Liu Xingyu, Tuerxun Halahati, Zhao Yixin, Li Yawen, Wen Shuhui, Li Xi, Zhao Yuguang
Cancer Center, The First Hospital of Jilin University, Changchun, 130021, China.
J Transl Med. 2025 Jan 6;23(1):18. doi: 10.1186/s12967-024-06059-w.
Ferroptosis and autophagy are two main forms of regulated cell death (RCD). Ferroptosis is a newly identified RCD driven by iron accumulation and lipid peroxidation. Autophagy is a self-degradation system through membrane rearrangement. Autophagy regulates the metabolic balance between synthesis, degradation and reutilization of cellular substances to maintain intracellular homeostasis. Numerous studies have demonstrated that both ferroptosis and autophagy play important roles in cancer pathogenesis and cancer therapy. We also found that there are intricate connections between ferroptosis and autophagy. In this article, we tried to clarify how different kinds of autophagy participate in the process of ferroptosis and sort out the common regulatory pathways between ferroptosis and autophagy in cancer. By exploring the complex crosstalk between ferroptosis and autophagy, we hope to broaden horizons of cancer therapy.
铁死亡和自噬是调节性细胞死亡(RCD)的两种主要形式。铁死亡是一种新发现的由铁积累和脂质过氧化驱动的RCD。自噬是一种通过膜重排的自我降解系统。自噬调节细胞物质合成、降解和再利用之间的代谢平衡,以维持细胞内稳态。大量研究表明,铁死亡和自噬在癌症发病机制和癌症治疗中都发挥着重要作用。我们还发现铁死亡和自噬之间存在复杂的联系。在本文中,我们试图阐明不同类型的自噬如何参与铁死亡过程,并梳理癌症中铁死亡和自噬之间的共同调控途径。通过探索铁死亡和自噬之间复杂的相互作用,我们希望拓宽癌症治疗的视野。