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miRNA Pathway Alteration in Response to Non-Coding RNA Delivery in Viral Vector-Based Gene Therapy
Darya A Savenkova1, Aelita-Luiza A Makarova1, Igor K Shalik1
1State Research Center of Virology and Biotechnology "Vector," Federal Service for Surveillance on Consumer Rights Protection and Human Well-being (FBRI SRC VB "Vector", Rospotrebnadzor), Koltsovo 630559, Russia.
Gene therapy uses viral vectors to deliver genetic material but can cause immune responses and cytotoxicity. This review examines how viral vectors and non-coding RNA delivery impact miRNA pathways, crucial for gene regulation.
Area of Science:
- Biomedical Science
- Molecular Biology
- Gene Therapy
Background:
- Gene therapy, often using viral vectors, is a common treatment for incurable disorders.
- Viral vectors offer efficient cellular entry and genetic material delivery.
- However, viral vectors can trigger immune responses and cytotoxicity, potentially disrupting cellular metabolism and microRNA (miRNA) pathways.
Purpose of the Study:
- To review the impact of viral vector entry on miRNA signaling pathways.
- To evaluate the effects of non-coding RNA delivery via viral vectors on miRNA pathways.
- To highlight safety considerations in viral gene therapy related to miRNA pathway disruption.
Main Methods:
- Literature review of studies on viral vectors in gene therapy.
- Analysis of research on non-coding RNA delivery mechanisms.
- Examination of the interplay between viral components, non-coding RNAs, and cellular miRNA pathways.
Main Results:
- Viral vector components can directly or indirectly affect miRNA biogenesis and function.
- Delivered non-coding RNAs may interfere with endogenous miRNA targets and pathways.
- Disturbances in miRNA pathways can lead to unintended cellular consequences and toxicity.
Conclusions:
- Viral gene therapy necessitates careful evaluation of potential miRNA pathway disruptions.
- Understanding these interactions is crucial for improving the safety and efficacy of gene therapy.
- Further research is needed to mitigate adverse effects associated with viral vectors and non-coding RNA delivery.
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