Falone Stefano, Santini Silvano, Cordone Valeria, Di Emidio Giovanna, Tatone Carla, Cacchio Marisa, Amicarelli Fernanda
Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Department of Neurosciences, Imaging and Clinical Sciences, University "G. d'Annunzio", Chieti, Italy.
Front Public Health. 2018 Feb 23;6:33. doi: 10.3389/fpubh.2018.00033. eCollection 2018.
Electrical devices currently used in clinical practice and common household equipments generate extremely low-frequency magnetic fields (ELF-MF) that were classified by the International Agency for Research on Cancer as "possible carcinogenic." Assuming that ELF-MF plays a role in the carcinogenic process without inducing direct genomic alterations, ELF-MF may be involved in the promotion or progression of cancers. In particular, ELF-MF-induced responses are suspected to activate redox-responsive intracellular signaling or detoxification scavenging systems. In fact, improved protection against oxidative stress and redox-active xenobiotics is thought to provide critical proliferative and survival advantage in tumors. On this basis, an ever-growing research activity worldwide is attempting to establish whether tumor cells may develop multidrug resistance through the activation of essential cytoprotective networks in the presence of ELF fields, and how this might trigger relevant changes in tumor phenotype. This review builds a framework around how the activity of redox-responsive mediators may be controlled by co-exposure to ELF-MF and reactive oxygen species-generating agents in tumor and cancer cells, in order to clarify whether and how such potential molecular targets could help to minimize or neutralize the functional interaction between ELF-MF and malignancies.
目前临床实践中使用的电气设备和常见家用设备会产生极低频磁场(ELF-MF),国际癌症研究机构将其归类为“可能致癌”。假设ELF-MF在致癌过程中发挥作用而不引起直接的基因组改变,那么ELF-MF可能参与癌症的促进或进展。特别是,怀疑ELF-MF诱导的反应会激活氧化还原反应性细胞内信号传导或解毒清除系统。事实上,增强对氧化应激和具有氧化还原活性的外源性物质的保护作用被认为能为肿瘤提供关键的增殖和生存优势。在此基础上,全球范围内越来越多的研究活动试图确定肿瘤细胞在ELF场存在的情况下是否可能通过激活关键的细胞保护网络产生多药耐药性,以及这可能如何引发肿瘤表型的相关变化。本综述围绕肿瘤细胞和癌细胞中氧化还原反应性介质的活性如何通过同时暴露于ELF-MF和产生活性氧的试剂来控制构建了一个框架,以阐明此类潜在分子靶点是否以及如何有助于最小化或中和ELF-MF与恶性肿瘤之间的功能相互作用。