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Protamine nanoparticles for improving shRNA-mediated anti-cancer effects
Protamine nanoparticles were designed by encapsulating small hairpin RNA (shRNA)-expressing plasmid DNA targeting the Bcl-2 gene (shBcl-2) to silence apoptosis-related Bcl-2 protein for improving the transfection efficiency and cytotoxicity in cancer therapy. Our findings demonstrated that the obtai...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385308/ https://www.ncbi.nlm.nih.gov/pubmed/25852425 http://dx.doi.org/10.1186/s11671-015-0845-z |
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author | Liu, Ming Feng, Bo Shi, Yijie Su, Chang Song, Huijuan Cheng, Wei Zhao, Liang |
author_facet | Liu, Ming Feng, Bo Shi, Yijie Su, Chang Song, Huijuan Cheng, Wei Zhao, Liang |
author_sort | Liu, Ming |
collection | PubMed |
description | Protamine nanoparticles were designed by encapsulating small hairpin RNA (shRNA)-expressing plasmid DNA targeting the Bcl-2 gene (shBcl-2) to silence apoptosis-related Bcl-2 protein for improving the transfection efficiency and cytotoxicity in cancer therapy. Our findings demonstrated that the obtained protamine nanoparticles possessed excellent characterizations of small particle size, homogenous distribution, positive charge, and high encapsulation efficiency of gene. shBcl-2 loaded in nanoparticles (NPs) was protected effectively from the degradation of DNase I and serum. More importantly, it significantly improved the efficiency of transfection of shRNA in vitro in A549 cells and increased its cytotoxicity and induced more cell apoptosis by silencing Bcl-2. |
format | Online Article Text |
id | pubmed-4385308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-43853082015-04-07 Protamine nanoparticles for improving shRNA-mediated anti-cancer effects Liu, Ming Feng, Bo Shi, Yijie Su, Chang Song, Huijuan Cheng, Wei Zhao, Liang Nanoscale Res Lett Nano Express Protamine nanoparticles were designed by encapsulating small hairpin RNA (shRNA)-expressing plasmid DNA targeting the Bcl-2 gene (shBcl-2) to silence apoptosis-related Bcl-2 protein for improving the transfection efficiency and cytotoxicity in cancer therapy. Our findings demonstrated that the obtained protamine nanoparticles possessed excellent characterizations of small particle size, homogenous distribution, positive charge, and high encapsulation efficiency of gene. shBcl-2 loaded in nanoparticles (NPs) was protected effectively from the degradation of DNase I and serum. More importantly, it significantly improved the efficiency of transfection of shRNA in vitro in A549 cells and increased its cytotoxicity and induced more cell apoptosis by silencing Bcl-2. Springer US 2015-03-19 /pmc/articles/PMC4385308/ /pubmed/25852425 http://dx.doi.org/10.1186/s11671-015-0845-z Text en © Liu et al. ; licensee Springer. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Nano Express Liu, Ming Feng, Bo Shi, Yijie Su, Chang Song, Huijuan Cheng, Wei Zhao, Liang Protamine nanoparticles for improving shRNA-mediated anti-cancer effects |
title | Protamine nanoparticles for improving shRNA-mediated anti-cancer effects |
title_full | Protamine nanoparticles for improving shRNA-mediated anti-cancer effects |
title_fullStr | Protamine nanoparticles for improving shRNA-mediated anti-cancer effects |
title_full_unstemmed | Protamine nanoparticles for improving shRNA-mediated anti-cancer effects |
title_short | Protamine nanoparticles for improving shRNA-mediated anti-cancer effects |
title_sort | protamine nanoparticles for improving shrna-mediated anti-cancer effects |
topic | Nano Express |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385308/ https://www.ncbi.nlm.nih.gov/pubmed/25852425 http://dx.doi.org/10.1186/s11671-015-0845-z |
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