Ghasempour Alireza, Tokallou Mohammad Amin, Naderi Allaf Mohammad Reza, Moradi Mohsen, Dehghan Hamideh, Sedighi Mahsa, Shahbazi Mohammad-Ali, Lavi Arab Fahimeh
Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Beilstein J Nanotechnol. 2025 Aug 14;16:1325-1349. doi: 10.3762/bjnano.16.97. eCollection 2025.
Ferroptosis has shown potential therapeutic effects in tumor therapy as an iron-dependent programmed cell death. The induction of ferroptosis is based on lipid peroxidation, the accumulation of iron and reactive oxygen species, and the depletion of glutathione. Nowadays, various nanoparticles are reported for ferroptosis-based therapy. Among them, engineered liposomes have received more attention due to their biocompatibility, low immunogenicity, and flexibility in chemical and structural modifications. The present review focuses on the mechanisms of ferroptosis and its induction by engineered liposomes to improve tumor therapy. It also highlights the fascinating outcome of liposome-mediated ferroptosis in overcoming the obstacles to cancer therapy, along with the limitations and possible future directions.
铁死亡作为一种铁依赖性程序性细胞死亡,在肿瘤治疗中已显示出潜在的治疗效果。铁死亡的诱导基于脂质过氧化、铁和活性氧的积累以及谷胱甘肽的消耗。如今,有多种纳米颗粒被报道用于基于铁死亡的治疗。其中,工程化脂质体因其生物相容性、低免疫原性以及在化学和结构修饰方面的灵活性而受到更多关注。本综述重点关注铁死亡的机制及其由工程化脂质体诱导以改善肿瘤治疗的情况。它还强调了脂质体介导的铁死亡在克服癌症治疗障碍方面的迷人成果,以及局限性和可能的未来方向。