脱氢抗坏血酸
抗坏血酸
化学
肿瘤微环境
癌细胞
氧化还原
活性氧
细胞生物学
生物物理学
过氧化氢
生物化学
生物
癌症
癌症研究
肿瘤细胞
遗传学
食品科学
有机化学
作者
Zhongyuan Zeng,Jian Wang,Shuang Zhao,Yuchan Zhang,Jingchuan Fan,Hui Wu,Jiajia Chen,Zaikuan Zhang,Zexuan Meng,Yang Lu,Renzhi Wang,Bo Zhang,Guixue Wang,Chenzhong Li,Guangchao Zang
标识
DOI:10.1002/advs.202304079
摘要
Abstract Malignant tumors pose a serious risk to human health. Ascorbic acid (AA) has potential for tumor therapy; however, the mechanism underlying the ability of AA to selectively kill tumor cells remains unclear. AA can cause redox disequilibrium in tumor cells, resulting in the release of abundant reactive oxygen species, represented by hydrogen peroxide (H 2 O 2 ). Therefore, the detection of H 2 O 2 changes can provide insight into the selective killing mechanism of AA against tumor cells. In this work, inspired by the ion‐exchange mechanism in coral formation, a flexible H 2 O 2 sensor (PtNFs/CoPi@CC) is constructed to monitor the dynamics of H 2 O 2 in the cell microenvironment, which exhibits excellent sensitivity and spatiotemporal resolution. Moreover, the findings suggest that dehydroascorbic acid (DHA), the oxidation product of AA, is highly possible the substance that actually acts on tumor cells in AA therapy. Additionally, the intracellular redox disequilibrium and H 2 O 2 release caused by DHA are positively correlated with the abundance and activity of glucose transporter 1 (GLUT1). In conclusion, this work has revealed the potential mechanism underlying the ability of AA to selectively kill tumor cells through the construction and use of PtNFs/CoPi@CC. The findings provide new insights into the clinical application of AA.
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