心脏毒性
过氧亚硝酸盐
化学
蒽环类
生物标志物
药理学
过氧亚硝酸
癌症研究
内科学
癌症
毒性
生物化学
医学
乳腺癌
酶
有机化学
超氧化物
作者
Xilei Xie,Fuyan Tang,Guangzhao Liu,Yong Li,Xingxing Su,Xiaoyun Jiao,Xu Wang,Bo Tang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2018-09-10
卷期号:90 (19): 11629-11635
被引量:104
标识
DOI:10.1021/acs.analchem.8b03207
摘要
Anthracyclines rank among the most efficacious anticancer medications. However, their clinical utility and oncologic efficacy are severely compromised by the cardiotoxicity risk facing the early-diagnosis difficulty and their unclear molecular mechanism. Herein, a two-photon-excitable and near-infrared-emissive fluorescent probe, TPNIR-FP, was fabricated and endowed with extraordinary specificity and sensitivity and a rapid response toward peroxynitrite (ONOO–), as well as mitochondria-targeting ability. With the aid of TPNIR-FP, we demonstrate that mitochondrial ONOO– is upregulated in the early stage and contributes to the onset and progression of anthracycline cardiotoxicity in cardiomyocyte and mouse models; therefore, it represents an early biomarker to predict subclinical cardiotoxicity induced by drug challenge. Furthermore, TPNIR-FP is proved to be a robust imaging tool to provide critical insights into drug-induced cardiotoxicity and other ONOO–-related pathophysiological processes.
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