Lee Jaewang, Roh Jong-Lyel
Department of Otorhinolaryngology-Head and Neck Surgery, CHA Bundang Medical Center, CHA University, Seongnam, Gyeonggi-Do, 13496, Republic of Korea.
Department of Biomedical Science, General Graduate School, CHA University, Pocheon, Republic of Korea.
Cancer Metastasis Rev. 2025 Feb 25;44(1):36. doi: 10.1007/s10555-025-10252-8.
Ferroptosis, an iron-dependent form of cell death, has been the focus of extensive research over the past decade, leading to the elucidation of key molecules and mechanisms involved in this process. While several studies have highlighted iron sources for the Fenton reaction, the predominant mechanism for iron release in ferroptosis has been identified as ferritinophagy, which occurs in response to iron starvation. However, much of the existing literature has concentrated on lipid peroxidation rather than on the mechanisms of iron release. This review proposes three distinct mechanisms of iron mobilization: ferritinophagy, reductive pathways with selective gating of ferritin pores, and quinone-mediated iron mobilization. Notably, the latter two mechanisms operate independently of iron starvation and rely primarily on reductants such as NADH and O•. The inhibition of the respiratory chain, particularly under the activation of α-ketoglutarate dehydrogenase, leads to the accumulation of these reductants, which in turn promotes iron release from ferritin and indirectly inhibits AMP-activated protein kinase through excessive iron levels. In this work, we delineate the intricate relationship between iron mobilization and bioenergetic processes under conditions of oxidative stress. Furthermore, this review aims to enhance the understanding of the connections between ferroptosis and these mechanisms.
铁死亡是一种铁依赖性的细胞死亡形式,在过去十年中一直是广泛研究的焦点,这使得参与该过程的关键分子和机制得以阐明。虽然几项研究强调了芬顿反应的铁来源,但铁死亡中铁释放的主要机制已被确定为铁自噬,它发生在对铁饥饿的反应中。然而,现有文献大多集中在脂质过氧化而非铁释放机制上。本综述提出了三种不同的铁动员机制:铁自噬、铁蛋白孔选择性门控的还原途径和醌介导的铁动员。值得注意的是,后两种机制独立于铁饥饿起作用,主要依赖于NADH和O•等还原剂。呼吸链的抑制,特别是在α-酮戊二酸脱氢酶激活的情况下,会导致这些还原剂的积累,进而促进铁从铁蛋白中释放,并通过过量的铁水平间接抑制AMP激活的蛋白激酶。在这项工作中,我们描绘了氧化应激条件下铁动员与生物能量过程之间的复杂关系。此外,本综述旨在增进对铁死亡与这些机制之间联系的理解。