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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
Descripción
Sumario: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.