化学
超氧化物歧化酶
超氧化物
活性氧
细胞内
激进的
酶
生物化学
歧化
抗氧化剂
细胞凋亡
癌细胞
衰老自由基理论
体内
细胞生物学
癌症
生物
催化作用
遗传学
生物技术
作者
Hanae Lim,Chaeun Oh,Myong‐Suk Park,Hyung-Bin Park,Chaewon Ahn,Woo Kyun Bae,Kyung Hyun Yoo,Seungwoo Hong
摘要
Superoxide dismutases (SODs) are essential antioxidant enzymes that prevent massive superoxide radical production and thus protect cells from damage induced by free radicals. However, this concept has rarely been applied to directly impede the function of driver oncogenes, thus far. Here, leveraging efforts from SOD model complexes, we report the novel finding of biomimetic copper complexes that efficiently scavenge intracellularly generated free radicals and, thereby, directly access the core consequence of colorectal cancer suppression. We conceived four structurally different SOD-mimicking copper complexes that showed distinct disproportionation reaction rates of intracellular superoxide radical anions. By replenishing SOD models, we observed a dramatic reduction of intracellular reactive oxygen species (ROS) and adenine 5′-triphosphate (ATP) concentrations that led to cell cycle arrest at the G2/M stage and induced apoptosis in vitro and in vivo. Our results showcase how nature-mimicking models can be designed and fine-tuned to serve as a viable chemotherapeutic strategy for cancer treatment.
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