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pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment

RNA interference (RNAi) is a biological process through which gene expression can be inhibited by RNA molecules with high selectivity and specificity, providing a promising tool for tumor treatment. Two types of molecules are often applied to inactivate target gene expression: synthetic double stran...

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Autores principales: Li, Xiaoming, Guo, Xiaoshuang, Cheng, Yuan, Zhao, Xiaotian, Fang, Zhiwei, Luo, Yanli, Xia, Shujun, Feng, Yun, Chen, Jianjun, Yuan, Wei-En
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167493/
https://www.ncbi.nlm.nih.gov/pubmed/30319959
http://dx.doi.org/10.3389/fonc.2018.00354
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author Li, Xiaoming
Guo, Xiaoshuang
Cheng, Yuan
Zhao, Xiaotian
Fang, Zhiwei
Luo, Yanli
Xia, Shujun
Feng, Yun
Chen, Jianjun
Yuan, Wei-En
author_facet Li, Xiaoming
Guo, Xiaoshuang
Cheng, Yuan
Zhao, Xiaotian
Fang, Zhiwei
Luo, Yanli
Xia, Shujun
Feng, Yun
Chen, Jianjun
Yuan, Wei-En
author_sort Li, Xiaoming
collection PubMed
description RNA interference (RNAi) is a biological process through which gene expression can be inhibited by RNA molecules with high selectivity and specificity, providing a promising tool for tumor treatment. Two types of molecules are often applied to inactivate target gene expression: synthetic double stranded small interfering RNA (siRNA) and plasmid DNA encoding short hairpin RNA (shRNA). Vectors with high transfection efficiency and low toxicity are essential for the delivery of siRNA and shRNA. In this study, TDAPEI, the synthetic derivative of low-molecular-weight polyethylenimine (PEI), was cross-linked with imine bonds by the conjugation of branched PEI (1.8 kDa) and 2,5-thiophenedicarboxaldehyde (TDA). This biodegradable cationic polymer was utilized as the vector for the delivery of plasmid DNA expressing anti-VEGF-shRNA. Compared to PEI (25 kDa), TDAPEI had a better performance since experimental results suggest its higher transfection efficiency as well as lower toxicity both in cell and animal studies. TDAPEI did not stimulate innate immune response, which is a significant factor that should be considered in vector design for gene delivery. All the results suggested that TDAPEI delivering anti-VEGF-shRNA may provide a promising method for tumor treatment.
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spelling pubmed-61674932018-10-12 pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment Li, Xiaoming Guo, Xiaoshuang Cheng, Yuan Zhao, Xiaotian Fang, Zhiwei Luo, Yanli Xia, Shujun Feng, Yun Chen, Jianjun Yuan, Wei-En Front Oncol Oncology RNA interference (RNAi) is a biological process through which gene expression can be inhibited by RNA molecules with high selectivity and specificity, providing a promising tool for tumor treatment. Two types of molecules are often applied to inactivate target gene expression: synthetic double stranded small interfering RNA (siRNA) and plasmid DNA encoding short hairpin RNA (shRNA). Vectors with high transfection efficiency and low toxicity are essential for the delivery of siRNA and shRNA. In this study, TDAPEI, the synthetic derivative of low-molecular-weight polyethylenimine (PEI), was cross-linked with imine bonds by the conjugation of branched PEI (1.8 kDa) and 2,5-thiophenedicarboxaldehyde (TDA). This biodegradable cationic polymer was utilized as the vector for the delivery of plasmid DNA expressing anti-VEGF-shRNA. Compared to PEI (25 kDa), TDAPEI had a better performance since experimental results suggest its higher transfection efficiency as well as lower toxicity both in cell and animal studies. TDAPEI did not stimulate innate immune response, which is a significant factor that should be considered in vector design for gene delivery. All the results suggested that TDAPEI delivering anti-VEGF-shRNA may provide a promising method for tumor treatment. Frontiers Media S.A. 2018-09-25 /pmc/articles/PMC6167493/ /pubmed/30319959 http://dx.doi.org/10.3389/fonc.2018.00354 Text en Copyright © 2018 Li, Guo, Cheng, Zhao, Fang, Luo, Xia, Feng, Chen and Yuan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Li, Xiaoming
Guo, Xiaoshuang
Cheng, Yuan
Zhao, Xiaotian
Fang, Zhiwei
Luo, Yanli
Xia, Shujun
Feng, Yun
Chen, Jianjun
Yuan, Wei-En
pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment
title pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment
title_full pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment
title_fullStr pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment
title_full_unstemmed pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment
title_short pH-Responsive Cross-Linked Low Molecular Weight Polyethylenimine as an Efficient Gene Vector for Delivery of Plasmid DNA Encoding Anti-VEGF-shRNA for Tumor Treatment
title_sort ph-responsive cross-linked low molecular weight polyethylenimine as an efficient gene vector for delivery of plasmid dna encoding anti-vegf-shrna for tumor treatment
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167493/
https://www.ncbi.nlm.nih.gov/pubmed/30319959
http://dx.doi.org/10.3389/fonc.2018.00354
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