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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...

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Autores principales: 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
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
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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.
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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
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