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癌症中AMPK与铁死亡的分析:一个潜在的调控轴

An Analysis of AMPK and Ferroptosis in Cancer: A Potential Regulatory Axis.

作者信息

Zhang Ting, Wang Xi, Alexander Peter G, Feng Peng, Zhang Jianying

机构信息

Department of Orthopaedic Surgery, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Department of Trauma Orthopedics, The First Affiliated Hospital of Xinjiang Medical University, 830011 Urumqi, Xinjiang, China.

出版信息

Front Biosci (Landmark Ed). 2025 Jul 30;30(7):36618. doi: 10.31083/FBL36618.

Abstract

Adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) is an energy homeostasis controller that regulates various metabolic pathways to promote adenosine triphosphate (ATP) generation and suppress energy expenditure, thereby restoring energy homeostasis. As a co-factor in many enzymes, iron is an essential mineral for maintaining ATP levels in our bodies. Ferroptosis is an iron-dependent mode of cell death that occurs in various pathological processes, including cancer, metabolic disorders, and autoimmune diseases, by regulating iron metabolism, lipoperoxidation, and anti-oxidation functions. Ferroptosis is triggered by oxidative and energy stress, both controlled by cancer-associated signaling pathways. Emerging studies have demonstrated that AMPK directly influences ferroptosis by modulating lipid metabolism, redox homeostasis, and iron transport. Cancer cells exhibiting elevated baseline AMPK activity demonstrate resistance to ferroptosis, whereas AMPK suppression enhances their susceptibility to this regulated form of cell death. While the precise mechanistic details are yet to be fully elucidated, accumulating evidence suggests that AMPK-mediated ferroptosis regulation may contribute to cancer development and therapeutic responses. This review summarizes recent advances in understanding the interplay between AMPK and ferroptosis in cancer biology and discusses the potential of targeting the AMPK-ferroptosis axis for innovative anticancer strategies.

摘要

5'-单磷酸腺苷(AMP)激活的蛋白激酶(AMPK)是一种能量稳态控制器,它调节各种代谢途径以促进三磷酸腺苷(ATP)的生成并抑制能量消耗,从而恢复能量稳态。作为许多酶的辅助因子,铁是维持我们身体ATP水平所必需的矿物质。铁死亡是一种铁依赖性的细胞死亡方式,通过调节铁代谢、脂质过氧化和抗氧化功能,发生在包括癌症、代谢紊乱和自身免疫性疾病在内的各种病理过程中。铁死亡由氧化应激和能量应激触发,二者均受癌症相关信号通路的控制。新兴研究表明,AMPK通过调节脂质代谢、氧化还原稳态和铁转运直接影响铁死亡。基线AMPK活性升高的癌细胞对铁死亡具有抗性,而抑制AMPK则会增强它们对这种受调控的细胞死亡形式的敏感性。虽然确切的机制细节尚未完全阐明,但越来越多的证据表明,AMPK介导的铁死亡调节可能有助于癌症的发展和治疗反应。本综述总结了在癌症生物学中理解AMPK与铁死亡之间相互作用的最新进展,并讨论了针对AMPK-铁死亡轴制定创新抗癌策略的潜力。

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