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Imaging Tumorous Methylglyoxal by an Activatable Near-Infrared Fluorescent Probe for Monitoring Glyoxalase 1 Activity
被引:29
|作者:
Ding, Chunyong
[2
]
Wang, Fengyang
[1
]
Dang, Yijing
[1
]
Xu, Zhiai
[1
]
Li, Lingling
[1
]
Lai, Yi
[1
]
Yu, Haijun
[3
]
Luo, Yi
[4
]
Huang, Ruimin
[3
]
Zhang, Ao
[2
]
Zhang, Wen
[1
]
机构:
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200241, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[4] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
基金:
中国国家自然科学基金;
关键词:
ALZHEIMERS-DISEASE;
I INHIBITION;
APOPTOSIS;
PLASMA;
3-DEOXYGLUCOSONE;
MECHANISM;
GLYCATION;
OBESITY;
STRESS;
CELLS;
D O I:
10.1021/acs.analchem.9b03600
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
The accurate detection of tumorous methylglyoxal (MGO) and its detoxifier glyoxalase 1 (GLO1) in living systems is critical for understanding their roles in tumor initiation and progression. To date, the in situ fluorescence detection of endogenous MGO and GLO1 in tumor has not been reported. Herein we developed a near-infrared (NIR) fluorescent probe MEBTD to specifically detect tumorous MGO. Compared with previously reported MGO fluorescent probes, MEBTD exhibits several distinct advantages, including NIR emission, high selectivity with an MGO detection limit of 18 nM, and a 131-fold off-on ratio. The probe could sense GLO1 activity and monitor the therapeutic effect of GLO1 inhibitors by imaging tumorous MGO in a both a real-time and in situ manner, demonstrating that the biological effect of GLO1 inhibitors is dependent on the GLO1 activity. Furthermore, MEBTD enables the visualization of tumorous MGO induced by GLO1 inhibitors in vivo. To the best of our knowledge, MEBTD is the first NIR fluorescent probe for specifically imaging tumorous MGO in living animals, indicating the promising potential for tumor diagnosis and therapeutic evaluation.
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页码:15577 / 15584
页数:8
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