Ferroptosis-related signaling pathways in cancer drug resistance.

IF 4.6 Q1 ONCOLOGY 癌症耐药(英文) Pub Date : 2025-01-06 eCollection Date: 2025-01-01 DOI:10.20517/cdr.2024.151
Yang Yang, Simin Yu, Wanyao Liu, Yi Zhuo, Chunrun Qu, Yu Zeng
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Abstract

Ferroptosis is an iron-dependent form of programmed cell death induced by lipid peroxidation. This process is regulated by signaling pathways associated with redox balance, iron metabolism, and lipid metabolism. Cancer cells' increased iron demand makes them especially susceptible to ferroptosis, significantly influencing cancer development, therapeutic response, and metastasis. Recent findings indicate that cancer cells can evade ferroptosis by downregulating key signaling pathways related to this process, contributing to drug resistance. This underscores the possibility of modulating ferroptosis as an approach to counteract drug resistance and enhance therapeutic efficacy. This review outlines the signaling pathways involved in ferroptosis and their interactions with cancer-related signaling pathways. We also highlight the current understanding of ferroptosis in cancer drug resistance, offering insights into how targeting ferroptosis can provide novel therapeutic approaches for drug-resistant cancers. Finally, we explore the potential of ferroptosis-inducing compounds and examine the challenges and opportunities for drug development in this evolving field.

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肿瘤耐药中凋亡相关信号通路的研究。
铁下垂是一种铁依赖性的程序性细胞死亡形式,由脂质过氧化引起。这一过程受与氧化还原平衡、铁代谢和脂质代谢相关的信号通路调控。癌细胞对铁的需求增加使它们特别容易发生铁下垂,这对癌症的发展、治疗反应和转移有显著影响。最近的研究表明,癌细胞可以通过下调与这一过程相关的关键信号通路来逃避铁下垂,从而导致耐药性。这强调了调节铁下垂作为一种对抗耐药和提高治疗效果的方法的可能性。本文综述了铁下垂的信号通路及其与癌症相关信号通路的相互作用。我们还强调了目前对铁下垂在癌症耐药中的理解,提供了针对铁下垂如何为耐药癌症提供新的治疗方法的见解。最后,我们探讨了诱导铁中毒化合物的潜力,并研究了在这一不断发展的领域中药物开发的挑战和机遇。
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