School of Advanced Materials, Peking University Shenzhen Graduate School, Peking University, Shenzhen, 518055, China.
Department of Materials Science and Engineering, Southern University of Science and Technology, 1088 Xueyuan Blvd., Nanshan District, Shenzhen, Guangdong, 518055, P. R. China.
Adv Sci (Weinh). 2021 Oct;8(19):e2101467. doi: 10.1002/advs.202101467. Epub 2021 Aug 7.
Recent investigations reveal that lactate is not a waste product but a major energy source for cells, especially in the mitochondria, which can support cellular survival under glucose shortage. Accordingly, the new understanding of lactate prompts to target it together with glucose to pursue a more efficient cancer starvation therapy. Herein, zeolitic imidazolate framework-8 (ZIF-8) nanoplatforms are used to co-deliver α-cyano-4-hydroxycinnamate (CHC) and glucose oxidase (GOx) and fulfill the task of simultaneous depriving of lactate and glucose, resulting in a new nanomedicine CHC/GOx@ZIF-8. The synthesis conditions are carefully optimized in order to yield monodisperse and uniform nanomedicines, which will ensure reliable and steady therapeutic properties. Compared with the strategies aiming at a single carbon source, improved starvation therapy efficacy is observed. Besides, more than boosting the energy shortage, CHC/GOx@ZIF-8 can block the lactate-fueled respiration and relieve solid tumor hypoxia, which will enhance GOx catalysis activity, depleting extra glucose, and producing more cytotoxic H O . By the synergistically enhanced anti-tumor effect, both in vitro and in vivo cancer-killing efficacies of CHC/GOx@ZIF-8 show twice enhancements than the GOx mediated therapy. The results demonstrate that the dual-depriving of lactate and glucose is a more advanced strategy for strengthening cancer starvation therapy.
最近的研究表明,乳酸不是一种废物产物,而是细胞的主要能量来源,尤其是在细胞线粒体中,它可以在葡萄糖缺乏的情况下支持细胞存活。因此,对乳酸的新认识促使我们将其与葡萄糖一起靶向,以追求更有效的癌症饥饿治疗。在这里,沸石咪唑酯骨架-8(ZIF-8)纳米平台被用于共同递送α-氰基-4-羟基肉桂酸(CHC)和葡萄糖氧化酶(GOx),并完成同时剥夺乳酸和葡萄糖的任务,从而产生新的纳米药物 CHC/GOx@ZIF-8。仔细优化了合成条件,以产生单分散和均匀的纳米药物,这将确保可靠和稳定的治疗特性。与针对单一碳源的策略相比,观察到饥饿治疗效果得到了改善。此外,CHC/GOx@ZIF-8 不仅可以缓解能量短缺,还可以阻断乳酸供能呼吸和缓解实体瘤缺氧,从而增强 GOx 催化活性,消耗额外的葡萄糖,并产生更多的细胞毒性 H O 。通过协同增强的抗肿瘤作用,CHC/GOx@ZIF-8 在体外和体内的抗肿瘤效果都比 GOx 介导的治疗增强了两倍。结果表明,同时剥夺乳酸和葡萄糖是增强癌症饥饿治疗的更先进策略。