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Smart nanocarriers for enzyme-activated prodrug therapy
Louay Abo Qoura1,2, Elena Morozova3, С S Ramaa4
1Research Institute of Molecular and Cellular Medicine, People's Friendship University of Russia (RUDN University), Moscow, Russia.
Journal of Drug Targeting
|July 24, 2024
Summary
Enzyme-activated prodrug therapy (EPT) uses enzymes to convert non-toxic prodrugs into cancer-killing drugs at targeted sites. This review explores EPT
Area of Science:
- Biochemistry
- Oncology
- Nanotechnology
Background:
- Exogenous enzyme-activated prodrug therapy (EPT) is a targeted cancer treatment strategy.
- It involves delivering non-human enzymes to convert prodrugs into active cytotoxic agents.
- EPT has been researched for over 30 years with several agents progressing to clinical trials.
Purpose of the Study:
- To review the potential of EPT as a promising anticancer treatment.
- To list microbial, plant, and viral enzyme-prodrug systems that have reached clinical trials.
- To discuss emerging trends in EPT nanocarriers and nanotechnology applications.
Main Methods:
- Literature review of enzyme-activated prodrug therapy research.
- Identification of enzyme-prodrug pairs that have advanced to clinical trials.
- Analysis of novel nanocarrier systems for EPT, including nanobubbles, PICsomes, nanoparticles, and EVs.
Main Results:
- Several EPT pharmacological pairs have been developed and tested in clinical trials.
- A few EPT strategies have been successfully applied in specific cancer therapies.
- New nanocarrier technologies enhance EPT efficacy through targeted delivery and stimuli-triggered release.
Conclusions:
- EPT represents a significant advancement in targeted cancer therapy.
- Nanotechnology, particularly nanocarriers, offers innovative approaches to improve EPT efficacy and specificity.
- Continued research in EPT and nanocarrier systems holds great promise for future cancer treatment strategies.

