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Therapeutic Approaches with Iron Oxide Nanoparticles to Induce Ferroptosis and Overcome Radioresistance in Cancers.

作者信息

Sant'Angelo Dorianne, Descamps Géraldine, Lecomte Valentin, Stanicki Dimitri, Penninckx Sébastien, Dragan Tatiana, Van Gestel Dirk, Laurent Sophie, Journe Fabrice

机构信息

Department of Human Biology and Toxicology (Cancer Research Unit), Faculty of Medicine, Research Institute for Health Sciences and Technology, University of Mons (UMONS), 7000 Mons, Belgium.

Laboratory of Clinical and Experimental Oncology (LOCE), Institute Jules Bordet, HUB, Université Libre de Bruxelles (ULB), 1070 Brussels, Belgium.

出版信息

Pharmaceuticals (Basel). 2025 Feb 26;18(3):325. doi: 10.3390/ph18030325.


DOI:10.3390/ph18030325
PMID:40143107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11945075/
Abstract

The emergence of nanotechnology in medicine, particularly using iron oxide nanoparticles (IONPs), may impact cancer treatment strategies. IONPs exhibit unique properties, such as superparamagnetism, biocompatibility, and ease of surface modification, making them ideal candidates for imaging, and therapeutic interventions. Their application in targeted drug delivery, especially with traditional chemotherapeutic agents like cisplatin, has shown potential in overcoming limitations such as low bioavailability and systemic toxicity of chemotherapies. Moreover, IONPs, by releasing iron ions, can induce ferroptosis, a form of iron-dependent cell death, which offers a promising pathway to reverse radio- and chemoresistance in cancer therapy. In particular, IONPs demonstrate significant potential as radiosensitisers, enhancing the effects of radiotherapy by promoting reactive oxygen species (ROS) generation, lipid peroxidation, and modulating the tumour microenvironment to stimulate antitumour immune responses. This review explores the multifunctional roles of IONPs in radiosensitisation through ferroptosis induction, highlighting their promise in advancing treatment for head and neck cancers. Additional research is crucial to fully addressing their potential in clinical settings, offering a novel approach to personalised cancer treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/579ec23cb4f2/pharmaceuticals-18-00325-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/dec88e88b527/pharmaceuticals-18-00325-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/89a0d817c437/pharmaceuticals-18-00325-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/4060a80964e3/pharmaceuticals-18-00325-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/648c0129bd8f/pharmaceuticals-18-00325-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/579ec23cb4f2/pharmaceuticals-18-00325-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/dec88e88b527/pharmaceuticals-18-00325-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/89a0d817c437/pharmaceuticals-18-00325-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/4060a80964e3/pharmaceuticals-18-00325-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/648c0129bd8f/pharmaceuticals-18-00325-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/11945075/579ec23cb4f2/pharmaceuticals-18-00325-g004.jpg

相似文献

[1]
Therapeutic Approaches with Iron Oxide Nanoparticles to Induce Ferroptosis and Overcome Radioresistance in Cancers.

Pharmaceuticals (Basel). 2025-2-26

[2]
Amino-modified IONPs potentiates ferroptotic cell death due to the release of Fe ion in the lysosome.

J Environ Sci (China). 2025-4

[3]
Iron Oxide Nanoparticles: Parameters for Optimized Photoconversion Efficiency in Synergistic Cancer Treatment.

J Funct Biomater. 2024-7-25

[4]
Iron oxide nanoparticles induce ferroptosis under mild oxidative stress in vitro.

Sci Rep. 2024-12-28

[5]
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Cureus. 2024-9-16

[6]
Iron oxide nanoparticles cause surface coating- and core chemistry-dependent endothelial cell ferroptosis.

Nanotoxicology. 2022

[7]
MitoTam induces ferroptosis and increases radiosensitivity in head and neck cancer cells.

Radiother Oncol. 2024-11

[8]
Glioblastoma Therapy Using Codelivery of Cisplatin and Glutathione Peroxidase Targeting siRNA from Iron Oxide Nanoparticles.

ACS Appl Mater Interfaces. 2020-9-30

[9]
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Expert Opin Drug Deliv. 2024-6

[10]
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引用本文的文献

[1]
Therapeutic Targeting of Apoptosis, Autophagic Cell Death, Necroptosis, Pyroptosis, and Ferroptosis Pathways in Oral Squamous Cell Carcinoma: Molecular Mechanisms and Potential Strategies.

Biomedicines. 2025-7-16

[2]
Targeting Cancer Cell Fate: Apoptosis, Autophagy, and Gold Nanoparticles in Treatment Strategies.

Curr Issues Mol Biol. 2025-6-14

[3]
Emerging Multifunctional Biomaterials for Addressing Drug Resistance in Cancer.

Biology (Basel). 2025-5-2

本文引用的文献

[1]
Enhancer of Zeste Homolog 2 Protects Mucosal Melanoma from Ferroptosis via the KLF14-SLC7A11 Signaling Pathway.

Cancers (Basel). 2024-10-30

[2]
Temporal evolution and inter-patient heterogeneity in primary and recurrent head and neck squamous cell carcinoma.

BJC Rep. 2024-8-29

[3]
Global radiotherapy demands and corresponding radiotherapy-professional workforce requirements in 2022 and predicted to 2050: a population-based study.

Lancet Glob Health. 2024-12

[4]
Highly Efficient Synergistic Chemotherapy and Magnetic Resonance Imaging for Targeted Ovarian Cancer Therapy Using Hyaluronic Acid-Coated Coordination Polymer Nanoparticles.

Adv Sci (Weinh). 2024-11

[5]
Materials Containing Single-, Di-, Tri-, and Multi-Metal Atoms Bonded to C, N, S, P, B, and O Species as Advanced Catalysts for Energy, Sensor, and Biomedical Applications.

Adv Sci (Weinh). 2024-9

[6]
Therapeutic potentials of FexMoyS-PEG nanoparticles in colorectal cancer: a multimodal approach via ROS-ferroptosis-glycolysis regulation.

J Nanobiotechnology. 2024-5-16

[7]
Superparamagnetic Iron Oxide-Erastin-Polyethylene Glycol Nanotherapeutic Platform: A Ferroptosis-Based Approach for the Integrated Diagnosis and Treatment of Nasopharyngeal Cancer.

Mol Pharm. 2024-6-3

[8]
Diethyldithiocarbamate-ferrous oxide nanoparticles inhibit human and mouse glioblastoma stemness: aldehyde dehydrogenase 1A1 suppression and ferroptosis induction.

Front Pharmacol. 2024-4-24

[9]
Radiation nanomedicines for cancer treatment: a scientific journey and view of the landscape.

EJNMMI Radiopharm Chem. 2024-5-4

[10]
Re-irradiation versus systemic therapy for the management of local-regionally recurrent head and neck cancer.

Radiother Oncol. 2024-7

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