Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Fuzhou, 350207, P. R. China.
Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, 117585, Singapore.
Adv Mater. 2024 Jun;36(25):e2401017. doi: 10.1002/adma.202401017. Epub 2024 Apr 10.
Glycolysis-dominant metabolic pathway in cancer cells can promote their therapeutic resistance against radiotherapy (RT). Carbon monoxide (CO) as a glycolysis inhibitor can enhance the efficiency of RT. Herein, an X-ray responsive CO-releasing nanocomposite (HA@AuNC@CO) based on strong host-guest interactions between the radiosensitizer and CO donor for enhanced RT is developed. The encapsulated gold nanoclusters (CD-AuNCs) can effectively generate cytotoxic reactive oxygen species (ROS) under X-ray radiation, which not only directly inactivate cancer cells but also induce in situ CO gas generation from adamantane modified metal carbonyl (Ada-CO) for glycolysis inhibition. Both in vitro and in vivo results demonstrate that HA@AuNC@CO exhibits active targeting toward CD44 overexpressed cancer cells, along with excellent inhibition of glycolysis and efficient RT against cancer. This study offers a new strategy for the combination of gas therapy and RT in tumor treatment.
癌细胞中糖酵解主导的代谢途径可以促进其对放射治疗(RT)的治疗抵抗。一氧化碳(CO)作为一种糖酵解抑制剂,可以提高 RT 的效率。本文开发了一种基于 X 射线响应的 CO 释放纳米复合材料(HA@AuNC@CO),该复合材料基于放射增敏剂与 CO 供体之间的强主客体相互作用,用于增强 RT。封装的金纳米团簇(CD-AuNCs)可以在 X 射线辐射下有效产生细胞毒性活性氧(ROS),不仅可以直接灭活癌细胞,还可以从金刚烷修饰的金属羰基化合物(Ada-CO)原位产生 CO 气体以抑制糖酵解。体外和体内结果均表明,HA@AuNC@CO 对 CD44 过表达的癌细胞具有主动靶向作用,同时有效抑制糖酵解并高效进行 RT 治疗癌症。该研究为气体治疗与 RT 在肿瘤治疗中的联合提供了一种新策略。