Crescenzi Elvira, Leonardi Antonio, Pacifico Francesco
Istituto per l'Endocrinologia e l'Oncologia Sperimentale, CNR, Via S. Pansini, 5, 80131 Naples, Italy.
Dipartimento di Medicina Molecolare e Biotecnologie Mediche, "Federico II" University of Naples, Via S. Pansini, 5, 80131 Naples, Italy.
Biology (Basel). 2023 Jul 11;12(7):989. doi: 10.3390/biology12070989.
Iron participates in a number of biological processes and plays a crucial role in cellular homeostasis. Alterations in iron metabolism are considered hallmarks of cancer and drivers of aggressive behaviors, such as uncontrolled proliferation, resistance to apoptosis, enhanced metastatic ability, increased cell plasticity and stemness. Furthermore, a dysregulated iron metabolism has been associated with the development of an adverse tumor microenvironment. Alterations in iron metabolism have been described in cellular senescence and in aging. For instance, iron has been shown to accumulate in aged tissues and in age-related diseases. Furthermore, in vitro studies demonstrate increases in iron content in both replicative and stress-induced senescent cells. However, the role, the mechanisms of regulation and dysregulation and the effects of iron metabolism on senescence remain significantly less characterized. In this review, we first provide an overview of iron metabolism and iron regulatory proteins. Then, we summarize alterations in iron homeostasis in cancer and senescence from a cellular point of view.
铁参与多种生物过程,在细胞内稳态中发挥关键作用。铁代谢的改变被认为是癌症的标志以及侵袭性行为的驱动因素,如不受控制的增殖、对细胞凋亡的抵抗、转移能力增强、细胞可塑性和干性增加。此外,铁代谢失调与不良肿瘤微环境的形成有关。细胞衰老和衰老过程中均已描述了铁代谢的改变。例如,铁已被证明会在衰老组织和与年龄相关的疾病中积累。此外,体外研究表明,复制性衰老细胞和应激诱导的衰老细胞中的铁含量均会增加。然而,铁代谢在衰老中的作用、调节和失调机制以及影响仍显著缺乏特征描述。在本综述中,我们首先概述铁代谢和铁调节蛋白。然后,我们从细胞角度总结癌症和衰老中铁稳态的改变。