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Cell-Based Nanoparticles Delivery Systems for Targeted Cancer Therapy: Lessons from Anti-Angiogenesis Treatments
Paz de la Torre1, María Jesús Pérez-Lorenzo1, Álvaro Alcázar-Garrido1
1Grupo de Medicina Regenerativa, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Avda, 28041 Cordoba s/n, Madrid, Spain.
Abstract:
The main strategy of cancer treatment has focused on attacking the tumor cells. Some cancers initially responsive to chemotherapy become treatment-resistant. Another strategy is to block the formation of tumor vessels. However, tumors also become resistant to anti-angiogenic treatments, mostly due to other cells and factors present in the tumor microenvironment, and hypoxia in the central part of the tumor. The need for new cancer therapies is significant. The use of nanoparticle-based therapy will improve therapeutic efficacy and targeting, while reducing toxicity. However, due to inefficient accumulation in tumor sites, clearance by reticuloendothelial organs and toxicity, internalization or conjugation of drug-loaded nanoparticles (NPs) into mesenchymal stem cells (MSCs) can increase efficacy by actively delivering them into the tumor microenvironment. Nanoengineering MSCs with drug-loaded NPs can increase the drug payload delivered to tumor sites due to the migratory and homing abilities of MSCs. However, MSCs have some disadvantages, and exosomes and membranes from different cell types can be used to transport drug-loaded NPs actively to tumors. This review gives an overview of different cancer approaches, with a focus on hypoxia and the emergence of NPs as drug-delivery systems and MSCs as cellular vehicles for targeted delivery due to their tumor-homing potential.
Insights
New cancer therapies leverage nanoparticle (NP)-loaded mesenchymal stem cells (MSCs) for targeted drug delivery. This approach enhances therapeutic efficacy by utilizing MSCs
Area of Science:
- Oncology
- Nanotechnology
- Biomedical Engineering
Background:
- Conventional cancer treatments like chemotherapy and anti-angiogenic therapies face challenges with tumor resistance.
- Tumor resistance is often driven by the tumor microenvironment, including hypoxia and cellular factors.
- There is a significant need for novel therapeutic strategies to overcome cancer treatment resistance.
Purpose of the Study:
- To review current cancer treatment strategies, focusing on hypoxia and emerging drug delivery systems.
- To explore the potential of nanoparticle (NP)-based therapies for improved cancer treatment.
- To discuss the use of mesenchymal stem cells (MSCs) as cellular vehicles for targeted NP delivery.
Main Methods:
- Review of existing literature on cancer therapies, nanoparticle drug delivery, and stem cell applications.
- Analysis of the role of the tumor microenvironment, particularly hypoxia, in treatment resistance.
- Examination of strategies for enhancing NP delivery using cellular carriers like MSCs, exosomes, and cell membranes.
Main Results:
- Nanoparticle-based therapies offer improved efficacy and targeting while reducing toxicity compared to conventional methods.
- Internalizing or conjugating drug-loaded NPs into MSCs enhances drug accumulation at tumor sites.
- Exosomes and cell membranes can also serve as effective carriers for drug-loaded NPs, overcoming MSC limitations.
Conclusions:
- Nanoengineering MSCs with drug-loaded NPs presents a promising strategy for targeted cancer therapy.
- The inherent migratory and homing abilities of MSCs facilitate efficient drug delivery to tumors.
- Alternative carriers like exosomes and cell membranes offer further potential for optimizing NP-based cancer treatments.
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