- freely available
Int. J. Mol. Sci. 2013, 14(7), 14974-14995; doi:10.3390/ijms140714974
Abstract: One of the main goals in radiobiology research is to enhance radiotherapy effectiveness without provoking any increase in toxicity. In this context, it has been proposed that electromagnetic fields (EMFs), known to be modulators of proliferation rate, enhancers of apoptosis and inductors of genotoxicity, might control tumor recruitment and, thus, provide therapeutic benefits. Scientific evidence shows that the effects of ionizing radiation on cellular compartments and functions are strengthened by EMF. Although little is known about the potential role of EMFs in radiotherapy (RT), the radiosensitizing effect of EMFs described in the literature could support their use to improve radiation effectiveness. Thus, we hypothesized that EMF exposure might enhance the ionizing radiation effect on tumor cells, improving the effects of RT. The aim of this paper is to review reports of the effects of EMFs in biological systems and their potential therapeutic benefits in radiotherapy.
1. Introduction to Electromagnetic Fields: What They Are and How They Act
Non-ionizing radiation electromagnetic fields (EMFs) is the term that broadly describes the exposures created by the vast array of wired and wireless technologies that have altered the landscape of our lives in countless beneficial ways. Although during recent years, there has been increasing public concern about potential health risks from this non-ionizing subtype of radiation exposure, many people are surprised to learn that certain kinds of EMF treatments can actually heal. Many medical appliances use EMFs in specific ways to help restore bone fractures, to heal wounds to the skin and underlying tissues, to reduce pain and swelling and for other postsurgical needs. In addition, some forms of EMF exposure are used to treat depression . Most electromagnetic medical equipment uses relatively high levels of electric, magnetic or electromagnetic energy .
An electric field (measured in volt/meter (V/m)) exists in a region of space if a charge experiences an electrical force. A magnetic field (MF) (measured in Tesla (T) and the associated magnetic flux density exist only if electric charges are in motion, i.e., if there is a flow of electric current. Electric and magnetic fields are characterized by their magnitude, direction and the frequency characteristics of their sources.
At high frequencies, EMFs propagate by means of tightly coupled electric and magnetic fields (radiation). In radiofrequency fields, tissue penetration ability is frequency-dependent. In the extremely low frequency (ELF) range, electric and magnetic fields are effectively uncoupled and can be evaluated separately as if they arose from independent sources. In this situation, the electric field barely penetrates the body, and the biological effects from ELF fields are due to the action of the unshielded magnetic field.
Depending on their energy, EMFs constitute ionizing radiation when they exert ionizing properties, i.e., when their energy is sufficiently strong to detach electrons from their orbits around atoms and to ionize the atoms as do X-rays or γ-rays. Therefore, long-term exposure to this subtype of radiation results in harmful health effects. However, when their energy is not strong enough to ionize molecules, they are termed non-ionizing EMFs and are considered, at least conceptually, as not harmful. In general, in scientific literature, the term, EMFs, is employed only with respect to the non-ionizing
EMFs located downstream from visible light in the spectrum, and therefore, we will focus on these and use this term (EMFs) to avoid possible confusion. EMFs are traditionally classified according to their oscillatory frequency, as follows: Extremely low frequency (ELF-EMF), low frequency (LF-EMF) and intermediate frequency (IF-EMF), from 0 to 300 kHz, radiofrequency (RF-EMF, 300 kHz–300 MHz) and microwave and radar (MW-EMF, 300 MHz–300 GHz). Tumor-treating electric field (TTField) is a recent term used to describe the alternating electric fields of low intensity (1–3 V/cm) and intermediate frequency (100–300 kHz) that are generated by special insulated electrodes applied to the skin surface.
Biological systems contain EMFs that extend beyond the body. These body-produced EMFs must be distinguished from those produced outside it (i.e., exogenous EMFs). The former are crucial for biological systems, and alterations to them may produce physical and/or behavioral disorders [3,4]. Exogenous EMFs can be divided into two main groups: (1) natural EMFs, including the Earth’s geomagnetic field; and (2) artificial EMFs, including transformers, transmission lines, domestic electric machines, radio transmitters, etc. Natural fields are static or very slowly varying. The electric field in the air above the earth’s surface is typically 100 V/m, but during strong electric storms, it may increase 10-fold or more. The geomagnetic field is typically 50 μT. Obviously, natural EMFs cannot be managed, but artificial ones may be modulated if necessary, for example, when they are associated with risks to human health. Most man-made sources are at extremely low frequencies. The generation, transmission, distribution and use of electricity at 50 or 60 Hz results in the widespread exposure of humans to ELF fields on the order of 10–100 V/m and 0.1–1 μT and, occasionally, to much stronger fields. The term “electronic pollution” has been coined to reflect the fact that exogenous EMFs are probably related to health risk factors . This review addresses EMFs with frequencies ranging from 0.16 Hz to 900 MHz. Although there is some controversy, the majority of data obtained from the studies summarized in this work suggest that the effects of ionizing radiation on cells and tissues are strengthened by EMF, thus supporting its use to improve RT outcome.
Because ELF fields can interact with biological systems, the interest in and concern about potential hazards are understandable. To understand the effects of electric and magnetic fields on humans, their electrical properties, as well as their size and shape have to be considered with respect to the wavelength of the external field. The main difficulty in explaining the effect of electromagnetic radiation on human health resides in our lack of knowledge about the physical-chemical mechanisms underlying life, mainly due to the enormous intrinsic complexity of biological systems. In this respect, Frölich was a pioneer, postulating several years ago that EMFs might exert biological effects, such as coherent electrical polar oscillations, the generation of EMFs in living cells [5–8] and associated disturbances in cancer cells . Since then, many cases of bioelectricity in human beings have been described .
2. Biological Effects of EMFs
The enormous complexity of the molecular mechanisms underlying cell responses to EMF exposure and the lack of consensus regarding treatment schedules are at the heart of the present controversy regarding the biological effects of EMFs (Figure 1). Furthermore, a wide variety of EMFs may be involved, and their consequences may differ widely. In the following paragraphs, we discuss some research findings and attempt to clarify what might take place within the cell after EMF exposure, distinguishing among different EMF treatments (Table 1 summarizes in vitro findings reviewed in this paper and the main characteristic of an applied field).
2.1. Effects on the Cell Membrane
Although there is still no consensus among biophysicians as to whether EMFs traverse the cell membrane, it is generally thought that EMFs have great difficulty in passing through the plasma membrane . Nevertheless, membrane permeability can be transiently increased by applying an electric field, and this impulse might be chemically transmitted. This process has been described in several papers, and many different theories have been postulated about the underlying physical phenomena. Electrical stimulation is known to cause changes in the local pH and/or temperature , and this could lead to membrane destabilization. Intramembrane proteins located in the lipid bilayer, which function as ion channels, may also significantly contribute to this, since EMF exposure leads to the formation of ion channels without cell control, thus inducing severe metabolic modifications . Theoretical models have corroborated this observation, suggesting that a coherent modulation of ion channel gating by an external signal leads to the occurrence of a periodic component in the ion current across a membrane containing a system of multiple channels . This has also been theoretically demonstrated for MW-EMF exposure . We now conduct a brief review of the literature concerning the intracellular alterations observed, preceded or otherwise by membrane alterations, after EMF exposure.
2.2. Effects on the Cell Cytoskeleton
Cell cytoskeleton physiology is responsible for crucial events within the cell, with intracellular transport and cellular division being the most significant of these. In the literature, there is some controversy concerning the influence of EMFs in cytoskeleton physiology. Although some researchers have reported there is no influence of EMFs on the cytoskeleton and/or motor proteins in murine macrophages , many studies have shown that cytoskeleton components are reorganized after exposure to EMFs [13,33]. Kirson et al. suggested that microtubule polymerization may be disrupted by external intermediate-frequency (100–300 kHz), alternating electric fields; likely to influence chromosome alignment and separation. This finding implies that EMFs may affect the generation of mitosis aberrations, leading to mitotic arrest and a decreased rate of proliferation .
2.3. Effects on Cytoplasm
The biological implications of membrane interactions between EMFs and cells are believed to affect the cytoplasm through different cell-signaling pathways. In most cases, the EMF-derived alteration of these pathways would be provoked by the dysregulation of ion channels (as explained above) or by alterations in hormones and second messengers, such as Ca2+ or cyclic adenosine monophosphate (cAMP), although other messengers are also altered by exposure to EMFs .
2.3.1. Disruption of First and Second Messengers
Exactly how MFs disrupt cancer promotion has yet to be established, but the disruption of circulating levels of melatonin has been proposed as a plausible factor in this respect [15,35,36], and recent data indicate that MF exposure also impairs the effects of melatonin within the cell. Melatonin is a lipophilic hormone that can directly cross the membrane and bind to different receptors. In all cases, the melatonin membrane receptors are coupled to second messenger cascades, which vary in cell, tissue and species-specific ways .Thus, many cell features, including cell proliferation, apoptosis and cell cycle progression, are affected by melatonin levels . MF exposure has been reported to impair the effects of melatonin at the cellular level [35,39], although this effect appears to vary according to different experimental conditions.
EMFs can influence the transport of Ca2+ and, hence, its homeostasis [16,17,40]. The processes involved may include the ATPase-dependent Ca2+ pumps present in the endoplasmic reticulum and in the plasma membrane, the Na+/Ca2+electroneutral exchanger and the VOC (voltage-operated calcium channels)-dependent Ca2+ channels . Ca2+ levels may play an important role in modulating cell proliferation, differentiation, apoptosis and cytotoxicity, as well as contributing to the action mechanisms of anticancer agents .
cAMP, a second messenger used for intracellular signal transduction and which conveys the cAMP-dependent pathway, leads a phosphorylation cascade that can activate different pathways. Many researchers have suggested that a deregulation of the cAMP pathways and an aberrant activation of cAMP-controlled genes is linked to apoptosis induction and tumor development inhibition in some cancers [42–44]. ELF-MF treatment has been shown to increase cAMP in a variety of in vitro and in vivo models, including monolayers, spheroids, mice and rats [17,45,46].
2.3.2. Alterations in the MAPK Pathway
It has been suggested that exposure to ELFs-EMFs may affect various cell signaling pathways, including extracellular-regulated kinase (ERK), the 1/2 mitogen-activated protein kinase (MAPK) pathway [18,19,47] and the P38 MAPK pathway [20,47].
MAPKs are a broad family of protein serine/threonine kinases, divided into three major subfamilies. When phosphorylated, the signal is translocated to the nucleus, and gene transcription is activated. We focused on the MAPK pathway, since it is considered the most important one involved in the DNA damage response after ionizing radiation, with the ERK1/2 MAPK subtype being the best-known pathway affected by EMF exposure . Because it is usually modulated by growth factors, but also by cAMP and Ca++ second messengers [21,22], ERK1/2 has been linked to cell proliferation, senescence, differentiation and apoptosis, whereas stress-activated protein kinase/C-Jun N-terminal kinases (SAPK/JNK), another MAPK subtype, has been associated with cell response to inflammation and stress conditions . Jin et al. showed that EMFs are capable of inducing ERK1/2 phosphorylation, whereas the SAPK/JNK pathway is not induced in leukemia and breast cells . Other authors have reported similar results in the same cell lines concerning ERK1/2 and SAPK/JNK activation [47,49]. However, using RF-EMF, both SAPK/JNK and ERK1/2 MAPK subtypes are increased in human neuroblastoma cells . With respect to mobile phone frequencies, Friedman et al. hypothesized that ERK1/2 may be activated by matrix metalloproteinase, released by the EGF (epidermal growth factor), resulting from the generation of reactive oxygen species .
2.4. Nuclear Effects
2.4.1. Gene Expression
Gene expression is meticulously regulated by many pathways. AP-1, a heterodimeric transcription factor composed of proteins belonging to the c-Fos, c-Jun, ATF and JDP families, regulates gene expression in response to a variety of stimuli, controlling a number of cellular processes, including differentiation, proliferation and apoptosis . MFs induce an increased binding activation of AP-1 . Moreover, Jin et al. have demonstrated that AP-1 is induced by EMFs .
RNA binding proteins (RBPs) are another category of cellular regulators of gene expression at the transcriptional level. RBPs usually consist of two subunits, the RNA binding subunit (RBS) and the RNA binding regulatory subunit (RS). Han et al. pointed out that MFs increase RS levels and suggested that RS may also participate in cellular response to MF treatment in the MCF-7 breast cancer cell line .
Furthermore, the activation of the Egr-1 gene may be affected by RF-EMFs together with a significant decrease in mRNA levels of both Bcl-2 and survivin genes .
2.4.2. DNA Damage
Although it is generally accepted that 50/60Hz frequency EMFs might not transfer enough energy to cells to damage DNA directly, certain cellular processes, such as free radicals, may be altered by exposure to EMF, indirectly affecting DNA structure and provoking strand breaks and other chromosomal aberrations, such as micronucleus formation or effects on DNA repair .
220.127.116.11. Oxidative Stress
Oxidative stress, originated by a misbalance between antioxidant molecules (e.g., glutathione, GSH) and reactive oxygen and nitrogen species (ROS and RNS) is crucially involved in carcinogenesis promotion [24,52], due to the resulting genomic instability . Consequently, in vitro studies assessing the role of ROS in biological effects triggered by EMF have been included as a high-priority research line in the World Health Organization Research Agenda (2007).
Rats treated with chronic exposure to RF-EMF have presented decreased antioxidant enzymes, such as superoxide dismutase (SOD) or glutathione peroxidase (GSH-PX), and reduced cellular antioxidant potential . Similar results have been found in rat lymphocytes treated with iron ions  and in rabbits . In addition, a recent paper showed that healthy rats given extremely low frequency EMF treatment also presented increased ROS production, with higher levels of thiobarbituric acid reactive substances (TBARS) and hydrogen peroxide (H2O2) in heart samples after 40 Hz, 7mT, 60 min/day EMF exposure for 14 days. The antioxidant capacity in plasma was also decreased. However, when this treatment schedule was reduced to 30 min/day, no significant decrease in redox status was detected . With respect to cancer research, a number of papers have been published assessing changes in redox status, including neuroblastoma cells , leukemia cells  and fibroblasts [25,26]. In THP-1 acute leukemic cells, EMF reduces antioxidant enzyme activity and enhances nitrogen intermediates involving the iNOS pathway . According to Friedman et al., when HeLa cells are treated with short exposures to RF-EMF, there is an increase in the activity of NADH oxidase, a membrane enzyme, thus inducing ROS production. In consequence, matrix metallo proteinases (MMPs) are synthetized, and these, in turn, release the epidermal growth factor and activate the ERK pathway .
18.104.22.168. Double Strand Breaks, Chromosomal Aberrations and Micronucleus Induction
A survey of the literature suggests that only intermittent EMFs might exert genotoxic cell effects and that cells exposed to continuous EMFs suffer no DNA damage [28,58,59]. In their study of both continuous and intermittent EMF exposures, Ivancstis et al. observed genotoxic effects only when different schedules of intermittent EMFs were used. These authors suggested that subjecting cells to a constant field may induce adaptive mechanisms, protecting the genome from harmful influences, whereas regular changes in environmental conditions might interfere with these mechanisms and lead to DNA impairment in human fibroblasts . Focke et al. extended this study to different human cell models . Kim et al. reported increased levels of γ-H2AX in HeLa and normal lung fibroblasts after daily MF exposure . DNA damage, such as double strand breaks (DSBs) or DNA impairment, leads to genomic instability. In this respect, Winker et al. found that the exposure of cultured human fibroblasts to 50 Hz, 1mT, 15h EMFs resulted in genomic instability marked by increases in chromosomal aberrations . These authors also reported the induction of micronucleus formation after EMF exposure . Micronuclei are cytoplasmic bodies in which part of the acentric chromosome or the whole chromosome is not carried to the opposite pole during anaphase. Their formation has traditionally been associated with genotoxic activity, and micronucleus tests are widely used to evaluate potential carcinogens, since this test has been described as a good biomarker for DNA damage. Micronucleus aberrations could also lead to apoptosis .
2.5. Modulation of Proliferation Rate and Cell Cycle Progression
Cell viability is necessary for a proper response to endogenous factors, such as soluble hormones, growth factors, effectors and genes, and also to exogenous factors, such as cytotoxic drugs and environmental stress . It was recently suggested that repetitive ELF magnetic field exposure with 6 mT decreases cell viability by inducing DNA double strand breaks .
Cell proliferation is a complex process controlled by multiple cell signal transduction pathways. Controversial data have been published concerning the enhancement [31,61], inhibition [62,63] or non-effect of MF exposure with respect to cell proliferation [64,65]. Nevertheless, the scientific contribution of Pasche’s lab seems to be clarifying the potential role of EMFs in proliferation rate control. These authors developed a novel approach to treat advanced hepatocellular carcinoma (HCC), consisting of the intrabuccal administration of very low levels of RF-EMF, amplitude-modulated at specific frequencies in patients with cancer . In a single-group, open-label, phase I/II study consisting of 41 patients with advanced HCC and limited therapeutic options, they observed that treatment with intrabuccally-administered amplitude-modulated electromagnetic fields is safe, well tolerated and shows evidence of antitumor effects in patients with advanced HCC . In a recent in vitro study, the same authors demonstrated that cell proliferation rates in hepatocellular carcinoma and breast cancer cell lines decrease after exposure to EMFs . Focke et al., using fibroblasts , and Kirson et al., using glioma and melanoma cells , also observed a significant inhibition of cell proliferation, suggesting that the optimal frequencies might differ among cancer cell types, being inversely related to cell size [14,69]. Kirson et al. carried out in vivo experiments and found that tumor growth was also decreased in mouse models for both breast and non-small-cell lung carcinomas after exposure to alternating electric fields .
Few studies have been undertaken to assess the role of EMFs in cell cycle progression. Some papers have suggested that there are cell cycle delays in different steps. Kim et al. have reported increased levels of phosphorylated checkpoint kinase 2 (ChK2) after 60Hz ELF-MFs in HeLa and lung fibroblasts , a typical cell cycle checkpoint induced after ionizing radiation-induced DNA damage through the ATM/ATR pathway. Lange et al. found that MFs exerted an inhibitory effect on the G1-phase promotion induced by the altered expression of p16INK4a and p21CIP1. These two proteins are involved in G1 arrest through the destabilization of p53 and the inhibition of cyclinD/Cdk complexes . Since EMF could alter both microtubule polymerization and RBS proteins, thus provoking replication disturbances, it seems reasonable to suggest that EMF exposure may accumulate more cells in the S-phase than in the other cell cycle phases. EMF-exposure causes a significant increase in the percentage of Rat-1 fibroblasts in the S-phase at 12 and 48h, whereas a 30% S-phase decrease has been observed 72 h after EMF exposure, compared to controls . Interestingly, the latter authors also found a significant increase in both DNA strand breaks and 8-OHdG levels, which reached maximum values after the S-phase peaks . RF-EMF treatment has been found to arrest cells in the G2/M phase in human neuroblastoma cells . Using RF-EMF and confocal laser scanning microscopy, Zimmerman et al. found over 60% mitotic spindle disruption in HepG2 cells receiving hepatocellular carcinoma (HCC)-specific RF-EMF, compared with cells not receiving exposure . Nevertheless, Ruiz-Gómez et al. have reported similar cell cycle patterns between unexposed and 25Hz frequency EMF-exposed leukemia and colon carcinoma human cell lines .
2.6. Induced Apoptosis Cascade
MFs affect several important physiological processes related to the mitochondrial membrane potential, such as ATP synthesis, Ca2+ flux and cytochrome c release to the cytosol . Thus, cytochrome c binds to apoptotic protease activating factor-1 (Apaf-1) and ATP to create the apoptosome, capable of triggering apoptosis induction via caspase-9 cleavage . Chromosome and mitotic spindle aberrations also contribute to apoptosis initiation. Therefore, changes in apoptotic rate after EMF exposure could reasonably be expected. Focke et al. reported a slight increase in the percentage of apoptotic fibroblasts after exposure to intermittent EMFs . ELF-EMF also induces apoptosis in tumor cell lines . In most cell types, RF-EMF increases the expression of Egr-1, a strong transcriptional activator of key genes involved in the cell death pathway . Bcl-2 decreases and the apoptosis rate increases after RF-EMF-exposure in human neuroblastoma cells . MW-EMF also induces time-dependent apoptosis in human epidermoid cancer cells .
Evidence is accumulating that components of the plasminogen activator (PA) system are somehow involved in cell death processes. It has been suggested that plasminogen may be linked to apoptosis mediated by cycloheximide (CHX) , dramatically increasing the rate of CHX-induced apoptosis. The latter authors suggest that PA may play a role in the degradative (i.e., late-stage) events of cellular apoptosis . Furthermore, the plasminogen activator system could play an important role in EMF-induced apoptosis through the enhancement of the urokinase plasminogen activator (uPA) . P38 has also been postulated as influential in the induction of apoptosis following EMF exposure. Thus, Kim et al. detected that p38 is only activated upon exposure to a 60 Hz frequency and 6mT MF for 30 min every 24 h for three days. This activation was found after 48 h and 72 h of exposure in HeLa cancer cells and IMP90 lung fibroblasts, respectively. These results suggest that repetitive exposure to a small dose of EMF may induce stress and lead to activation of p38 and other apoptosis-related signaling pathways .
3. EMFs and Magnetic Fields as Useful Adjuvants during Radiotherapy
EMFs are clinically useful in physical medicine to stimulate bone fracture healings , as well as to mitigate chronic pain or edema. However, the biological effects of EMF treatment are not completely elucidated, and there remain possibilities for its inclusion in other medical areas, such as cancer treatment [78,79].
3.1. Genotoxic Effect of Ionizing Radiation
Ionizing electromagnetic radiation is a type of radiation that is frequently used in the treatment of patients with radiotherapy (RT). Typical energies of the photons produced by 4–25 megavolts (MV) are linear accelerators in the RT range from less than 100 kiloelectron volts (keV) to several megaelectron volts (MeV). Although ionizing radiation deposits its energy randomly, causing damage to all molecules, there are multiple copies of most molecules (e.g., mRNA, proteins), which undergo continuous, rapid turnover, thus limiting the consequences of this damage. In contrast, DNA is present in only two copies and has very limited turnover. It is the largest molecule, provides the largest target and is central to all cellular functions. Ionizing radiation can affect DNA directly, generating charged particles or electrons with the kinetic energy of photons (X and γ rays), breaking phosphodiester linkages. This represents around 30% of all DNA damage and is termed the direct action of radiation [80,81]. Other radiation injury is derived from ionizing radiation-raised free radical action and is known as the indirect action of radiation. Briefly, the hydroxyl radical, of considerable biological significance, is formed when ionizing radiation interacts with water molecules, in a process called “water radiolysis”. As a result, free radicals are produced and DNA is harmed. The successful use of radiation to treat cancer results primarily from its ability to cause the death of individual tumor cells, mainly influenced by the amount of DNA damage accumulated, which implies that any agent that increases DNA damage or/and stimulates cell death might potentially improve RT effectiveness.
3.2. In Vitro Effects of EMF and Ionizing Radiation
Although ELF-EMF does not transmit enough energy to affect chemical bonds, it may mediate cell death as a result of the DNA damage induced by oxidative stress, acting as a carcinogen by inducing DNA instability. However, to date, few studies have been performed to assess the potential role of EMFs in RT. In 1999, Miyakoshi et al. suggested that MFs enhance the X-ray mutation rate in ovarian cells . Ding et al. reported similar results in a glioma-derived cell line . Both results might be correlated with DNA instability and, thus, with radiosensitivity. Using a very sensitive method to detect DNA damage involving microsatellite sequences, it has been confirmed that not only is ELF-EMF mutagenic as a single agent, but also that it can potentiate the mutagenicity of ionizing radiation exposure in glioma cells .
Abnormalities in mitotic spindle formation have traditionally been associated with increased apoptosis rates and, thus, with cell radiosensitivity . Therefore, microtubule polymerization disrupted by EMFs may significantly increase apoptosis rates triggered by X-rays. Because it is generally considered that micronuclei containing kinetochore proteins are formed by the lagging of whole chromosomes, the frequency of kinetochore-positive micronuclei can be correlated with genomic instability . The induction of lagging chromosomes has generally been attributed to a dysfunction in the spindle apparatus, such as disruption of the microtubules . Ding et al. reported increased kinetochore-positive micronuclei formation in irradiated cells previously exposed to ELF-MFs compared with non-exposed irradiated cells ; similar results have been reported by Lagroye et al., using EMFs and gamma radiation .
Synergistic effects seem to be the most plausible explanation of the potential role of EMFs during RT. Several studies have investigated the ability of ELFs-MFs to enhance ionizing radiation-induced cytotoxicity and genotoxicity . The existence of cooperative effects between EMFs and X-rays in apoptotic rate induction in a liver cancer cell line has also been demonstrated . An EMF-enhanced key activator of apoptosis cascade, Egr-1, has been postulated as a promising orchestrator between EMFs and ionizing radiation during apoptotic rate induction [19,90,91]. Taking into account that the promoter of Egr-1 contains radiation inducible CArG DNA sequences, consistent results have been developed . Moreover, a radiosensitizer role has been attributed to Egr-1 in melanoma cells , and thus, EMFs could exert a synergistic role in radiosensitivity response. Induced P38 MAPK has also been revealed by repeated exposure to a time-varying magnetic field leading to apoptosis cascade promotion in normal and cancer human cells . Enhanced P38 MAPK activity after ionizing radiation exposure has been reported by many research groups [93–96]. De la Cruz-Morcillo et al. recently reported that ionizing radiation activates p38 MAPK in a p53-dependent fashion, and that activation of the MKK6/3-p38MAPK-p53 signaling axis leads to apoptosis . In addition, an important degree of involvement of p38 MAPK in cell radiosensitivity has been suggested .
Radiosensitivity also depends on the cycle phase of cells during ionizing radiation exposure. It has been shown that cells irradiated during the G2/M-phase are more radiosensitive than when this takes place in other cell cycle phases . Therefore, EMFs causing arrest of the cells in the G2/M-phase might also be useful in radiosensitizing tumor cells [19,31]. P38 MAPK activation has also been related with radiation-induced G2/M arrest . All these results are indicative of synergistic effects by non-ionizing radiation-EMF and ionizing radiation-EMF on the cellular radiosensitive response through p38 activation.
3.3. In Vivo Effects of EMF and Ionizing Radiation
Conceptually, local tumor control is another interesting endpoint for both clinical and experimental research into improving RT effectiveness. A tumor is locally controlled when all of its clonogenic cells (i.e., cells with the capacity to proliferate and to cause recurrence after radiotherapy) have been inactivated . The therapeutic benefit would require a differential effect between tumor cells and normal tissue in order to allow for enhanced radiotherapy effectiveness without increased toxicity. In this sense, Wolf et al.  have demonstrated differences in DNA damage after exposure to ELF-EMFs in both normal and tumor cells. The higher level of DNA damage found in neoplastic cells was associated with defects in repair mechanisms, a common feature of tumor cells. These authors also found that antioxidant treatment (α-tocopherol at 10 μM) prevented stimulation of cell proliferation in normal cells, but not in tumor cells. Differences in DNA damage were also described for normal and tumor cells after this antioxidant treatment. These results show a differential EMF effect between tumor and normal cells. Taking into account the impaired repair capacity of tumor cells, this differential effect could be extended to ionizing radiation treatment, thus supporting the view that the outcome for cells exposed to ionizing radiation could be strengthened by EMF. Experiments carried out on hepatoma-implanted mice have shown that five periods of combined 100 Hz frequency MFs and 4 Gy X-ray could significantly extend the overall days of survival and reduce the tumor size, compared to MF or X-ray treatment alone , suggesting that 100 Hz frequency MF could synergize with X-ray treatment in terms of survival improvement and tumor inhibition in hepatoma-implanted mice. In another study, the combination of EMF and γ-ray exposure produced a synergistic effect by triggering stress response, which increased reactive oxygen species .Cameron et al. reported a synergistic reduction of the growth rate of breast cancer xenografts in EMF/ionizing radiation mice, compared with ionizing radiation therapy . They also reported that the continued daily use of EMFs following a course of ionizing radiation therapy suppressed tumor blood vessel volume density, compared to mice given the ionizing radiation therapy alone. Although ionizing radiation therapy initially interferes with tumor vascularization, leading to tumor hypoxia, which, in turn, enhances the radio-resistance capacity of tumor cells, these hypoxic areas produce HIF-1, leading to the production of angiogenesis growth factors and stimulating further tumor growth. This known sequence of events following ionizing radiation treatment has led researchers to consider ionizing radiation treatment schedules coupled with the use of an anti-angiogenesis agent. Cameron et al. showed that continued daily EMF therapy applied to ionizing radiation-treated mice suppressed the return of blood vessel volume density within the tumor, retarding its vascularization, growth and metastasis .
4. Conclusions and Future Directions
During the last decade, a deep sense of unrest has arisen within society concerning the possibility that human carcinogenesis might be influenced by exposure to extremely low frequency EMFs, now that this type of radiation has become part of everyday life (in diverse areas, from telecommunications to domestic utensils). Recent epidemiological studies have provided evidence of a correlation between chronic exposure to EMFs and an increased incidence of brain, breast and hematological malignancies [100–103]. However, these results are not universally accepted, and the International Agency for Research on Cancer has classified EMF as a 2B carcinogen, taking the view that the epidemiological evidence is “limited” for childhood leukemia and “inadequate” for all other cancers . This classification is also supported by limited evidence in humans and inadequate evidence from experimental animal studies.
In this review, we show that several in vitro studies have explored the potential impact of EMF and ELF magnetic field effects on the membrane structure and permeability of small molecules, such as Ca2+, and on cell proliferation , apoptosis , genotoxicity  and cytoskeleton status . Moreover, these agents have been shown to interfere with chemical reactions involving free radical production, interacting with DNA and hydroxyl radicals, which, in turn, might result in single and double strand breaks [20,60]. Taken together, the data collected in this review seem to indicate that an adjuvant EMF and/or ELFMF treatment enhancing DNA damage may be a plausible means of increasing the ionizing radiation-derived effects on cell and tissues and, thus, increasing RT effectiveness.
Although these studies reflect encouraging results and corroborate the hypothesis that combined exposure to the above agents and ionizing radiation should be used to increase DNA damage, further studies, both in vitro and in vivo, should be conducted to validate the effectiveness and therapeutic benefits of this use of radiosensitizing agents in cancer RT. Moreover, the findings presented in this paper imply that the cellular response to EMF and/or ELF MFs is highly variable among cell lines and/or specimens, affecting certain cell types, in particular. Thus, further evaluation is required to determine their possible clinical relevance, especially in combination with RT.
This study was supported by the Instituto de Salud Carlos III, Fondo de Investigación Sanitaria (PI08/0728, Fondos FEDER) to M.I. Núñez. F. Artacho-Cordón is supported by the Spanish Ministry of Science and Education (AP2012-2524). A grant from the Fundación Benéfica San Francisco Javier y Santa Cándida, University of Granada, to S. Ríos-Arrabal greatly aided this work. This research was also funded by the San Cecilio University Hospital, Granada. The authors thank Glenn Harding for improving the English style of the manuscript.
Conflict of Interest
The authors declare that they have no competing interests.
- Malmivuo, J.; Plonsey, R. Bioelectromagnetism: Principles and Applications of Bioelectric and Biomagnetic Fields; Oxford University Press: New York, NY, USA, 1995. [Google Scholar]
- IARC Working Group on the Evalutation of Carcinogenic Risks to Humans. Non-ionizing radiation, part 1: Static and extremely low-frequency (ELF) electric and magnetic fields. IARC Monogr. Eval. Carcinog. Risks to Hum. 2002, 80, 1–395.
- Schreier, N.; Huss, A.; Röösli, M. The prevalence of symptoms attributed to electromagnetic field exposure: A cross-sectional representative survey in Switzerland. Soc. Prev. Med 2006, 51, 202–209. [Google Scholar]
- Rubin, G.J.; Nieto-Hernandez, R.; Wessely, S. Idiopathic environmental intolerance attributed to electromagnetic fields (formerly “electromagnetic hypersensitivity”): An updated systematic review of provocation studies. Bioelectromagnetics 2010, 31, 1–11. [Google Scholar]
- Fröhlich, H. Bose condensation of strongly excited longitudinal electric modes. Phys. Lett. A 1968, 26, 402–403. [Google Scholar]
- Fröhlich, H. Quantum mechanical concepts in biology. Theoret. Phys. Biol 1969, 1, 13–22. [Google Scholar]
- Fröhlich, H. Long-range coherence and energy storage in biological systems. Int. J. Quantum Chem 1968, 2, 641–649. [Google Scholar]
- Fröhlich, H. Collective behaviour of non-linearly coupled oscillating fields (with applications to biological systems). J. Collect. Phenom 1973, 1, 101. [Google Scholar]
- Frohlich, H. Coherent electric vibrations in biological systems and the cancer problem. IEEE Trans. Microw. Theory Tech 1978, 26, 613–618. [Google Scholar]
- Funk, R.H.; Monsees, T.; Özkucur, N. Electromagnetic effects—From cell biology to medicine. Prog. Histochem. Cytochem 2009, 43, 177–264. [Google Scholar]
- Galvanovskis, J.; Sandblom, J. Amplification of electromagnetic signals by ion channels. Biophys. J 1997, 73, 3056–3065. [Google Scholar]
- Cagni, E.; Remondini, D.; Mesirca, P.; Castellani, G.C.; Verondini, E.; Bersani, F. Effects of exogenous electromagnetic fields on a simplified ion channel model. J. Biol. Phys 2007, 33, 183–194. [Google Scholar]
- Pokorny, J. Physical aspects of biological activity and cancer. AIP Adv. 2012, 2. [Google Scholar] [CrossRef]
- Kirson, E.D.; Gurvich, Z.; Schneiderman, R.; Dekel, E.; Itzhaki, A.; Wasserman, Y.; Schatzberger, R.; Palti, Y. Disruption of cancer cell replication by alternating electric fields. Cancer Res 2004, 64, 3288–3295. [Google Scholar]
- Touitou, Y.; Bogdan, A.; Lambrozo, J.; Selmaoui, B. Is melatonin the hormonal missing link between magnetic field effects and human diseases? Cancer Causes Control 2006, 17, 547–552. [Google Scholar]
- Strauch, B.; Herman, C.; Dabb, R.; Ignarro, L.J.; Pilla, A.A. Evidence-based use of pulsed electromagnetic field therapy in clinical plastic surgery. Aesthet. Surg. J 2009, 29, 135–143. [Google Scholar]
- Manikonda, P.K.; Rajendra, P.; Devendranath, D.; Gunasekaran, B.; Channakeshava Aradhya, R.S.S.; Sashidhar, R.B.; Subramanyam, C. Influence of extremely low frequency magnetic fields on Ca2+ signaling and nmda receptor functions in rat hippocampus. Neurosci. Lett. 2007, 413, 145–149. [Google Scholar]
- Jin, M.; Blank, M.; Goodman, R. Erk1/2 phosphorylation, induced by electromagnetic fields, diminishes during neoplastic transformation. J. Cell. Biochem 2000, 78, 371–379. [Google Scholar]
- Buttiglione, M.; Roca, L.; Montemurno, E.; Vitiello, F.; Capozzi, V.; Cibelli, G. Radiofrequency radiation (900 MHz) induces Egr-1 gene expression and affects cell-cycle control in human neuroblastoma cells. J. Cell. Physiol 2007, 213, 759–767. [Google Scholar]
- Kim, J.; Ha, C.S.; Lee, H.J.; Song, K. Repetitive exposure to a 60-Hz time-varying magnetic field induces DNA double-strand breaks and apoptosis in human cells. Biochem. Biophys. Res. Commun 2010, 400, 739–744. [Google Scholar]
- Busca, R.; Abbe, P.; Mantoux, F.; Aberdam, E.; Peyssonnaux, C.; Eychene, A.; Ortonne, J.-P.; Ballotti, R. Ras mediates the cAMP-dependent activation of extracellular signal-regulated kinases (ERKs) in melanocytes. EMBO J 2000, 19, 2900–2910. [Google Scholar]
- Yamaguchi, T.; Wallace, D.P.; Magenheimer, B.S.; Hempson, S.J.; Grantham, J.J.; Calvet, J.P. Calcium restriction allows camp activation of the b-raf/erk pathway, switching cells to a cAMP-dependent growth-stimulated phenotype. J. Biol. Chem 2004, 279, 40419–40430. [Google Scholar]
- Ruiz-Gómez, M.J.; Martínez-Morillo, M. Electromagnetic fields and the induction of DNA strand breaks. Electromagn. Biol. Med 2009, 28, 201–214. [Google Scholar]
- Anastassopoulou, J.; Theophanides, T. Magnesium-DNA interactions and the possible relation of magnesium to carcinogenesis. Irradiation and free radicals. Crit. Rev. Oncol. Hematol 2002, 42, 79–91. [Google Scholar]
- Lee, H.J.; Jin, Y.B.; Lee, J.S.; Choi, J.I.; Lee, J.W.; Myung, S.H.; Lee, Y.S. Combined effects of 60 Hz electromagnetic field exposure with various stress factors on cellular transformation in NIH3T3 cells. Bioelectromagnetics 2011, 33, 207–214. [Google Scholar]
- Jin, Y.B.; Kang, G.-Y.; Lee, J.S.; Choi, J.-I.; Lee, J.-W.; Hong, S.-C.; Myung, S.H.; Lee, Y.-S. Effects on micronuclei formation of 60-Hz electromagnetic field exposure with ionizing radiation, hydrogen peroxide, or c-Myc overexpression. Int. J. Radiat. Biol 2012, 88, 374–380. [Google Scholar]
- Goraca, A.; Ciejka, E.; Piechota, A. Effects of extremely low frequency magnetic field on the parameters of oxidative stress in heart. J. Physiol. Pharmacol 2010, 61, 333–338. [Google Scholar]
- Falone, S.; Grossi, M.R.; Cinque, B.; D’Angelo, B.; Tettamanti, E.; Cimini, A.; di Ilio, C.; Amicarelli, F. Fifty hertz extremely low-frequency electromagnetic field causes changes in redox and differentiative status in neuroblastoma cells. Int. J. Biochem. Cell Biol 2007, 39, 2093–2106. [Google Scholar]
- Focke, F.; Schuermann, D.; Kuster, N.; Schär, P. DNA fragmentation in human fibroblasts under extremely low frequency electromagnetic field exposure. Mutat. Res. Fundam. Mol. Mech. Mutagenes 2010, 683, 74–83. [Google Scholar]
- Hynes, J.; Floyd, S.; Soini, A.E.; O’Connor, R.; Papkovsky, D.B. Fluorescence-based cell viability screening assays using water-soluble oxygen probes. J. Biomol. Screen 2003, 8, 264–272. [Google Scholar]
- Wolf, F.I.; Torsello, A.; Tedesco, B.; Fasanella, S.; Boninsegna, A.; D’Ascenzo, M.; Grassi, C.; Azzena, G.B.; Cittadini, A. 50-Hz extremely low frequency electromagnetic fields enhance cell proliferation and DNA damage: Possible involvement of a redox mechanism. BBA Mol. Cell Res 2005, 1743, 120–129. [Google Scholar]
- Simkó, M.; Droste, S.; Kriehuber, R.; Weiss, D.G. Stimulation of phagocytosis and free radical production in murine macrophages by 50 Hz electromagnetic fields. Eur. J. Cell Biol 2001, 80, 562–566. [Google Scholar]
- Santoro, N.; Lisi, A.; Pozzi, D.; Pasquali, E.; Serafino, A.; Grimaldi, S. Effect of extremely low frequency (ELF) magnetic field exposure on morphological and biophysical properties of human lymphoid cell line (RAJI). BBA Mol. Cell Res 1997, 1357, 281–290. [Google Scholar]
- Pilla, A.; Fitzsimmons, R.; Muehsam, D.; Wu, J.; Rohde, C.; Casper, D. Electromagnetic fields as first messenger in biological signaling: Application to calmodulin-dependent signaling in tissue repair. BBA Gen. Subj 2011, 1810, 1236–1245. [Google Scholar]
- Löscher, W.; Mevissen, M. Animal studies on the role of 50/60-Hertz magnetic fields in carcinogenesis. Life Sci 1994, 54, 1531–1543. [Google Scholar]
- Touitou, Y.; Lambrozo, J.; Camus, F.; Charbuy, H. Magnetic fields and the melatonin hypothesis: A study of workers chronically exposed to 50-Hz magnetic fields. Am. J. Physiol. Regul. Integr. Comp. Physiol 2003, 284, R1529–R1535. [Google Scholar]
- Luchetti, F.; Canonico, B.; Betti, M.; Arcangeletti, M.; Pilolli, F.; Piroddi, M.; Canesi, L.; Papa, S.; Galli, F. Melatonin signaling and cell protection function. FASEB J 2010, 24, 3603–3624. [Google Scholar]
- Mediavilla, M.D.; Sanchez-Barcelo, E.J.; Tan, D.X.; Manchester, L.; Reiter, R.J. Basic mechanisms involved in the anti-cancer effects of melatonin. Curr. Med. Chem 2010, 17, 4462–4481. [Google Scholar]
- Liburdy, R.P.; Sloma, T.R.; Sokolic, R.; Yaswen, P. ELF magnetic fields, breast cancer, and melatonin: 60 Hz fields block melatonin’s oncostatic action on ER+ breast cancer cell proliferation. J. Pineal Res 1993, 14, 89–97. [Google Scholar]
- Aldinucci, C.; Palmi, M.; Sgaragli, G.; Benocci, A.; Meini, A.; Pessina, F.; Pessina, G.P. The effect of pulsed electromagnetic fields on the physiologic behaviour of a human astrocytoma cell line. BBA Mol. Cell Res 2000, 1499, 101–108. [Google Scholar]
- Sergeev, I.; Rhoten, W. Regulation of intracellular calcium in human breast cancer cells. Endocrine 1998, 9, 321–327. [Google Scholar]
- Follin-Arbelet, V.; Hofgaard, P.; Hauglin, H.; Naderi, S.; Sundan, A.; Blomhoff, R.; Bogen, B.; Blomhoff, H. Cyclic AMP induces apoptosis in multiple myeloma cells and inhibits tumor development in a mouse myeloma model. BMC Cancer 2011, 11. [Google Scholar] [CrossRef]
- Rocha, A.S.; Paternot, S.; Coulonval, K.; Dumont, J.E.; Soares, P.; Roger, P.P. Cyclic AMP inhibits the proliferation of thyroid carcinoma cell lines through regulation of cdk4 phosphorylation. Mol. Biol. Cell 2008, 19, 4814–4825. [Google Scholar]
- Dumaz, N.; Light, Y.; Marais, R. Cyclic AMP blocks cell growth through Raf-1-dependent and Raf-1-independent mechanisms. Mol. Cell. Biol 2002, 22, 3717–3728. [Google Scholar]
- Schimmelpfeng, J.; Stein, J.-C.; Dertinger, H. Action of 50 Hz magnetic fields on cyclic AMP and intercellular communication in monolayers and spheroids of mammalian cells. Bioelectromagnetics 1995, 16, 381–386. [Google Scholar]
- Hogan, M.V.; Wieraszko, A. An increase in cAMP concentration in mouse hippocampal slices exposed to low-frequency and pulsed magnetic fields. Neurosci. Lett 2004, 366, 43–47. [Google Scholar]
- Friedman, J.; Kraus, S.; Hauptman, Y.; Schiff, Y.; Seger, R. Mechanism of short-term ERK activation by electromagnetic fields at mobile phone frequencies. Biochem. J. 2007, 405. [Google Scholar] [CrossRef]
- Dent, P.; Yacoub, A.; Fisher, P.B.; Hagan, M.P.; Grant, S. MAPK pathways in radiation responses. Oncogene 2003, 22, 5885–5896. [Google Scholar]
- Nie, K.; Henderson, A. MAP kinase activation in cells exposed to a 60 Hz electromagnetic field. J. Cell. Biochem 2003, 90, 1197–1206. [Google Scholar]
- Lin, H.; Han, L.; Blank, M.; Head, M.; Goodman, R. Magnetic field activation of protein-DNA binding. J. Cell. Biochem 1998, 70, 297–303. [Google Scholar]
- Li, H.; Zeng, Q.; Weng, Y.; Lu, D.; Jiang, H.; Xu, Z. Effects of elf magnetic fields on protein expression profile of human breast cancer cell MCF7. Sci. China Ser. C 2005, 48, 506–514. [Google Scholar]
- Marnett, L.J. Oxyradicals and DNA damage. Carcinogenesis 2000, 21, 361–370. [Google Scholar]
- Colotta, F.; Allavena, P.; Sica, A.; Garlanda, C.; Mantovani, A. Cancer-related inflammation, the seventh hallmark of cancer: Links to genetic instability. Carcinogenesis 2009, 30, 1073–1081. [Google Scholar]
- Desai, N.; Kesari, K.; Agarwal, A. Pathophysiology of cell phone radiation: Oxidative stress and carcinogenesis with focus on male reproductive system. Reprod. Biol. Endocrinol. 2009, 7. [Google Scholar] [CrossRef]
- Zmyślony, M.; Politanski, P.; Rajkowska, E.; Szymczak, W.; Jajte, J. Acute exposure to 930 MHz CW electromagnetic radiation in vitro affects reactive oxygen species level in rat lymphocytes treated by iron ions. Bioelectromagnetics 2004, 25, 324–328. [Google Scholar]
- Irmak, M.K.; Fadıllıoğlu, E.; Güleç, M.; Erdoğan, H.; Yağmurca, M.; Akyol, Ö. Effects of electromagnetic radiation from a cellular telephone on the oxidant and antioxidant levels in rabbits. Cell Biochem. Funct. 2002, 20, 279–283. [Google Scholar]
- Patruno, A.; Pesce, M.; Marrone, A.; Speranza, L.; Grilli, A.; de Lutiis, M.A.; Felaco, M.; Reale, M. Activity of matrix metallo proteinases (MMPs) and the tissue inhibitor of MMP (TIMP)-1 in electromagnetic field-exposed THP-1 cells. J. Cell. Physiol 2012, 227, 2767–2774. [Google Scholar]
- Hintzsche, H.; Jastrow, C.; Kleine-Ostmann, T.; Kärst, U.; Schrader, T.; Stopper, H. Terahertz electromagnetic fields (0.106 THz) do not induce manifest genomic damage in vitro. PloS One 2012, 7. [Google Scholar] [CrossRef]
- Winker, R.; Ivancsits, S.; Pilger, A.; Adlkofer, F.; Rüdiger, H. Chromosomal damage in human diploid fibroblasts by intermittent exposure to extremely low-frequency electromagnetic fields. Mutat. Res. Genet. Toxicol. Environ. Mutagenes 2005, 585, 43–49. [Google Scholar]
- Ivancsits, S.; Diem, E.; Pilger, A.; Rudiger, H.W.; Jahn, O. Induction of DNA strand breaks by intermittent exposure to extremely-low-frequency electromagnetic fields in human diploid fibroblasts. Mutat. Res. Genet. Toxicol. Environ. Mutagenes 2002, 519, 1–13. [Google Scholar]
- Ruiz-Gómez, M.J.; Sendra-Portero, F.; Martínez-Morillo, M. Effect of 2.45 mT sinusoidal 50 Hz magnetic field on Saccharomyces cerevisiae strains deficient in DNA strand breaks repair. Int. J. Radiat. Biol 2010, 86, 602–611. [Google Scholar]
- Tofani, S.; Barone, D.; Cintorino, M.; de Santi, M.M.; Ferrara, A.; Orlassino, R.; Ossola, P.; Peroglio, F.; Rolfo, K.; Ronchetto, F. Static and ELF magnetic fields induce tumor growth inhibition and apoptosis. Bioelectromagnetics 2001, 22, 419–428. [Google Scholar]
- Tatarov, I.; Panda, A.; Petkov, D.; Kolappaswamy, K.; Thompson, K.; Kavirayani, A.; Lipsky, M.M.; Elson, E.; Davis, C.C.; Martin, S.S. Effect of magnetic fields on tumor growth and viability. Comp. Med 2011, 61, 339–345. [Google Scholar]
- Yoshizawa, H.; Tsuchiya, T.; Mizoe, H.; Ozeki, H.; Kanao, S.; Yomori, H.; Sakane, C.; Hasebe, S.; Motomura, T.; Yamakawa, T. No effect of extremely low-frequency magnetic field observed on cell growth or initial response of cell proliferation in human cancer cell lines. Bioelectromagnetics 2002, 23, 355–368. [Google Scholar]
- Ruiz-Gómez, M.J.; Prieto-Barcia, M.I.; Ristori-Bogajo, E.; Martínez-Morillo, M. Static and 50 Hz magnetic fields of 0.35 and 2.45 mT have no effect on the growth of saccharomyces cerevisiae. Bioelectrochemistry 2004, 64, 151–155. [Google Scholar]
- Alexandre, B.; Frederico, C.; Brad, B.; Reginald, M.; Fin, B.; Niels, K.; Boris, P. Amplitude-modulated electromagnetic fields for the treatment of cancer: Discovery of tumor-specific frequencies and assessment of a novel therapeutic approach. J. Exp. Clin. Cancer Res. 2009, 28. [Google Scholar] [CrossRef]
- Costa, F.; de Oliveira, A.; Meirelles, R.; Machado, M.; Zanesco, T.; Surjan, R.; Chammas, M.; de Souza Rocha, M.; Morgan, D.; Cantor, A. Treatment of advanced hepatocellular carcinoma with very low levels of amplitude-modulated electromagnetic fields. Br. J. Cancer 2011, 105, 640–648. [Google Scholar]
- Zimmerman, J.; Pennison, M.; Brezovich, I.; Yi, N.; Yang, C.; Ramaker, R.; Absher, D.; Myers, R.; Kuster, N.; Costa, F. Cancer cell proliferation is inhibited by specific modulation frequencies. Br. J. Cancer 2011, 106, 307–313. [Google Scholar]
- Kirson, E.D.; Dbalý, V.; Tovaryš, F.; Vymazal, J.; Soustiel, J.F.; Itzhaki, A.; Mordechovich, D.; Steinberg-Shapira, S.; Gurvich, Z.; Schneiderman, R. Alternating electric fields arrest cell proliferation in animal tumor models and human brain tumors. Proc. Natl. Acad. Sci. USA 2007, 104, 10152–10157. [Google Scholar]
- Lange, S.; Richard, D.; Viergutz, T.; Kriehuber, R.; Weiss, D.G.; Simkó, M. Alterations in the cell cycle and in the protein level of cyclin D1, p21CIP1, and p16INK4a after exposure to 50 Hz MF in human cells. Radiat. Environ. Biophys 2002, 41, 131–137. [Google Scholar]
- Ruiz Gómez, M.J.; de la Peña, L.; Pastor, J.M.; Martínez Morillo, M.; Gil, L. 25 Hz electromagnetic field exposure has no effect on cell cycle distribution and apoptosis in U-937 and HCA-2/1cch cells. Bioelectrochemistry 2001, 53, 137–140. [Google Scholar]
- Gorczynska, E.; Wegrzynowicz, R. Structural and functional changes in organelles of liver cells in rats exposed to magnetic fields. Environ. Res 1991, 55, 188–198. [Google Scholar]
- Reubold, T.F.; Eschenburg, S. A molecular view on signal transduction by the apoptosome. Cell. Signal 2012, 24, 1420–1425. [Google Scholar]
- Caraglia, M.; Marra, M.; Mancinelli, F.; D’ambrosio, G.; Massa, R.; Giordano, A.; Budillon, A.; Abbruzzese, A.; Bismuto, E. Electromagnetic fields at mobile phone frequency induce apoptosis and inactivation of the multi-chaperone complex in human epidermoid cancer cells. J. Cell. Physiol 2005, 204, 539–548. [Google Scholar]
- O’Mullane, M.J.; Baker, M.S. Elevated plasminogen receptor expression occurs as a degradative phase event in cellular apoptosis. Immunol. Cell Biol 1999, 77, 249–255. [Google Scholar]
- Girgert, R.; Emons, G.; Hanf, V.; Gründker, C. Exposure of MCF-7 breast cancer cells to electromagnetic fields up-regulates the plasminogen activator system. Int. J. Gynecol. Cancer 2009, 19, 334–338. [Google Scholar]
- Kovacic, P.; Somanathan, R. Electromagnetic fields: Mechanism, cell signaling, other bioprocesses, toxicity, radicals, antioxidants and beneficial effects. J. Recept. Signal Transduct 2010, 30, 214–226. [Google Scholar]
- Cameron, I.L.; Sun, L.Z.; Short, N.; Hardman, W.E.; Williams, C.D. Therapeutic electromagnetic field (TEMF) and gamma irradiation on human breast cancer xenograft growth, angiogenesis and metastasis. Cancer Cell Int. 2005, 5. [Google Scholar] [CrossRef]
- Wen, J.; Jiang, S.; Chen, B. The effect of 100 Hz magnetic field combined with X-ray on hepatoma-implanted mice. Bioelectromagnetics 2011, 32, 322–324. [Google Scholar]
- Jeggo, P.A. Risks from low dose/dose rate radiation: What an understanding of DNA damage response mechanisms can tell us. Health Phys 2009, 97, 416–425. [Google Scholar]
- Kempner, E.S. Molecular size determination of enzymes by radiation inactivation. Adv. Enzymol. Relat. Areas Mol. Biol. 1988, 107–147. [Google Scholar]
- Miyakoshi, J.; Koji, Y.; Wakasa, T.; Takebe, H. Long-term exposure to a magnetic field (5 mT at 60 Hz) increases X-ray-induced mutations. J. Radiat. Res 1999, 40, 13–21. [Google Scholar]
- Ding, G.-R.; Yaguchi, H.; Yoshida, M.; Miyakoshi, J. Increase in X-ray-induced mutations by exposure to magnetic field (60 hz, 5 mt) in nf-κb-inhibited cells. Biochem. Biophys. Res. Commun 2000, 276, 238–243. [Google Scholar]
- Mairs, R.J.; Hughes, K.; Fitzsimmons, S.; Prise, K.M.; Livingstone, A.; Wilson, L.; Baig, N.; Clark, A.M.; Timpson, A.; Patel, G.; et al. Microsatellite analysis for determination of the mutagenicity of extremely low-frequency electromagnetic fields and ionising radiation in vitro. Mutat. Res. Genet. Toxicol. Environ. Mutagenes 2007, 626, 34–41. [Google Scholar]
- Joiner, M.; van der Kogel, A. Basic Clinical Radiobiology, 4th ed; Hodder Arnold: London, UK, 2009; Volume 1, pp. 41–55. [Google Scholar]
- Ding, G.R.; Nakahara, T.; Miyakoshi, J. Induction of kinetochore-positive and kinetochore-negative micronuclei in CHO cells by ELF magnetic fields and/or X-rays. Mutagenesis 2003, 18, 439–443. [Google Scholar]
- Lagroye, I.; Poncy, J.L. The effect of 50 Hz electromagnetic fields on the formation of micronuclei in rodent cell lines exposed to gamma radiation. Int. J. Radiat. Biol 1997, 72, 249–254. [Google Scholar]
- Manti, L.; D’Arco, A. Cooperative biological effects between ionizing radiation and other physical and chemical agents. Mutat. Res. Rev. Mutat. Res 2010, 704, 115–122. [Google Scholar]
- Jian, W.; Wei, Z.; Zhiqiang, C.; Zheng, F. X-ray-induced apoptosis of BEL-7402 cell line enhanced by extremely low frequency electromagnetic field in vitro. Bioelectromagnetics 2009, 30, 163–165. [Google Scholar]
- Ahmed, M.M.; Sells, S.F.; Venkatasubbarao, K.; Fruitwala, S.M.; Muthukkumar, S.; Harp, C.; Mohiuddin, M.; Rangnekar, V.M. Ionizing radiation-inducible apoptosis in the absence of p53 linked to transcription factor EGR-1. J. Biol. Chem 1997, 272, 33056–33061. [Google Scholar]
- Ahmed, M.M. Regulation of radiation-induced apoptosis by early growth response-1 gene in solid tumors. Curr. Cancer Drug Targets 2004, 4, 43–52. [Google Scholar]
- Ahmed, M.M.; Venkatasubbarao, K.; Fruitwala, S.M.; Muthukkumar, S.; Wood, D.P., Jr; Sells, S.F.; Mohiuddin, M.; Rangnekar, V.M. EGR-1 induction is required for maximal radiosensitivity in A375-C6 melanoma cells. J. Biol. Chem. 1996, 271, 29231–29237. [Google Scholar]
- Wang, Y.; Liu, L.; Zhou, D. Inhibition of p38 MAPK attenuates ionizing radiation-induced hematopoietic cell senescence and residual bone marrow injury. Radiat. Res 2011, 176, 743–752. [Google Scholar]
- De la Cruz-Morcillo, M.; Valero, M.; Callejas-Valera, J.; Arias-Gonzalez, L.; Melgar-Rojas, P.; Galán-Moya, E.; García-Gil, E.; García-Cano, J.; Sánchez-Prieto, R. P38MAPK is a major determinant of the balance between apoptosis and autophagy triggered by 5-fluorouracil: Implication in resistance. Oncogene 2011, 31, 1073–1085. [Google Scholar]
- Dickinson, S.E.; Olson, E.R.; Zhang, J.; Cooper, S.J.; Melton, T.; Criswell, P.J.; Casanova, A.; Dong, Z.; Hu, C.; Saboda, K. P38 MAP kinase plays a functional role in UVB-induced mouse skin carcinogenesis. Mol. Carcinogenes 2011, 50, 469–478. [Google Scholar]
- Wood, C.D.; Thornton, T.M.; Sabio, G.; Davis, R.A.; Rincon, M. Nuclear localization of p38 MAPK in response to DNA damage. Int. J. Biol. Sci 2009, 5, 428–437. [Google Scholar]
- De la Cruz-Morcillo, M.A.; García-Cano, J.; Arias-González, L.; García-Gil, E.; Artacho-Cordón, F.; Ríos-Arrabal, S.; Valero, M.L.; Cimas, F.J.; Serrano-Oviedo, L.; Villas, M.V. Abrogation of the p38 MAPKα signaling pathway does not promote radioresistance but its activity is required for 5-fluorouracil-associated radiosensitivity. Cancer Lett 2013, 335, 66–74. [Google Scholar]
- Wang, X.; McGowan, C.H.; Zhao, M.; He, L.; Downey, J.S.; Fearns, C.; Wang, Y.; Huang, S.; Han, J. Involvement of the MKK6-p38γ cascade in γ-radiation-induced cell cycle arrest. Mol. Cell. Biol 2000, 20, 4543–4552. [Google Scholar]
- Cao, Y.; Zhang, W.; Lu, M.X.; Xu, Q.; Meng, Q.Q.; Nie, J.H.; Tong, J. 900-MHz microwave radiation enhances γ-ray adverse effects on SHG44 cells. J. Toxicol. Environ. Health A 2009, 72, 727–732. [Google Scholar]
- Baan, R.; Grosse, Y.; Lauby-Secretan, B.; El Ghissassi, F.; Bouvard, V.; Benbrahim-Tallaa, L.; Guha, N.; Islami, F.; Galichet, L.; Straif, K. Carcinogenicity of radiofrequency electromagnetic fields. Lancet Oncol 2011, 12, 624–626. [Google Scholar]
- Ahlbom, I.; Cardis, E.; Green, A.; Linet, M.; Savitz, D.; Swerdlow, A. Review of the epidemiologic literature on EMF and health. Environ. Health Perspect 2001, 109, 911–933. [Google Scholar]
- Calvente, I.; Fernandez, M.; Villalba, J.; Olea, N.; Nuñez, M. Exposure to electromagnetic fields (non-ionizing radiation) and its relationship with childhood leukemia: A systematic review. Sci. Total Environ 2010, 408, 3062–3069. [Google Scholar]
- Linet, M.S.; Hatch, E.E.; Kleinerman, R.A.; Robison, L.L.; Kaune, W.T.; Friedman, D.R.; Severson, R.K.; Haines, C.M.; Hartsock, C.T.; Niwa, S. Residential exposure to magnetic fields and acute lymphoblastic leukemia in children. N. Engl. J. Med 1997, 337, 1–8. [Google Scholar]
|Cell compartment||Frequency||Intensity||Time||EMF type||Biological effect||Reference|
|Cell membrane||25 pulses/s||Peak: 0.25 T; Average: 0.5 T||238 μs 1000 pulses/day||AC MF||Changes in the local pH and/or temperature|||
|<100 Hz||<100 μT||0–8 ns||MF||Formation of ion channels|||
|MW (≈1 GHz)||>105 V/m||Several periods of oscillation||EF|||
|Cell cytoskeleton||50 Hz||0.5–1.5 mT||45 min||MF||No influence of EMF on cytoskeleton and/or motor proteins|||
|50 Hz||2 mT (rms)||72 h||MF||Changes in microtubule polymerization|||
|100–300 kHz||2 V/cm||24 h||AC EF|||
|1st/2nd messengers||60 Hz||1.9–11.95 mG||–||MF||Melatonin involved in transmission of EMF into the cell|||
|50 Hz||Peak: 3 mT||24 h||EMF||Influence the transport of Ca2+ and, hence, its homeostasis|||
|50 Hz||2 mT||5 min||MF||Deregulation of the cAMP concentration|||
|MAPK pathway||60Hz||0.8–300 μT||30 min||EMF||Induction of ERK1/2 phosphorylation|||
|875 MHz||0.005, 0.03 and 0.11 mW/cm2||30 min||EMF (S)|||
|900 MHz||1 W/kg||24 h||EMF (SAR)|||
|875 MHz||0.10 mW/cm2||30 min||EMF (S)||P38 MAPK activation|||
|60 Hz||6 mT||30 min/day;3 days||AC MF|||
|Gene expression||60 Hz||0.8–300 μT||60 min||MF||Increase of AP-1 transcription factor|||
|60 Hz||8 μT||20 min field-on; 20 min field-off|||
|50 Hz||0.4 mT||20 min||MF||Increase RNA binding protein levels|||
|900 MHz||1 W/kg||–||EMF (SAR)||Increase in mRNA levels of Egr-1, Bcl-2 and survivin genes|||
|1. Oxidative stress|
|1.1. Antioxidant system||50 Hz||1 mT rms||24 h||AC MF||↓ SOD activity|||
|50 Hz||1 mT||<96 h||MF||= SOD activity|||
|50 Hz||1 mT rms||24 h||AC MF||↓ Catalase activity|||
|50 Hz||1 mT||<96h||MF||Glutathione S-transferase|||
|50 Hz||1 mT||<96h||MF||Glutathione peroxidase|||
|50 Hz||1 mT||<96h||MF||↑ Reduced/total GSH ratio|||
|1.2. Pro-oxidant molecules||50 Hz||1 mT rms||24 h||MF||↑ iNOS|||
|930 MHz||5 W/m2||5–15 min||CW EMF (S)||↑ ROS|||
|900 MHz||2 W peak 0.02 mW/cm2||30 min/day; 7 days||EMF (S)|||
|50 Hz||1 mT rms||24 h||AC MF|||
|50 Hz||1 mT||<96 h||MF||= ROS|||
|2. Genotoxicity||60 Hz||6 mT||30 min/day; 1–3 days||AC MF||Increased levels of γH2AX|||
|50 Hz||1 mT||15 h, 5 field-on/10 field-off||MF||Double Strand Breaks|||
|50 Hz||1 mT||24 h||MF|||
|50 Hz||1 mT||15 h||EMF|||
|50 Hz||1 mT||15 h, 5′ field-on/10′ field-off||MF||Chromosome aberrations|||
|50 Hz||1 mT||2–24 h, 5′ field-on/10′ field-off.||MF||Micronucleus induction|||
AC: alternating current;cAMP:adenosine monophosphate; CW: continuous wave;DSBs: double strand breaks; EF: electric fields; EMF: electromagnetic fields; GSH: reduced glutathione; iNOS: inducible nitric oxide synthetase; MF: magnetic field; MW: microwave; rms: root mean square; S: power density, SAR: absorption rate; ROS: reactive oxygen species; SOD: superoxide dismutase.
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