Zhao Jing, Zang Fengling, Huo Xiaoya, Zheng Shengzhe
Department of Neurology, Affiliated Hospital of Yanbian University, Yanbian Korean Autonomous Prefecture, Jilin, China.
Front Neurol. 2023 Nov 6;14:1292160. doi: 10.3389/fneur.2023.1292160. eCollection 2023.
Glioma is a malignant brain tumor with a high mortality rate; hence novel treatment approaches are being explored to improve patient outcomes. Ferroptosis, a newly described form of regulated cell death, is emerging as a potential therapeutic target in glioma. Ferroptosis is characterized by the accumulation of lipid peroxides due to a loss of intracellular antioxidant systems represented by the depletion of glutathione and decreased activity of glutathione peroxidase 4 (GPX4). Since glioma cells have a high demand for iron and lipid metabolism, modulation of ferroptosis may represent a promising therapeutic approach for this malignancy. Recent studies indicate that ferroptosis inducers like erastin and RSL3 display potent anticancer activity in a glioma model. In addition, therapeutic strategies, including GPX4 targeting, lipid metabolism modulation, inhibition of amino acid transporters, and ferroptosis targeting natural compounds, have shown positive results in preclinical studies. This review will provide an overview of the functions of ferroptosis in glioma and its potential as a suitable target for glioma therapy.
胶质瘤是一种死亡率很高的恶性脑肿瘤;因此,人们正在探索新的治疗方法以改善患者的预后。铁死亡是一种新描述的程序性细胞死亡形式,正成为胶质瘤潜在的治疗靶点。铁死亡的特征是由于以谷胱甘肽耗竭和谷胱甘肽过氧化物酶4(GPX4)活性降低为代表的细胞内抗氧化系统丧失,导致脂质过氧化物积累。由于胶质瘤细胞对铁和脂质代谢有很高的需求,调节铁死亡可能是治疗这种恶性肿瘤的一种有前景的方法。最近的研究表明,如erastin和RSL3等铁死亡诱导剂在胶质瘤模型中显示出强大的抗癌活性。此外,包括靶向GPX4、调节脂质代谢、抑制氨基酸转运体以及靶向铁死亡的天然化合物等治疗策略,在临床前研究中已显示出积极的结果。本综述将概述铁死亡在胶质瘤中的作用及其作为胶质瘤治疗合适靶点的潜力。