International Journal of Nanomedicine · 2020 · 82 citations · 24 references
PharmacyMedicinal ChemistryOncologyDna RepairMolecular OncologyTargeted Drug DeliveryCancer NanomedicineGlioblastomaNanomedicineNanoparticle DesignTargeted Cancer TherapyTargeted TherapyBrain Targeting LigandsCancer NanotherapyDna Damage Repair PathwaysEgfr InhibitionEpidermal Growth Factor Receptor Targeting LigandsGlioblastoma Drug TherapyGlioblastoma Targeted TherapyTumor Targeting Ligands
PURPOSE: In this study, we constructed novel brain-targeting complexes (U2-AuNP) by conjugating aptamer U2 to the gold nanoparticle (AuNPs) surface as a promising option for GBM therapy. MATERIALS AND METHODS: The properties of the U2-AuNP complexes were thoroughly characterized. Then, we detected the in vitro effects of U2-AuNP in U87-EGFRvIII cell lines and the in vivo antitumor effects of U2-AuNP in GBM-bearing mice. Furthermore, we explored the inhibition mechanism of U2-AuNP in U87-EGFRvIII cell lines. RESULTS: We found that U2-AuNP inhibits the proliferation and invasion of U87-EGFRvIII cell lines and prolongs the survival time of GBM-bearing mice. We found that U2-AuNP can inhibit the EGFR-related pathway and prevent DNA damage repair in GBM cells. CONCLUSION: These results reveal the promising potential of U2-AuNP as a drug candidate for targeted therapy in GBM.
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Donald M. O’Rourke, MacLean P. Nasrallah, Arati Desai et al. · Science Translational Medicine · 2017 · 1.8K citations · Full text
Medicine, Immunology, Oncology +17
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Medicine, Cancer Biology, Oncology +17