Switching on prodrugs using radiotherapy.
Jin GengYichuan ZhangQuan GaoKevin NeumannHua DongHamish PorterMark A PotterHua RenDavid ArgyleMark BradleyPublished in: Nature chemistry (2021)
Chemotherapy is a powerful tool in the armoury against cancer, but it is fraught with problems due to its global systemic toxicity. Here we report the proof of concept of a chemistry-based strategy, whereby gamma/X-ray irradiation mediates the activation of a cancer prodrug, thereby enabling simultaneous chemo-radiotherapy with radiotherapy locally activating a prodrug. In an initial demonstration, we show the activation of a fluorescent probe using this approach. Expanding on this, we show how sulfonyl azide- and phenyl azide-caged prodrugs of pazopanib and doxorubicin can be liberated using clinically relevant doses of ionizing radiation. This strategy is different to conventional chemo-radiotherapy radiation, where chemo-sensitization of the cancer takes place so that subsequent radiotherapy is more effective. This approach could enable site-directed chemotherapy, rather than systemic chemotherapy, with 'real time' drug decaging at the tumour site. As such, it opens up a new era in targeted and directed chemotherapy.
Keyphrases
- locally advanced
- rectal cancer
- squamous cell carcinoma
- radiation therapy
- papillary thyroid
- cancer therapy
- early stage
- radiation induced
- fluorescent probe
- squamous cell
- signaling pathway
- drug delivery
- high resolution
- childhood cancer
- magnetic resonance
- drug induced
- mental health
- computed tomography
- young adults
- oxidative stress