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A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics
The highly efficient cancer cell targeted delivery plays an important role in precise targeted therapies. Herein, a multifunctional DNA nano-scorpion nanostructure (termed AptDzy-DNS) functioned with aptamers and DNAzyme is developed for highly efficient targeted delivery of mRNA therapeutics in gen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033943/ https://www.ncbi.nlm.nih.gov/pubmed/29976947 http://dx.doi.org/10.1038/s41598-018-28542-3 |
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author | Li, Dandan Mo, Fei Wu, Jiangling Huang, Yong Zhou, Huihao Ding, Shijia Chen, Weixian |
author_facet | Li, Dandan Mo, Fei Wu, Jiangling Huang, Yong Zhou, Huihao Ding, Shijia Chen, Weixian |
author_sort | Li, Dandan |
collection | PubMed |
description | The highly efficient cancer cell targeted delivery plays an important role in precise targeted therapies. Herein, a multifunctional DNA nano-scorpion nanostructure (termed AptDzy-DNS) functioned with aptamers and DNAzyme is developed for highly efficient targeted delivery of mRNA therapeutics in gene therapy. The designed AptDzy-DNS is self-assembled with specific aptamers as “scorpion stingers” for targeting tumor cell and DNAzymes as “scorpion pincers” for targeted gene therapy by cleaving mRNA into fragments. The as-prepared AptDzy-DNS can effectively distinguish cancer cells from normal cells by specific cross-talking between aptamers on AptDzy-DNS and overexpressed cell-surface receptors. In the process of gene therapy, by reacting with Mg(2+)-dependent DNAzyme on AptDzy-DNS, the mRNA oligonucleotide in cancer cell is auto-cleaved into broken strand, failing to be translated into corresponding protein. Following, the downregulation protein can block cancer cell growth and realize highly efficient targeted therapies. The results demonstrate that the multifunctional AptDzy-DNS shows promise for targeted cancer cell discrimination, highly efficient targeted delivery of mRNA therapeutics in gene therapy. Thus, this developed strategy provides impressive improvement on gene targeted therapy and paves the way for application of AptDzy-DNS in human cancer targeted therapies. |
format | Online Article Text |
id | pubmed-6033943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60339432018-07-12 A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics Li, Dandan Mo, Fei Wu, Jiangling Huang, Yong Zhou, Huihao Ding, Shijia Chen, Weixian Sci Rep Article The highly efficient cancer cell targeted delivery plays an important role in precise targeted therapies. Herein, a multifunctional DNA nano-scorpion nanostructure (termed AptDzy-DNS) functioned with aptamers and DNAzyme is developed for highly efficient targeted delivery of mRNA therapeutics in gene therapy. The designed AptDzy-DNS is self-assembled with specific aptamers as “scorpion stingers” for targeting tumor cell and DNAzymes as “scorpion pincers” for targeted gene therapy by cleaving mRNA into fragments. The as-prepared AptDzy-DNS can effectively distinguish cancer cells from normal cells by specific cross-talking between aptamers on AptDzy-DNS and overexpressed cell-surface receptors. In the process of gene therapy, by reacting with Mg(2+)-dependent DNAzyme on AptDzy-DNS, the mRNA oligonucleotide in cancer cell is auto-cleaved into broken strand, failing to be translated into corresponding protein. Following, the downregulation protein can block cancer cell growth and realize highly efficient targeted therapies. The results demonstrate that the multifunctional AptDzy-DNS shows promise for targeted cancer cell discrimination, highly efficient targeted delivery of mRNA therapeutics in gene therapy. Thus, this developed strategy provides impressive improvement on gene targeted therapy and paves the way for application of AptDzy-DNS in human cancer targeted therapies. Nature Publishing Group UK 2018-07-05 /pmc/articles/PMC6033943/ /pubmed/29976947 http://dx.doi.org/10.1038/s41598-018-28542-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Dandan Mo, Fei Wu, Jiangling Huang, Yong Zhou, Huihao Ding, Shijia Chen, Weixian A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics |
title | A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics |
title_full | A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics |
title_fullStr | A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics |
title_full_unstemmed | A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics |
title_short | A multifunctional DNA nano-scorpion for highly efficient targeted delivery of mRNA therapeutics |
title_sort | multifunctional dna nano-scorpion for highly efficient targeted delivery of mrna therapeutics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033943/ https://www.ncbi.nlm.nih.gov/pubmed/29976947 http://dx.doi.org/10.1038/s41598-018-28542-3 |
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