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A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
Published on: February 21, 2025
Advances in nucleic acid therapeutics: structures, delivery systems, and future perspectives in cancer treatment
Leqi Zhang1, Wenting Lou1, Jianwei Wang2,3
1Department of Surgery, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Abstract:
Cancer has emerged as a significant threat to human health. Nucleic acid therapeutics regulate the gene expression process by introducing exogenous nucleic acid fragments, offering new possibilities for tumor remission and even cure. Their mechanism of action and high specificity demonstrate great potential in cancer treatment. However, nucleic acid drugs face challenges such as low stability and limited ability to cross physiological barriers in vivo. To address these issues, various nucleic acid delivery vectors have been developed to enhance the stability and facilitate precise targeted delivery of nucleic acid drugs within the body. In this review article, we primarily introduce the structures and principles of nucleic acid drugs commonly used in cancer therapy, as well as their cellular uptake and intracellular transportation processes. We focus on the various vectors commonly employed in nucleic acid drug delivery, highlighting their research progress and applications in recent years. Furthermore, we propose potential trends and prospects of nucleic acid drugs and their carriers in the future.
Insights
Nucleic acid therapeutics offer promising cancer treatment options by regulating gene expression. Delivery vectors are crucial for enhancing stability and targeted delivery of these novel cancer drugs.
Area of Science:
- Biomedical Engineering
- Molecular Biology
- Oncology
Background:
- Cancer remains a major global health challenge.
- Nucleic acid therapeutics represent a novel approach to cancer treatment by modulating gene expression.
- Challenges include poor stability and limited in vivo delivery of nucleic acid drugs.
Purpose of the Study:
- To review the structures and mechanisms of nucleic acid drugs for cancer therapy.
- To explore cellular uptake and intracellular transport of these therapeutics.
- To highlight advancements in nucleic acid delivery vectors for cancer treatment.
Main Methods:
- Literature review of nucleic acid drug structures and delivery systems.
- Analysis of cellular mechanisms involved in nucleic acid drug action.
- Evaluation of recent research progress and applications of delivery vectors.
Main Results:
- Nucleic acid drugs show high specificity and potential for tumor remission.
- Various delivery vectors have been developed to overcome stability and targeting limitations.
- Recent research demonstrates significant progress in vector design and application.
Conclusions:
- Nucleic acid therapeutics hold significant promise for cancer treatment.
- Effective delivery vectors are essential for realizing the full therapeutic potential.
- Future directions involve optimizing vectors for enhanced stability and targeted delivery.
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