Gold nanoparticles-supported iron oxide particles endows bone scaffolds with anti-tumor function

Iron oxide (Fe-O) has anti-tumor properties, due to its ability of catalyzing hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) of tumor cells to generate reactive oxygen species (ROS) and then cause ferroptosis. Its anti-tumor performance is restricted due to insufficient H<sub>2</sub>O<sub>2</sub> in tumor cells. A nanomedicine, Au nanoparticles (NPs) grown on Fe-O, was integrated into poly-l-lactide (PLLA) scaffolds. Results indicated that Au NPs could consume glucose of tumor cells to produce H<sub>2</sub>O<sub>2</sub>, which supplemented reaction substrate. PLLA/Au@Fe-O scaffold showed enhanced anti-tumor activities against MG63, including increased mortality, decreased migration and colony formation. PLLA/Au@Fe-O scaffold promoted ferroptosis in MG63, including up-regulation of COX-2 protein, down-regulation of FTH1 protein and GPX4 protein. PLLA/Au@Fe-O scaffold also promoted autophagy in MG63, including down-regulation of P62 protein, and up-regulation of LC3BII/I. Mechanistically, PLLA/Au@Fe-O scaffold possessed enhanced anti-tumor activities through promoting ferroptosis and autophagy.

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Publication Details

Journal
Free Radical Research
Published
2025-02-01
DOI
https://doi.org/10.1080/10715762.2025.2466246
Citations
1
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
1.52

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article

Gold nanoparticles-supported iron oxide particles endows bone scaffolds with anti-tumor function

Tiantian He, Shuping Peng, Wenjing Yang, Youwen Yang et al.
1 citations
Free Radical Research
Ferroptosis and cancer prognosis
1.52
article

Gold nanoparticles-supported iron oxide particles endows bone scaffolds with anti-tumor function

Tiantian He, Shuping Peng, Wenjing Yang, Youwen Yang, Cijun Shuai
article en
1 citations

Abstract

Iron oxide (Fe-O) has anti-tumor properties, due to its ability of catalyzing hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) of tumor cells to generate reactive oxygen species (ROS) and then cause ferroptosis. Its anti-tumor performance is restricted due to insufficient H<sub>2</sub>O<sub>2</sub> in tumor cells. A nanomedicine, Au nanoparticles (NPs) grown on Fe-O, was integrated into poly-l-lactide (PLLA) scaffolds. Results indicated that Au NPs could consume glucose of tumor cells to produce H<sub>2</sub>O<sub>2</sub>, which supplemented reaction substrate. PLLA/Au@Fe-O scaffold showed enhanced anti-tumor activities against MG63, including increased mortality, decreased migration and colony formation. PLLA/Au@Fe-O scaffold promoted ferroptosis in MG63, including up-regulation of COX-2 protein, down-regulation of FTH1 protein and GPX4 protein. PLLA/Au@Fe-O scaffold also promoted autophagy in MG63, including down-regulation of P62 protein, and up-regulation of LC3BII/I. Mechanistically, PLLA/Au@Fe-O scaffold possessed enhanced anti-tumor activities through promoting ferroptosis and autophagy.

Free Radical ResearchVol. 59(2)
Central South University (CN), Xiangya Hospital Central South University (CN), Jiangxi University of Science and Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 22%
Ferroptosis and cancer prognosis
1.52
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Gold nanoparticles-supported iron oxide particles endows bone scaffolds with anti-tumor function — Tiantian He, Shuping Peng, et al. · Free Radical Research (2025) | TGRS Research Map | TGRS