Effect of gold-conjugated resveratrol nanoparticles on glioma cells and its underlying mechanism.
Biomed Mater Eng
; 35(3): 279-292, 2024.
Article
em En
| MEDLINE
| ID: mdl-38461500
ABSTRACT
BACKGROUND:
Glioblastoma is the most aggressive brain tumor with poor prognosis. Although Resveratrol (Rsv) is known to have therapeutic effects on glioma, the effects of gold-conjugated resveratrol nanoparticles (Rsv-AuNPs) on glioma cells are rarely reported.OBJECTIVE:
We aimed to investigate the effects of Rsv-AuNPs on glioma cells and its underlying mechanism.METHOD:
Human glioma cell line U87 was treated with different concentrations of Rsv-AuNPs. CCK-8, transwell, and wound healing assay were performed to measure the effects of Rsv-AuNPs on cell proliferation, invasion, and migration ability, respectively. Flow cytometry assay was used to detect the effects of Rsv-AuNPs on apoptosis. Changes of protein expressions related to proliferation, invasion, migration, and apoptosis were measured by Western blot assay. In addition, the inhibitory role of Rsv-AuNPs in the PI3K/AKT/mTOR signaling pathway was verified by using PI3K inhibitor LY294002.RESULTS:
Rsv-AuNPs treatment significantly suppressed proliferation, migration, and invasion of U87 cells (all P < 0.05) and increased the apoptosis rate (P < 0.05). The changes of proteins related to proliferation, migration, invasion and apoptosis were consistent (all P < 0.05). Moreover, Rsv-AuNPs treatment significantly inhibited the phosphorylation of PI3K, AKT and mTOR proteins in U87 cells (P < 0.05).CONCLUSION:
The present study found that Rsv-AuNPs inhibited the proliferation, migration, and invasion of U87 cells and induced apoptosis by inhibiting the activation of PI3K/AKT/mTOR signaling pathway. In the future, Rsv-AuNPs might be applied to the clinical treatment of glioma through more in-depth animal and clinical research.Palavras-chave
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Base de dados:
MEDLINE
Assunto principal:
Movimento Celular
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Apoptose
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Proliferação de Células
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Nanopartículas Metálicas
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Resveratrol
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Glioma
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Ouro
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article