ArticleInternational journal of nanomedicine2025
Multi-Functional Magnetic Nanocrystals for Tumor Mitochondria-Targeted Magnetic Hyperthermia Combined with Enhanced Radiotherapy.
Article in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Spatiotemporal cancer controlNanomedicine (London, England) · 2026Review
- Nanoscale biointerfaces in inter-organelle communication: membrane contact sites, organelle trafficking, and cell fate control.Frontiers in cell and developmental biology · 2026Review
- Clinical Translation of Functional Magnetic Nanoparticles for Intracellular Hyperthermia and Cancer Immunotherapy.International journal of nanomedicine · 2026Review
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: In this study, a fluorescent magnetic nanomaterial with mitochondrial targeting property (Fe Methods: The crystal structure, chemical composition, magnetic properties, optical characteristics and enzyme-like activity of FDLI were systematically elevated. The mitochondrial targeting ability, anti-tumor efficacy, and RT sensitization potential of FDLI were validated in vitro using breast cancer 4T1 cells. Additionally, a subcutaneous breast tumor transplantation mouse model was established to evaluate the therapeutic effectiveness of FDLI, and an optimized in vivo treatment protocol was assessed. Following intravenous administration of FDLI in mice, the diagnostic and therapeutic effects were evaluated using FDLI-mediated multimodal imaging diagnosis and therapeutic strategies. Results: Following mitochondrial targeting of tumor cells, FDLI induced localized TMH and exhibited peroxidase-like activity to generate ·OH, which selectively disrupted the mitochondrial membranes of tumor cells, resulting in reduced adenosine triphosphate (ATP) production and elevated lipid peroxidation. Meanwhile, FDLI increased intracellular reactive oxygen species (ROS) levels while reducing glutathione (GSH) levels, thereby promoting ferroptosis in tumor cells and enhancing the sensitivity to synergistic RT. Conclusion: FDLI can effectively inhibit tumor growth and metastasis, prolonging the survival of tumor-bearing mice through the combined effects of TMH and RT. Our study provides a clinical basis for the development of FDLI as a high-performance agent for integrated tumor diagnosis and therapy.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.