ArticleMolecular biology reports2026
Biogenic Cu-Fe bimetallic nanoparticles induce apoptosis and inhibit invasion in glioblastoma cells.
Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundThis study demonstrates the wide-ranging therapeutic potential of copper-iron (Cu-Fe) bimetallic nanoparticles (BNPs), which were synthesized using an environmentally friendly method involving Corylus avellana leaf extract. METHODS AND
resultsFollowing phytochemical profiling of the aqueous extract via LC-MS/MS, the Cu-Fe BNPs were characterized and confirmed to be stable nanostructures with an average size of 20-30 nm. Biological evaluations revealed selective cytotoxicity against U87-MG glioblastoma cells, with IC₅₀ values of 11.8 µg/mL and 325 µg/mL for U87-MG and HDF cells respectively, resulting in a selectivity index (SI) of 27.54. Hoechst 33,258 staining revealed an increased number of nuclear abnormalities in glioblastoma cells. Real-time PCR analysis revealed a 12.21-fold increase in BAX expression at 100 µg/mL and a 0.10-fold decrease in BCL2 expression at 200 µg/mL. This resulted in a maximum BAX/BCL2 ratio of 20.18, which supports the activation of the intrinsic apoptotic pathway. Furthermore, Cu-Fe BNPs suppressed glioblastoma cell migration in a dose-dependent manner, reducing wound closure from 55.1% to 10.6% after 24 h at 400 µg/mL. Antibacterial analysis revealed a decrease in the viability of Pseudomonas aeruginosa and Staphylococcus aureus to 25.3% and 27.0%, respectively, at 400 µg/mL.
conclusionsCu-Fe BNPs exhibited selective anticancer, pro-apoptotic, anti-migratory, and antibacterial activities, indicating their potential as multifunctional nanotherapeutic agents for glioblastoma treatment.
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