Cargando…
C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma
Chemotherapy of brain glioma faces a major obstacle owing to the inability of drug transport across the blood-brain barrier (BBB). Besides, neovasculatures in brain glioma site result in a rapid infiltration, making complete surgical removal virtually impossible. Herein, we reported a novel kind of...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522305/ https://www.ncbi.nlm.nih.gov/pubmed/28402948 http://dx.doi.org/10.18632/oncotarget.16641 |
_version_ | 1783252145564286976 |
---|---|
author | Wu, Jia-Shuan Mu, Li-Min Bu, Ying-Zi Liu, Lei Yan, Yan Hu, Ying-Jie Bai, Jing Zhang, Jing-Ying Lu, Weiyue Lu, Wan-Liang |
author_facet | Wu, Jia-Shuan Mu, Li-Min Bu, Ying-Zi Liu, Lei Yan, Yan Hu, Ying-Jie Bai, Jing Zhang, Jing-Ying Lu, Weiyue Lu, Wan-Liang |
author_sort | Wu, Jia-Shuan |
collection | PubMed |
description | Chemotherapy of brain glioma faces a major obstacle owing to the inability of drug transport across the blood-brain barrier (BBB). Besides, neovasculatures in brain glioma site result in a rapid infiltration, making complete surgical removal virtually impossible. Herein, we reported a novel kind of C-type natriuretic peptide (CNP) modified vinorelbine lipid vesicles for transferring drug across the BBB, and for treating brain glioma along with disrupting neovasculatures. The studies were performed on brain glioma U87-MG cells in vitro and on glioma-bearing nude mice in vivo. The results showed that the CNP-modified vinorelbine lipid vesicles could transport vinorelbine across the BBB, kill the brain glioma, and destroy neovasculatures effectively. The above mechanisms could be associated with the following aspects, namely, long circulation in the blood; drug transport across the BBB via natriuretic peptide receptor B (NPRB)-mediated transcytosis; elimination of brain glioma cells and disruption of neovasculatures by targeting uptake and cytotoxic injury. Besides, CNP-modified vinorelbine lipid vesicles could induce apoptosis of the glioma cells. The mechanisms could be related to the activations of caspase 8, caspase 3, p53, and reactive oxygen species (ROS), and inhibition of survivin. Hence, CNP-modified lipid vesicles could be used as a carrier material for treating brain glioma and disabling glioma neovasculatures. |
format | Online Article Text |
id | pubmed-5522305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55223052017-08-21 C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma Wu, Jia-Shuan Mu, Li-Min Bu, Ying-Zi Liu, Lei Yan, Yan Hu, Ying-Jie Bai, Jing Zhang, Jing-Ying Lu, Weiyue Lu, Wan-Liang Oncotarget Research Paper Chemotherapy of brain glioma faces a major obstacle owing to the inability of drug transport across the blood-brain barrier (BBB). Besides, neovasculatures in brain glioma site result in a rapid infiltration, making complete surgical removal virtually impossible. Herein, we reported a novel kind of C-type natriuretic peptide (CNP) modified vinorelbine lipid vesicles for transferring drug across the BBB, and for treating brain glioma along with disrupting neovasculatures. The studies were performed on brain glioma U87-MG cells in vitro and on glioma-bearing nude mice in vivo. The results showed that the CNP-modified vinorelbine lipid vesicles could transport vinorelbine across the BBB, kill the brain glioma, and destroy neovasculatures effectively. The above mechanisms could be associated with the following aspects, namely, long circulation in the blood; drug transport across the BBB via natriuretic peptide receptor B (NPRB)-mediated transcytosis; elimination of brain glioma cells and disruption of neovasculatures by targeting uptake and cytotoxic injury. Besides, CNP-modified vinorelbine lipid vesicles could induce apoptosis of the glioma cells. The mechanisms could be related to the activations of caspase 8, caspase 3, p53, and reactive oxygen species (ROS), and inhibition of survivin. Hence, CNP-modified lipid vesicles could be used as a carrier material for treating brain glioma and disabling glioma neovasculatures. Impact Journals LLC 2017-03-29 /pmc/articles/PMC5522305/ /pubmed/28402948 http://dx.doi.org/10.18632/oncotarget.16641 Text en Copyright: © 2017 Wu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wu, Jia-Shuan Mu, Li-Min Bu, Ying-Zi Liu, Lei Yan, Yan Hu, Ying-Jie Bai, Jing Zhang, Jing-Ying Lu, Weiyue Lu, Wan-Liang C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
title | C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
title_full | C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
title_fullStr | C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
title_full_unstemmed | C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
title_short | C-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
title_sort | c-type natriuretic peptide-modified lipid vesicles: fabrication and use for the treatment of brain glioma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522305/ https://www.ncbi.nlm.nih.gov/pubmed/28402948 http://dx.doi.org/10.18632/oncotarget.16641 |
work_keys_str_mv | AT wujiashuan ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT mulimin ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT buyingzi ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT liulei ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT yanyan ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT huyingjie ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT baijing ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT zhangjingying ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT luweiyue ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma AT luwanliang ctypenatriureticpeptidemodifiedlipidvesiclesfabricationanduseforthetreatmentofbrainglioma |