Cargando…

Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy

Cancer stem cell-like cells (CSCL) are responsible for tumor recurrence associated with conventional therapy (e.g. surgery, radiation, and chemotherapy). Here, we developed a novel multifunctional nucleus-targeting nanoparticle-based gene delivery system which is capable of targeting and eradicating...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Ling, Li, Xia, Wu, Yuzhe, Song, Linjiang, Yang, Xi, He, Tao, Wang, Ning, Yang, Suleixin, Zeng, Yan, Wu, Qinjie, Qian, Zhiyong, Wei, Yuquan, Gong, Changyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436517/
https://www.ncbi.nlm.nih.gov/pubmed/28529641
http://dx.doi.org/10.7150/thno.17588
_version_ 1783237421777813504
author Li, Ling
Li, Xia
Wu, Yuzhe
Song, Linjiang
Yang, Xi
He, Tao
Wang, Ning
Yang, Suleixin
Zeng, Yan
Wu, Qinjie
Qian, Zhiyong
Wei, Yuquan
Gong, Changyang
author_facet Li, Ling
Li, Xia
Wu, Yuzhe
Song, Linjiang
Yang, Xi
He, Tao
Wang, Ning
Yang, Suleixin
Zeng, Yan
Wu, Qinjie
Qian, Zhiyong
Wei, Yuquan
Gong, Changyang
author_sort Li, Ling
collection PubMed
description Cancer stem cell-like cells (CSCL) are responsible for tumor recurrence associated with conventional therapy (e.g. surgery, radiation, and chemotherapy). Here, we developed a novel multifunctional nucleus-targeting nanoparticle-based gene delivery system which is capable of targeting and eradicating CSCL. These nanoparticles can facilitate efficient endosomal escape and spontaneously penetrate into nucleus without additional nuclear localization signal. They also induced extremely high gene transfection efficiency (>95%) even in culture medium containing 30% serum, which significantly surpassed that of some commercial transfection reagents, such as Lipofectamine 2000 and Lipofectamine 3000 etc. Especially, when loaded with the TRAIL gene, this system mediated remarkable depletion of CSCL. Upon systemic administration, the nanoparticles accumulated in tumor sites while sparing the non-cancer tissues and significantly inhibited the growth of tumors with no evident systemic toxicity. Taken together, our results suggest that these novel multifunctional, nucleus-targeting nanoparticles are a very promising in vivo gene delivery system capable of targeting CSCL and represent a new treatment candidate for improving the survival of cancer patients.
format Online
Article
Text
id pubmed-5436517
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-54365172017-05-19 Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy Li, Ling Li, Xia Wu, Yuzhe Song, Linjiang Yang, Xi He, Tao Wang, Ning Yang, Suleixin Zeng, Yan Wu, Qinjie Qian, Zhiyong Wei, Yuquan Gong, Changyang Theranostics Research Paper Cancer stem cell-like cells (CSCL) are responsible for tumor recurrence associated with conventional therapy (e.g. surgery, radiation, and chemotherapy). Here, we developed a novel multifunctional nucleus-targeting nanoparticle-based gene delivery system which is capable of targeting and eradicating CSCL. These nanoparticles can facilitate efficient endosomal escape and spontaneously penetrate into nucleus without additional nuclear localization signal. They also induced extremely high gene transfection efficiency (>95%) even in culture medium containing 30% serum, which significantly surpassed that of some commercial transfection reagents, such as Lipofectamine 2000 and Lipofectamine 3000 etc. Especially, when loaded with the TRAIL gene, this system mediated remarkable depletion of CSCL. Upon systemic administration, the nanoparticles accumulated in tumor sites while sparing the non-cancer tissues and significantly inhibited the growth of tumors with no evident systemic toxicity. Taken together, our results suggest that these novel multifunctional, nucleus-targeting nanoparticles are a very promising in vivo gene delivery system capable of targeting CSCL and represent a new treatment candidate for improving the survival of cancer patients. Ivyspring International Publisher 2017-04-10 /pmc/articles/PMC5436517/ /pubmed/28529641 http://dx.doi.org/10.7150/thno.17588 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Li, Ling
Li, Xia
Wu, Yuzhe
Song, Linjiang
Yang, Xi
He, Tao
Wang, Ning
Yang, Suleixin
Zeng, Yan
Wu, Qinjie
Qian, Zhiyong
Wei, Yuquan
Gong, Changyang
Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy
title Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy
title_full Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy
title_fullStr Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy
title_full_unstemmed Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy
title_short Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene Therapy
title_sort multifunctional nucleus-targeting nanoparticles with ultra-high gene transfection efficiency for in vivo gene therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436517/
https://www.ncbi.nlm.nih.gov/pubmed/28529641
http://dx.doi.org/10.7150/thno.17588
work_keys_str_mv AT liling multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT lixia multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT wuyuzhe multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT songlinjiang multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT yangxi multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT hetao multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT wangning multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT yangsuleixin multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT zengyan multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT wuqinjie multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT qianzhiyong multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT weiyuquan multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy
AT gongchangyang multifunctionalnucleustargetingnanoparticleswithultrahighgenetransfectionefficiencyforinvivogenetherapy