An Activatable Photosensitizer Targeting Human NAD(P)H: Quinone Oxidoreductase 1

被引:31
|
作者
Digby, Elyse M. [1 ]
Sadovski, Oleg [1 ]
Beharry, Andrew A. [1 ]
机构
[1] Univ Toronto, Dept Chem & Phys Sci, 3359 Mississauga Rd North, Mississauga, ON L5L 1C6, Canada
关键词
cancer; hNQO1; phenalenones; photosensitizers; reactive oxygen species; BIOLOGICAL EVALUATION; FLUORESCENT-PROBE; DT-DIAPHORASE; CANCER-CELLS; TURN-ON; NQO1; HYPOXIA; DESIGN; VISUALIZATION; PHENALENONE;
D O I
10.1002/chem.201904607
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Human NAD(P)H: Quinone Oxidoreductase 1 (hNQO1) is an attractive enzyme for cancer therapeutics due to its significant overexpression in tumors compared to healthy tissues. Its unique catalytic mechanism involving the two-electron reduction of quinone-based compounds has made it a useful target to exploit in the design of hNQO1 fluorescent chemosensors and hNQO1-activatable-prodrugs. In this work, hNQO1 is exploited for an optical therapeutic. The probe uses the photosensitizer, phenalenone, which is initially quenched via photo-induced electron transfer by the attached quinone. Native phenalenone is liberated in the presence of hNQO1 resulting in the production of cytotoxic singlet oxygen upon irradiation. hNQO1-mediated activation in A549 lung cancer cells containing high levels of hNQO1 induces a dose-dependent photo-cytotoxic response after irradiation. In contrast, no photo-cytotoxicity was observed in the normal lung cell line, MRC9. By targeting hNQO1, this scaffold can be used to enhance the cancer selectivity of photodynamic therapy.
引用
收藏
页码:2713 / 2718
页数:6
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