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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...

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Detalles Bibliográficos
Autores principales: Zhao, Ming, Zhao, Mengnan, Fu, Chen, Yu, Yang, Fu, Ailing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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.
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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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