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Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis
Cell-penetrating peptide (CPP) based delivery have provided immense potential for the therapeutic applications, however, most of nonhuman originated CPPs carry the risk of possible cytotoxicity and immunogenicity, thus may restricting to be used. Here, we describe a novel human-derived CPP, denoted...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226491/ https://www.ncbi.nlm.nih.gov/pubmed/27081693 http://dx.doi.org/10.18632/oncotarget.8682 |
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author | Wang, Hu Ma, Jie-Lan Yang, Ying-Gui Song, Yang Wu, Jiao Qin, Yan-Yan Zhao, Xue-Li Wang, Jun Zou, Li-Li Wu, Jiang-Feng Li, Jun-Ming Liu, Chang-Bai |
author_facet | Wang, Hu Ma, Jie-Lan Yang, Ying-Gui Song, Yang Wu, Jiao Qin, Yan-Yan Zhao, Xue-Li Wang, Jun Zou, Li-Li Wu, Jiang-Feng Li, Jun-Ming Liu, Chang-Bai |
author_sort | Wang, Hu |
collection | PubMed |
description | Cell-penetrating peptide (CPP) based delivery have provided immense potential for the therapeutic applications, however, most of nonhuman originated CPPs carry the risk of possible cytotoxicity and immunogenicity, thus may restricting to be used. Here, we describe a novel human-derived CPP, denoted hPP10, and hPP10 has cell-penetrating properties evaluated by CellPPD web server, as well as In-Vitro and In-Vivo analysis. In vitro studies showed that hPP10-FITC was able to penetrate into various cells including primary cultured cells, likely through an endocytosis pathway. And functionalized macromolecules, such as green fluorescent protein (GFP), tumor-specific apoptosis inducer Apoptin as well as biological active enzyme GCLC (Glutamate-cysteine ligase, catalytic subunit) can be delivered by hPP10 in vitro and in vivo. Collectively, our results suggest that hPP10 provide a novel and versatile tool to deliver exogenous proteins or drugs for clinical applications as well as reprogrammed cell-based therapy. |
format | Online Article Text |
id | pubmed-5226491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52264912017-01-18 Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis Wang, Hu Ma, Jie-Lan Yang, Ying-Gui Song, Yang Wu, Jiao Qin, Yan-Yan Zhao, Xue-Li Wang, Jun Zou, Li-Li Wu, Jiang-Feng Li, Jun-Ming Liu, Chang-Bai Oncotarget Research Paper Cell-penetrating peptide (CPP) based delivery have provided immense potential for the therapeutic applications, however, most of nonhuman originated CPPs carry the risk of possible cytotoxicity and immunogenicity, thus may restricting to be used. Here, we describe a novel human-derived CPP, denoted hPP10, and hPP10 has cell-penetrating properties evaluated by CellPPD web server, as well as In-Vitro and In-Vivo analysis. In vitro studies showed that hPP10-FITC was able to penetrate into various cells including primary cultured cells, likely through an endocytosis pathway. And functionalized macromolecules, such as green fluorescent protein (GFP), tumor-specific apoptosis inducer Apoptin as well as biological active enzyme GCLC (Glutamate-cysteine ligase, catalytic subunit) can be delivered by hPP10 in vitro and in vivo. Collectively, our results suggest that hPP10 provide a novel and versatile tool to deliver exogenous proteins or drugs for clinical applications as well as reprogrammed cell-based therapy. Impact Journals LLC 2016-04-11 /pmc/articles/PMC5226491/ /pubmed/27081693 http://dx.doi.org/10.18632/oncotarget.8682 Text en Copyright: © 2016 Wang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wang, Hu Ma, Jie-Lan Yang, Ying-Gui Song, Yang Wu, Jiao Qin, Yan-Yan Zhao, Xue-Li Wang, Jun Zou, Li-Li Wu, Jiang-Feng Li, Jun-Ming Liu, Chang-Bai Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis |
title | Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis |
title_full | Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis |
title_fullStr | Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis |
title_full_unstemmed | Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis |
title_short | Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosis |
title_sort | efficient therapeutic delivery by a novel cell-permeant peptide derived from kdm4a protein for antitumor and antifibrosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226491/ https://www.ncbi.nlm.nih.gov/pubmed/27081693 http://dx.doi.org/10.18632/oncotarget.8682 |
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