Institute of Biochemistry I, Faculty of Medicine, Goethe-University Frankfurt, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Department of Chemistry and Biochemistry, University of Arizona, 1306 E. University Blvd., Tucson, AZ 85721-0041, USA.
Int J Mol Sci. 2019 Jan 11;20(2):273. doi: 10.3390/ijms20020273.
Iron is an essential element for virtually all organisms. On the one hand, it facilitates cell proliferation and growth. On the other hand, iron may be detrimental due to its redox abilities, thereby contributing to free radical formation, which in turn may provoke oxidative stress and DNA damage. Iron also plays a crucial role in tumor progression and metastasis due to its major function in tumor cell survival and reprogramming of the tumor microenvironment. Therefore, pathways of iron acquisition, export, and storage are often perturbed in cancers, suggesting that targeting iron metabolic pathways might represent opportunities towards innovative approaches in cancer treatment. Recent evidence points to a crucial role of tumor-associated macrophages (TAMs) as a source of iron within the tumor microenvironment, implying that specifically targeting the TAM iron pool might add to the efficacy of tumor therapy. Here, we provide a brief summary of tumor cell iron metabolism and updated molecular mechanisms that regulate cellular and systemic iron homeostasis with regard to the development of cancer. Since iron adds to shaping major hallmarks of cancer, we emphasize innovative therapeutic strategies to address the iron pool of tumor cells or cells of the tumor microenvironment for the treatment of cancer.
铁是几乎所有生物体必需的元素。一方面,它促进细胞增殖和生长。另一方面,由于其氧化还原能力,铁可能有害,从而导致自由基形成,进而可能引发氧化应激和 DNA 损伤。由于铁在肿瘤细胞存活和肿瘤微环境重编程中的主要功能,铁在肿瘤进展和转移中也起着至关重要的作用。因此,癌症中经常会干扰铁摄取、输出和储存的途径,这表明针对铁代谢途径可能是癌症治疗创新方法的机会。最近的证据表明,肿瘤相关巨噬细胞 (TAM) 是肿瘤微环境中铁的重要来源,这意味着专门针对 TAM 的铁池可能会增加肿瘤治疗的效果。在这里,我们简要总结了肿瘤细胞的铁代谢以及调节细胞和系统铁稳态的最新分子机制,这些机制与癌症的发展有关。由于铁有助于塑造癌症的主要特征,我们强调创新的治疗策略,以解决肿瘤细胞或肿瘤微环境细胞的铁池,用于癌症的治疗。