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Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes
BACKGROUND: Glioma is the most aggressive and lethal brain tumor in humans, it comprises about 30 per cent of all brain tumors and central nervous system tumors. PURPOSE: The objective of this study was to create novel brain-targeting nanoliposomes to encapsulate curcumin as a promising option for g...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858816/ https://www.ncbi.nlm.nih.gov/pubmed/29588587 http://dx.doi.org/10.2147/IJN.S157019 |
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author | Zhao, Ming Zhao, Mengnan Fu, Chen Yu, Yang Fu, Ailing |
author_facet | Zhao, Ming Zhao, Mengnan Fu, Chen Yu, Yang Fu, Ailing |
author_sort | Zhao, Ming |
collection | PubMed |
description | BACKGROUND: Glioma is the most aggressive and lethal brain tumor in humans, it comprises about 30 per cent of all brain tumors and central nervous system tumors. PURPOSE: The objective of this study was to create novel brain-targeting nanoliposomes to encapsulate curcumin as a promising option for glioma therapy. PATIENTS AND METHODS: Human glioma cells (U251MG) were used to determine cell uptake efficiency and possible internalization mechanism of the curcumin-loaded nanoliposomes modified by a brain-targeting peptide RDP. In addition, intracranial glioma mice model was prepared by transplantation of U251MG cells into the mice striatum, and then the liposomes were intravenously administered into the glioma-bearing mice to evaluate the anti-glioma activity. RESULTS: RDP-modified liposomes (RCL) could enter the brain and glioma region, and were internalized by the glioma cells perhaps through acetylcholine receptor-mediated endocytosis pathway. Furthermore, the RCL prolonged the survival time of the glioma-bearing mice from 23 to 33 days, and the inhibition mechanism of the RCL on glioma cell was partly due to cell cycle arrest at the S phase and induction of cell apoptosis. CONCLUSION: This study would provide a potential approach for targeted delivery of drug-loaded liposomes for glioma treatment. |
format | Online Article Text |
id | pubmed-5858816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58588162018-03-27 Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes Zhao, Ming Zhao, Mengnan Fu, Chen Yu, Yang Fu, Ailing Int J Nanomedicine Original Research BACKGROUND: Glioma is the most aggressive and lethal brain tumor in humans, it comprises about 30 per cent of all brain tumors and central nervous system tumors. PURPOSE: The objective of this study was to create novel brain-targeting nanoliposomes to encapsulate curcumin as a promising option for glioma therapy. PATIENTS AND METHODS: Human glioma cells (U251MG) were used to determine cell uptake efficiency and possible internalization mechanism of the curcumin-loaded nanoliposomes modified by a brain-targeting peptide RDP. In addition, intracranial glioma mice model was prepared by transplantation of U251MG cells into the mice striatum, and then the liposomes were intravenously administered into the glioma-bearing mice to evaluate the anti-glioma activity. RESULTS: RDP-modified liposomes (RCL) could enter the brain and glioma region, and were internalized by the glioma cells perhaps through acetylcholine receptor-mediated endocytosis pathway. Furthermore, the RCL prolonged the survival time of the glioma-bearing mice from 23 to 33 days, and the inhibition mechanism of the RCL on glioma cell was partly due to cell cycle arrest at the S phase and induction of cell apoptosis. CONCLUSION: This study would provide a potential approach for targeted delivery of drug-loaded liposomes for glioma treatment. Dove Medical Press 2018-03-15 /pmc/articles/PMC5858816/ /pubmed/29588587 http://dx.doi.org/10.2147/IJN.S157019 Text en © 2018 Zhao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zhao, Ming Zhao, Mengnan Fu, Chen Yu, Yang Fu, Ailing Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
title | Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
title_full | Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
title_fullStr | Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
title_full_unstemmed | Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
title_short | Targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
title_sort | targeted therapy of intracranial glioma model mice with curcumin nanoliposomes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858816/ https://www.ncbi.nlm.nih.gov/pubmed/29588587 http://dx.doi.org/10.2147/IJN.S157019 |
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