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Generation of Cationic Nanoliposomes for the Efficient Delivery of In Vitro Transcribed Messenger RNA
Published on: February 1, 2019
Targeted Liposomes: A Nonviral Gene Delivery System for Cancer Therapy
Marcela Tavares Luiz1, Jessyca Aparecida Paes Dutra2, Larissa Bueno Tofani2
1School of Pharmaceutical Science of Ribeirao Preto, University of Sao Paulo (USP), Ribeirao Preto 14040-900, Brazil.
Abstract:
Cancer is the second most frequent cause of death worldwide, with 28.4 million new cases expected for 2040. Despite de advances in the treatment, it remains a challenge because of the tumor heterogenicity and the increase in multidrug resistance mechanisms. Thus, gene therapy has been a potential therapeutic approach owing to its ability to introduce, silence, or change the content of the human genetic code for inhibiting tumor progression, angiogenesis, and metastasis. For the proper delivery of genes to tumor cells, it requires the use of gene vectors for protecting the therapeutic gene and transporting it into cells. Among these vectors, liposomes have been the nonviral vector most used because of their low immunogenicity and low toxicity. Furthermore, this nanosystem can have its surface modified with ligands (e.g., antibodies, peptides, aptamers, folic acid, carbohydrates, and others) that can be recognized with high specificity and affinity by receptor overexpressed in tumor cells, increasing the selective delivery of genes to tumors. In this context, the present review address and discuss the main targeting ligands used to functionalize liposomes for improving gene delivery with potential application in cancer treatment.
Insights
Gene therapy offers a promising cancer treatment approach. Functionalized liposomes enhance targeted gene delivery to tumor cells, improving treatment efficacy and reducing side effects.
Area of Science:
- Oncology
- Biotechnology
- Nanomedicine
Background:
- Cancer is a leading global cause of death, with increasing incidence and challenges from tumor heterogeneity and multidrug resistance.
- Gene therapy presents a potential therapeutic strategy by modifying the genetic code to inhibit tumor progression, angiogenesis, and metastasis.
- Effective gene delivery to tumor cells requires specialized vectors to protect and transport therapeutic genes.
Purpose of the Study:
- To review and discuss targeting ligands used for functionalizing liposomes.
- To explore the potential of ligand-functionalized liposomes in improving gene delivery for cancer treatment.
Main Methods:
- Review of scientific literature on gene therapy, liposomes, and targeting ligands for cancer treatment.
- Analysis of different types of targeting ligands (antibodies, peptides, aptamers, folic acid, carbohydrates) used in liposome functionalization.
- Discussion of the role of receptor-ligand interactions in selective tumor targeting.
Main Results:
- Liposomes are effective nonviral vectors for gene delivery due to low immunogenicity and toxicity.
- Surface modification of liposomes with specific ligands enhances selective gene delivery to tumor cells overexpressing target receptors.
- Targeting ligands facilitate high-affinity binding to tumor cells, improving the efficiency of gene therapy.
Conclusions:
- Ligand-functionalized liposomes represent a significant advancement in targeted gene delivery for cancer therapy.
- Optimizing ligand selection and liposome design can further enhance the efficacy and specificity of gene-based cancer treatments.
- This approach holds considerable promise for developing novel and more effective cancer treatment strategies.
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