来证明其诱导了剧烈的 DNA 损伤。此外,超声触发的氧气爆发释放可以缓解肿瘤缺氧,并固定由电离辐射产生的 DNA 自由基中间体,阻止 DNA 修复,最终导致癌细胞死亡。最后,纳米液滴平台与荧光、超声和磁共振成像技术兼容,允许在 EMT-6 肿瘤模型中进行实时体内成像引导的精确放射治疗,并显著提高治疗效果。我们的同时增强 DNA 损伤和防止 DNA 修复的 DNA 双重靶向设计为有效的癌症放射治疗提供了一种创新策略。