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Published on: August 23, 2024
Combinatorial therapeutic approaches with RNAi and anticancer drugs using nanodrug delivery systems
Anish Babu1,2, Anupama Munshi2,3, Rajagopal Ramesh1,2,4
1a Department of Pathology , University of Oklahoma Health Sciences Center , Oklahoma City , OK , USA.
Abstract:
RNA interference (RNAi) is emerging as a powerful approach in cancer treatment. siRNA is an important RNAi tool that can be designed to specifically silence the expression of genes involved in drug resistance and chemotherapeutic inactivity. Combining siRNA and other therapeutic agents can overcome the multidrug resistance (MDR) phenomenon by simultaneously silencing genes and enhancing chemotherapeutic activity. Moreover, the therapeutic efficiency of anticancer drugs can be significantly improved by additive or synergistic effects induced by siRNA and combined therapies. Co-delivery of these diverse anticancer agents, however, requires specially designed nanocarriers. This review highlights the recent trends in siRNA/anticancer drug co-delivery systems under the major categories of liposomes/lipid, polymeric and inorganic nanoplatforms. The objective is to discuss the strategies for nanocarrier-based co-delivery systems using siRNA/anticancer drug combinations, emphasizing various siRNA targets that help overcome MDR and enhance therapeutic efficiency.
Insights
Small interfering RNA (siRNA) combined with chemotherapy offers a potent cancer treatment strategy. Nanocarriers are crucial for co-delivering siRNA and drugs to overcome multidrug resistance and enhance treatment efficacy.
Area of Science:
- Oncology
- Nanotechnology
- Molecular Biology
Background:
- RNA interference (RNAi) using small interfering RNA (siRNA) is a promising cancer therapy.
- siRNA can silence genes contributing to drug resistance and chemotherapeutic inactivity.
- Overcoming multidrug resistance (MDR) is critical for effective cancer treatment.
Purpose of the Study:
- To review recent advancements in co-delivery systems for siRNA and anticancer drugs.
- To discuss nanocarrier strategies for combining siRNA and chemotherapeutics.
- To highlight siRNA targets that enhance therapeutic efficiency and overcome MDR.
Main Methods:
- Review of current literature on nanoplatforms for siRNA/anticancer drug co-delivery.
- Categorization of nanocarriers into liposomal/lipid, polymeric, and inorganic systems.
- Analysis of strategies for enhancing therapeutic effects through combined delivery.
Main Results:
- Co-delivery systems using nanocarriers are essential for combining siRNA and anticancer drugs.
- Liposomal, polymeric, and inorganic nanoplatforms are key categories for these systems.
- Combined therapies demonstrate additive or synergistic effects, improving therapeutic outcomes.
Conclusions:
- Nanocarrier-mediated co-delivery of siRNA and anticancer drugs is a viable strategy to combat MDR.
- Optimizing siRNA targets and nanocarrier design can significantly improve cancer treatment efficacy.
- This approach holds potential for enhanced patient outcomes in oncology.
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