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Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells
Surgery and radiotherapy cannot fully remove brain glioma; thus, chemotherapy continues to play an important role in treatment of this illness. However, because of the restriction of the blood-brain barrier (BBB) and the regeneration of glioma stem cells, post-chemotherapy relapse usually occurs. He...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471209/ https://www.ncbi.nlm.nih.gov/pubmed/28615716 http://dx.doi.org/10.1038/s41598-017-03805-7 |
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author | Mu, Li-Min Bu, Ying-Zi Liu, Lei Xie, Hong-Jun Ju, Rui-Jun Wu, Jia-Shuan Zeng, Fan Zhao, Yao Zhang, Jing-Ying Lu, Wan-Liang |
author_facet | Mu, Li-Min Bu, Ying-Zi Liu, Lei Xie, Hong-Jun Ju, Rui-Jun Wu, Jia-Shuan Zeng, Fan Zhao, Yao Zhang, Jing-Ying Lu, Wan-Liang |
author_sort | Mu, Li-Min |
collection | PubMed |
description | Surgery and radiotherapy cannot fully remove brain glioma; thus, chemotherapy continues to play an important role in treatment of this illness. However, because of the restriction of the blood-brain barrier (BBB) and the regeneration of glioma stem cells, post-chemotherapy relapse usually occurs. Here, we report a potential solution to these issues that involves a type of novel multifunctional vinblastine liposomes equipped with transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8). Studies were performed on brain glioma and glioma stem cells in vitro and were verified in brain glioma-bearing mice. The liposomes were transported across the BBB, killing brain glioma and glioma stem cells via the induction of necrosis, apoptosis and autophagy. Furthermore, we reveal the molecular mechanisms for treating brain glioma and glioma stem cells via functionalized drug lipid vesicles. |
format | Online Article Text |
id | pubmed-5471209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54712092017-06-19 Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells Mu, Li-Min Bu, Ying-Zi Liu, Lei Xie, Hong-Jun Ju, Rui-Jun Wu, Jia-Shuan Zeng, Fan Zhao, Yao Zhang, Jing-Ying Lu, Wan-Liang Sci Rep Article Surgery and radiotherapy cannot fully remove brain glioma; thus, chemotherapy continues to play an important role in treatment of this illness. However, because of the restriction of the blood-brain barrier (BBB) and the regeneration of glioma stem cells, post-chemotherapy relapse usually occurs. Here, we report a potential solution to these issues that involves a type of novel multifunctional vinblastine liposomes equipped with transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8). Studies were performed on brain glioma and glioma stem cells in vitro and were verified in brain glioma-bearing mice. The liposomes were transported across the BBB, killing brain glioma and glioma stem cells via the induction of necrosis, apoptosis and autophagy. Furthermore, we reveal the molecular mechanisms for treating brain glioma and glioma stem cells via functionalized drug lipid vesicles. Nature Publishing Group UK 2017-06-14 /pmc/articles/PMC5471209/ /pubmed/28615716 http://dx.doi.org/10.1038/s41598-017-03805-7 Text en © The Author(s) 2017 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 Mu, Li-Min Bu, Ying-Zi Liu, Lei Xie, Hong-Jun Ju, Rui-Jun Wu, Jia-Shuan Zeng, Fan Zhao, Yao Zhang, Jing-Ying Lu, Wan-Liang Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells |
title | Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells |
title_full | Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells |
title_fullStr | Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells |
title_full_unstemmed | Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells |
title_short | Lipid vesicles containing transferrin receptor binding peptide TfR-T(12) and octa-arginine conjugate stearyl-R(8) efficiently treat brain glioma along with glioma stem cells |
title_sort | lipid vesicles containing transferrin receptor binding peptide tfr-t(12) and octa-arginine conjugate stearyl-r(8) efficiently treat brain glioma along with glioma stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471209/ https://www.ncbi.nlm.nih.gov/pubmed/28615716 http://dx.doi.org/10.1038/s41598-017-03805-7 |
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