
Nucleic acid degradation as barrier to gene delivery : a guide to understand and overcome nuclease activity
- Author
- Heyang Zhang, Jo Vandesompele (UGent) , Kevin Braeckmans (UGent) , Stefaan De Smedt (UGent) and Katrien Remaut (UGent)
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- Abstract
- Gene therapy is on its way to revolutionize the treatment of both inherited and acquired diseases, by transferring nucleic acids to correct a disease-causing gene in the target cells of patients. In the fight against infectious diseases, mRNA-based therapeutics have proven to be a viable strategy in the recent Covid-19 pandemic. Although a growing number of gene therapies have been approved, the success rate is limited when compared to the large number of preclinical and clinical trials that have been/are being performed. In this review, we highlight some of the hurdles which gene therapies encounter after administration into the human body, with a focus on nucleic acid degradation by nucleases that are extremely abundant in mammalian organs, biological fluids as well as in subcellular compartments. We overview the available strategies to reduce the biodegradation of gene therapeutics after administration, including chemical modifications of the nucleic acids, encapsulation into vectors and co-administration with nuclease inhibitors and discuss which strategies are applied for clinically approved nucleic acid therapeutics. In the final part, we discuss the currently available methods and techniques to qualify and quantify the integrity of nucleic acids, with their own strengths and limitations. This review discusses DNases and RNases present in the human body, strategies to reduce the degradation of gene therapeutics after administration and available methods to follow nuclease activity in buffer and living cells.
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01HQ8GNXRE5JXTAKYMWVWAN6RM
- MLA
- Zhang, Heyang, et al. “Nucleic Acid Degradation as Barrier to Gene Delivery : A Guide to Understand and Overcome Nuclease Activity.” CHEMICAL SOCIETY REVIEWS, vol. 53, no. 1, 2024, pp. 317–60, doi:10.1039/d3cs00194f.
- APA
- Zhang, H., Vandesompele, J., Braeckmans, K., De Smedt, S., & Remaut, K. (2024). Nucleic acid degradation as barrier to gene delivery : a guide to understand and overcome nuclease activity. CHEMICAL SOCIETY REVIEWS, 53(1), 317–360. https://doi.org/10.1039/d3cs00194f
- Chicago author-date
- Zhang, Heyang, Jo Vandesompele, Kevin Braeckmans, Stefaan De Smedt, and Katrien Remaut. 2024. “Nucleic Acid Degradation as Barrier to Gene Delivery : A Guide to Understand and Overcome Nuclease Activity.” CHEMICAL SOCIETY REVIEWS 53 (1): 317–60. https://doi.org/10.1039/d3cs00194f.
- Chicago author-date (all authors)
- Zhang, Heyang, Jo Vandesompele, Kevin Braeckmans, Stefaan De Smedt, and Katrien Remaut. 2024. “Nucleic Acid Degradation as Barrier to Gene Delivery : A Guide to Understand and Overcome Nuclease Activity.” CHEMICAL SOCIETY REVIEWS 53 (1): 317–360. doi:10.1039/d3cs00194f.
- Vancouver
- 1.Zhang H, Vandesompele J, Braeckmans K, De Smedt S, Remaut K. Nucleic acid degradation as barrier to gene delivery : a guide to understand and overcome nuclease activity. CHEMICAL SOCIETY REVIEWS. 2024;53(1):317–60.
- IEEE
- [1]H. Zhang, J. Vandesompele, K. Braeckmans, S. De Smedt, and K. Remaut, “Nucleic acid degradation as barrier to gene delivery : a guide to understand and overcome nuclease activity,” CHEMICAL SOCIETY REVIEWS, vol. 53, no. 1, pp. 317–360, 2024.
@article{01HQ8GNXRE5JXTAKYMWVWAN6RM, abstract = {{Gene therapy is on its way to revolutionize the treatment of both inherited and acquired diseases, by transferring nucleic acids to correct a disease-causing gene in the target cells of patients. In the fight against infectious diseases, mRNA-based therapeutics have proven to be a viable strategy in the recent Covid-19 pandemic. Although a growing number of gene therapies have been approved, the success rate is limited when compared to the large number of preclinical and clinical trials that have been/are being performed. In this review, we highlight some of the hurdles which gene therapies encounter after administration into the human body, with a focus on nucleic acid degradation by nucleases that are extremely abundant in mammalian organs, biological fluids as well as in subcellular compartments. We overview the available strategies to reduce the biodegradation of gene therapeutics after administration, including chemical modifications of the nucleic acids, encapsulation into vectors and co-administration with nuclease inhibitors and discuss which strategies are applied for clinically approved nucleic acid therapeutics. In the final part, we discuss the currently available methods and techniques to qualify and quantify the integrity of nucleic acids, with their own strengths and limitations. This review discusses DNases and RNases present in the human body, strategies to reduce the degradation of gene therapeutics after administration and available methods to follow nuclease activity in buffer and living cells.}}, author = {{Zhang, Heyang and Vandesompele, Jo and Braeckmans, Kevin and De Smedt, Stefaan and Remaut, Katrien}}, issn = {{0306-0012}}, journal = {{CHEMICAL SOCIETY REVIEWS}}, language = {{eng}}, number = {{1}}, pages = {{317--360}}, title = {{Nucleic acid degradation as barrier to gene delivery : a guide to understand and overcome nuclease activity}}, url = {{http://doi.org/10.1039/d3cs00194f}}, volume = {{53}}, year = {{2024}}, }
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