A Systematic Review of Nanoparticle-Mediated Ferroptosis in Glioma Therapy
Year: 2025
Type: review
Abstract: Lin Jing, Wenguang Xiao, Zhouxing Hu, Xu Liu, Mingqing Yuan Guangxi Key Laboratory of Special Biomedicine; School of Medicine, Guangxi University, Nanning, 530004, People’s Republic of ChinaCorrespondence: Mingqing Yuan, School of Medicine, Guangxi University, Nanning, 530004, People’s Republic of China, Email [email protected] Xu Liu, School of Medicine, Guangxi University, Nanning, 530004, People’s Republic of China, Email [email protected]: Glioma, a highly malignant central nervous system tumor, exhibits aggressive invasiveness, extensive infiltration, and poor prognosis. Conventional treatments such as surgery, radiotherapy, and chemotherapy are hindered by limitations including the inability to overcome the blood-brain barrier (BBB), drug resistance, and high recurrence rates. Ferroptosis induced by nanoparticle-based systems offers an innovative strategy for glioma therapy by efficiently traversing the BBB, precisely delivering ferroptosis inducers, enhancing tumor accumulation, and enabling stimuli-responsive drug release. These features collectively improve the induction efficiency of ferroptosis in glioma cells. Various nanoplatforms, including inorganic nanoparticles, biomimetic carriers, and polymer-based systems, have demonstrated potential in crossing the BBB, inducing ferroptosis, and suppressing glioma progression. These systems enhance reactive oxygen species generation, deplete glutathione, and disrupt tumor microenvironment defense mechanisms, achieving synergistic therapeutic effects. The integration of ferroptosis with nanotechnology is emerging as a promising, non-invasive strategy for the treatment of gliomas, offering substantial therapeutic potential.Keywords: ferroptosis, glioma, nanoplatforms, synergy
Authors: Jing L, Xiao W, Hu Z, Liu X, Yuan M
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W6996942281
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