Liu Xuan, Zhang Yiqian, Wu Xuyi, Xu Fuyan, Ma Hongbo, Wu Mengling, Xia Yong
Department of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
West China School of Pharmacy, Sichuan University, Chengdu, China.
Front Pharmacol. 2022 Jun 30;13:909821. doi: 10.3389/fphar.2022.909821. eCollection 2022.
Ferroptosis is an iron-dependent regulated form of cell death caused by excessive lipid peroxidation. This form of cell death differed from known forms of cell death in morphological and biochemical features such as apoptosis, necrosis, and autophagy. Cancer cells require higher levels of iron to survive, which makes them highly susceptible to ferroptosis. Therefore, it was found to be closely related to the progression, treatment response, and metastasis of various cancer types. Numerous studies have found that the ferroptosis pathway is closely related to drug resistance and metastasis of cancer. Some cancer cells reduce their susceptibility to ferroptosis by downregulating the ferroptosis pathway, resulting in resistance to anticancer therapy. Induction of ferroptosis restores the sensitivity of drug-resistant cancer cells to standard treatments. Cancer cells that are resistant to conventional therapies or have a high propensity to metastasize might be particularly susceptible to ferroptosis. Some biological processes and cellular components, such as epithelial-mesenchymal transition (EMT) and noncoding RNAs, can influence cancer metastasis by regulating ferroptosis. Therefore, targeting ferroptosis may help suppress cancer metastasis. Those progresses revealed the importance of ferroptosis in cancer, In order to provide the detailed molecular mechanisms of ferroptosis in regulating therapy resistance and metastasis and strategies to overcome these barriers are not fully understood, we described the key molecular mechanisms of ferroptosis and its interaction with signaling pathways related to therapy resistance and metastasis. Furthermore, we summarized strategies for reversing resistance to targeted therapy, chemotherapy, radiotherapy, and immunotherapy and inhibiting cancer metastasis by modulating ferroptosis. Understanding the comprehensive regulatory mechanisms and signaling pathways of ferroptosis in cancer can provide new insights to enhance the efficacy of anticancer drugs, overcome drug resistance, and inhibit cancer metastasis.
铁死亡是一种由过量脂质过氧化引起的铁依赖性调节性细胞死亡形式。这种细胞死亡形式在形态和生化特征上与已知的细胞死亡形式如凋亡、坏死和自噬不同。癌细胞需要更高水平的铁来存活,这使得它们对铁死亡高度敏感。因此,发现它与各种癌症类型的进展、治疗反应和转移密切相关。大量研究发现,铁死亡途径与癌症的耐药性和转移密切相关。一些癌细胞通过下调铁死亡途径来降低其对铁死亡的敏感性,从而导致对抗癌治疗产生耐药性。诱导铁死亡可恢复耐药癌细胞对标准治疗的敏感性。对传统疗法耐药或具有高转移倾向的癌细胞可能对铁死亡特别敏感。一些生物学过程和细胞成分,如上皮-间质转化(EMT)和非编码RNA,可以通过调节铁死亡来影响癌症转移。因此,靶向铁死亡可能有助于抑制癌症转移。这些进展揭示了铁死亡在癌症中的重要性。为了详细阐述铁死亡在调节治疗耐药性和转移中的分子机制以及克服这些障碍的策略尚未完全明了,我们描述了铁死亡的关键分子机制及其与治疗耐药性和转移相关信号通路的相互作用。此外,我们总结了通过调节铁死亡来逆转对靶向治疗、化疗、放疗和免疫治疗的耐药性以及抑制癌症转移的策略。了解癌症中铁死亡的综合调节机制和信号通路可以为提高抗癌药物疗效、克服耐药性和抑制癌症转移提供新的见解。