An Activatable Photosensitizer Targeting Human NAD(P)H: Quinone Oxidoreductase 1.
Elyse M DigbyOleg SadovskiAndrew A BeharryPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
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.
Keyphrases
- photodynamic therapy
- electron transfer
- endothelial cells
- fluorescence imaging
- papillary thyroid
- squamous cell
- living cells
- quantum dots
- induced pluripotent stem cells
- fluorescent probe
- high resolution
- magnetic resonance
- gene expression
- small molecule
- computed tomography
- squamous cell carcinoma
- magnetic resonance imaging
- drug delivery
- young adults
- high speed
- cancer therapy