Favourable and Unfavourable EMF Frequency Patterns in Cancer : Perspectives for Improved Therapy and Prevention

Carcinogenesis fits in a frequency pattern of electromagnetic field (EMF) waves, in which a gradual loss of cellular organization occurs. Such generation of cancer features can be inhibited by adequate exposure to coherent electromagnetic frequencies. However, cancer can also be initiated and promoted at other distinct frequencies of electromagnetic waves. Both observations were revealed by analyzing 100 different EMF frequency data reported in a meta-analyses of 123 different, earlier published, biomedical studies. The studied EM frequencies showed a fractal pattern of 12 beneficial (anti-cancer) frequencies, and 12 detrimental (cancer promoting) frequencies, that form the central pattern of a much wider self-similar EMF spectrum of cancer inhibiting or promoting activities. Inhibiting of the cancer process, and even curing of the disease, can thus be considered through exposure to the coherent type of EM fields. Stabilization of the disease can be understood by constructive resonance of macromolecules in the cancer cell with the externally appied coherent EMF field frequencies, called solitons/polarons. The latter, for instance, have been shown earlier to induce repair in DNA/RNA conformation and/or epigenetic changes. The field of EMF treatment of cancer disorders is rapidly expanding and our studies may invite further experimental and clinical studies in which systematically various potential EMF treatment protocols could be applied, with combined and modulated frequencies, to obtain even more efficient EMF anti-cancer therapies.


Introduction
The present study was performed to provide a systematic overview of electromagnetic (EM) frequencies that influence cancer processes, through a meta-analysis of earlier scientific reports on the effects of EM fields on life systems in vitro and in vivo, in the framework of cancer experimentation.A second aim was to apply these data to further unravel the biomolecular and biophysical mechanisms that may play a role in this widespread group of diseases, with special reference to the role of a discovered semi-harmonic oscillatory wave pattern system of cellular macromolecules that determine a proper functional structure of the cell.
The entire list of relevant data out of the investigated literature can be found in Appendix, beneficial frequencies and detrimental frequencies, while further details of the experiments analyzed can be found in Appendix 1.Studies were included in the present meta-analyses on the basis of, mostly, peer reviewed articles, using well defined radiation technology and exposure characteristics, containing statistically significant and reproducible data as well as clearly describtion of the particular positive or negative effects.A, single glimpse, overview of the present results is depicted in Figure 1.
Fröhlich pioneered in this approach by proposing that the functionality in living systems results from ordered vibratory states influencing the apparently chaotic motions and arrangements of biological molecules.An important feature is that ordered or coherent states can be manifest over large distances, thus offering a mechanism by which cells can intercellular and intracellular communicate, in addition to the known short range chemical forces.This long-range biological coherence provides the growth control as it exists in healthy tissue but is absent in cancer [1].A number of investigators have expanded Fröhlich's Figure 1.Solitons propagate in either direction, exchange positions and eventually return the system to states that resemble their initial configuration.The motion of the solitons can be seen here by following the lines of colours, which denote displacements (From Porter, 2009 and image from Zabusky, Sun and Peng 2006).
If cells, bio-molecules, and cell networks are organized such that coherency of waves and wave patterns is at stake, a physical relation should exist between this property and the stability of the components.A coherent pattern within a life-algorithm of electromagnetic field-frequencies for living cells was earlier inferred by us in a meta-analysis of bio-medical literature [12] [13].The observed coherent resonances in life systems were subsequently matched to a Pythagorean scale of tuning and octave hierarchy.Interestingly a similar set of frequencies was earlier detected in non-animate systems: the particular EM frequencies turned out to be related to eigenvalues of a square oscillating plate (Ritz, 1909).We inferred that living organisms function against a background of such coherent resonances, at the level of molecules, their functional aggregates, overall cell architecture and and possibly even at the neuronal level of conscious perception [14].Coherency may be related to solitons that play a role as self-reinforcing solitary waves and are seen as electromagnetically longitudinal, helical and radial waves that travel along proteins, microtubules and DNA (ref).They thereby may induce an endogenous coherent electromagnetic field and stabilize local resonant oscillations and/or induce electronic excitations of neighbouring molecules and macromolecules.The corresponding soliton frequency-zones are considered to be responsible for the coherent wave patterns in cells.It was hypothesized by us that such wave energies are collected in, so called, underlying toroidal space-time operators and that the particular multi connectedness can be optimally expressed by adopting a toroidal geometry [14].From these studies a bio-soliton model has been derived that describes a spectrum of electromagnetic eigen-frequencies of which coherent and non-coherent frequencies are ordered in an alternate fashion.This knowledge can be applied to understand physical principles of biological effects in living cells, as caused by electromagnetic fields [13].The model is complementary to Henry's model of characteristic frequencies involving water molecules by relating the molecular weight M of any solvent or solute species to EM frequencies, using the mass-energy equivalence coupled to the Planck-Einstein relationship [11].
We envision that a resulting soliton based morphogenetic field provides a dedicated control of functional shape of life structures, through bringing in positional information and cues, in order to regulate organism-wide system properties like cellular architecture, including control of reproduction and repair.It is proposed that the most optimal architectural state of a living cell is such a coherent state, and that decline of quality of cell properties can occur when a transition takes place from coherent states to states of less coherence, that can lead to moderate no-coherence or even to a state a full non-coherence.
The highest coherent state can be defined as an integral fine tuned assembly of such coherent soliton frequencies.Our soliton model may predict which discrete eigen-frequencies of non-thermal electromagnetic waves are life-sustaining and which are not.The particular effects were found to be exerted by a range of electromagnetic wave frequencies of one-tenth of a Hertz till Peta Hertz (at Hz, KHz, Mhz, GHz, THz en PHz), and showed a distribution pattern of twelve

Hypothesis: Cancer Is Due to a State of Loss of Internal Cellular Organization and em Coherence
Various physical models about the origin of carcinogenesis on the basis of biophysical mechanisms were proposed earlier.In the following, we will shortly treat a selection of these theories: Plankar et al.
Cancer was postulated to be essentially a non-genetic disease, characterised by a global and unspecific impairment of energy and information flow through the system, as manifested in genomic, transcriptomic and proteomic dysregulation.
It is primarily characterized by an unspecific progressive self-disorganisation, and impairment of the proper coherent dynamics at some specific levels [16] [19].

Sonnenschein and Soto
Carcinogenesis was seen as a problem of tissue organization: carcinogenic agents destroy the normal tissue architecture disrupting cell-to-cell signaling and thereby compromise genomic integrity.Single or multiple carcinogenic exposure acts in a given morphogenic field, disturbing the reciprocal biophysical communication between the parenchyma and the mesenchyme/stroma [17] [18].

Pokorný et al.
Impaired coherence was linked to the bioenergetic aspect of cancer considering Fröhlich's theory.Cancer has a lower degree of overall coherency.Healthy cells and the organization of living matter depends on a morphogenetic pattern formation, and a field that determines the morphological structure of living organisms [16].
Levin and Chernet Cancer was interpreted as corrupted geometry: a misregulation of the field of information that orchestrates individual cell activity with regard to normal anatomy.The view that cancer is a developmental disorder, predicts that molecular mechanisms, known to be important mediators of the supposed morphogenetic field, are deranged and thereby would be involved in tumorgenesis.Failure of morphostasis can occur in cancer, because the entite morphogenetic field is missing, altered, or not successfully perceived.This can occur due to selective genetic or physiological state changes [20] [21] [22].

Knox and Funk
A context dependent model was focused on interactions between the cell and its surrounding environment as the initiator and/or driver of malignancy.Ge- may contribute to carcinogenesis and pathological alterations, resulting in many chronic disorders [24].

Tuszynski et al.
A non-uniform field will lead to the development of dielectrophoretic forces, acting on polarizable macromolecules such as microtubules, and organelles.This can affect all charged structures present in the cell, such as ions, proteins or DNA.A model has been proposed, related to ionic solitary condensation waves around microtubules.In addition dielectrophoretic effects in dividing cells may act on the dipole moments of microtubules at intermediate frequencies.The whole cytoskeleton, and especially microtubulins, participate in numerous collective interactions with electromagnetic forces, due to the complex charge distribution in and around the particular protein filaments that are surrounded by poly-ionic solutions.Solitary ionic waves have been described as solutions of a nonlinear partial differential equation [25].

Popp
Biophoton emissions from healthy humans display rhythmic patterns and show coherence.Biophotons emitted from cancer cells lack coherence and fail to follow natural rhythmic patterns.Popp hypothesized that cancer results from a disruption of cell's photorepair system and discovered that benzo[a]pyrene, a potent carcinogen, absorbs ultraviolet light at 380 nanometers and emits it at another frequency [26] [114].

Le Chapellier and Matta
An explanation of the action mechanism of solitons upon pancreatic tumor is proposed.A non-linear system which emits dissipative solitons is sensitive to the presence of an external structure of frequencies.According to biophysics, the exposure of the cellular medium to solitons sensible for radiofrequencies tends to produce a coherent structuring [27]. in vitro and in vivo [43] [44].A combined treatment of PEF (pulsed electromagnetic waves) and Co-gamma radiation shows a significant effect on delaying the growth of glioma and subcutaneously implanted tumors [45].
Stem cell biology have opened a new window in the expanding area of regenerative medicine based on tissue engineering and cell therapy derived from a variety of stem cells.Effects of EMFs on human adult stem cell biology have been studied, such as proliferation, the cell cycle, differentiation and properly adjusted values of EMF frequencies, as well as times of stimulation [24].Neurogenesis and osteogenesis processes rely on the activation of specific and complex transcriptional programs, while epigenetic mechanisms play a critical regulatory role.This can be realized by translating a wide array of endogenous and exogenous signals into persistent changes in gene expression in both neural stem cells and mesenchymal stem cells.EMF stimulation has been recognized as an effective tool in promoting both neurogenesis and osteogenesis and the studies performed, so far, point to chromatin remodeling and pro-neuronal gene expression [46].

Coherence versus Loss of Coherence in Relation to Cancer
The organisation of components of a life system can be logical and well-organized in a biological sense or show chaotic aspects, which is often related to the terms coherent or non-coherent respectively.Of note, the organised pattern of the cell components can be stable, or instable as well as in equilibrium or far from equilibrium.In physics, waves are called coherent when the phase differences between the waves is small, whereas, if waves are defined as incoherent, these phases have a high degree of variability [14].We proposed that life bio-molecules and viable cells are exposed to and are functioning within about 400 Hz narrow EM field frequency bands over a broad spectrum of frequencies.The individual values that form quite narrow frequency bands, are localized around highly coherent frequencies.They, apparently, fit with a discrete pattern of coherent waves and, in our view, may be co-responsible for the architectures of living cells.The particular, highly coherent, frequencies of living cells/molecules are thus positioned in "coherent zones" and exist within in a small bandwidth of 0.85% of the local coherent algorithmic frequency.In contrast, non-coherent zones are positioned just in between the coherent zones and are responsible for a destabilization of cellular organization, also within a small bandwidth of 0.85% of the local decoherent algorithmic frequency.Cell-sustaining properties are posi-tioned at the green points, see Figure 2, while cell-destabilizing non-coherent frequencies are positioned between the cell-sustaining frequency bands at the red squares.We proposed: 12 coherent reference semi-harmonic frequencies: 256, 269.2).All other frequencies, situated below or above the range of Figure 2, can be simply derived by octave hierarchy.
Fröhlich did already present the first explicit hypothesis on the role of coherence in cancer and laid the basis for understanding the related physical processes in biological systems.The central item is that cancer transformation pathways include a link with altered coherent electric (electromagnetic) vibrations.He proposed that a global (localy extended) coherent excitation emerges from electrically polar structures of sufficient size and polarisation density spans across the tissues.These may also exert a long-range communication between cells, thereby electro-mechanically stabilising the whole tissue.A cancer cell may escape from such interactions with the surrounding healthy cells and individual cells may then exhibit independent activity, that is if the frequency spectrum is perturbed and/or shifted.Such frequency changes may be combined with disturbances of the spatial pattern of the field by which the transformed cell becomes dissociated from local interactions and tends to perform local invasion and formation of metastases.When a critical number of cells cease to be in resonance with the global local excitation, they will no longer be under tissue control and will express their tendency to divide again, a state which Fröhlich identified with cancer [50] [51].
Devyatkov has considered the same principle of interactions of biomolecules and living cells.He found that biological effects of cells, exposed to electromagnetic Figure 2. EM frequencies that were experimentally applied to living cells systems reported in 219 separate biomedical studies, plotted on a semi-harmonic logarithmic reference GM-scale, are found to be patterned in 12 apparent bands of in total 143 life-sustaining coherent frequencies (green points) and 77 cell-destabilizing non-coherent frequencies (red squares).The latter are clearly positioned between the life-sustaining frequency bands.Each point indicated in the graph represents an individual experiment.For clarity, points are evenly distributed along the Y-axis, according to the number of experiments within each apparent frequency band.
waves, are dependent on: wavelength, wave modulations, dose, exposure time, magnetic field and coherence.He discovered that cells may be affected by long series of combined frequencies, to be considered as second and third harmonics of these frequencies, providing oscillations of a, so called, collective mode [53] [54] [55].
Also Popp has hypothesized that cancer results from a disruption of cells' photorepair system and that biophoton emissions from cancer cells lack coherence and fail to follow natural rhythmic patterns [26].
Our proposed soliton model describes that a high level of coherence of waves for healthy living cells is realized when the absolute distance between a distinct endogeneous or exogeneous frequency in relation to a coherent frequency is positioned in the soliton algorithm in the range of 0.0% -0.85% of the particular value.A moderate level of coherence is defined when the absolute distance between a typical frequency and a calculated soliton coherent frequency is between 0.85% -1.25%.A clear decay of organizational frequencies of living cells can occur when the absolute distance between the observed frequency and the calculated coherent frequency is between 1.25% -2.50%, while a maximum decay can take place around 2.50% -3.0% [13].About 400 typical coherent solitonic frequencies were detected in literature to sustain healthy living cells.This implies either an endogeneous and or an exogeneous filed, yet both can be modeled as vortex like movements if positioned on a toroidal rotatory structure.About 400 typical decoherent solitonic frequencies sustain the organizational decay of healthy living cells and can be positioned at the vortices of a toroid [13].The torus, like a twistor, is seen as the basic space-time structure, acting as an operator for the processing of quantum wave information.

Prevention of Carcinogenesis and Collective Evidence for Our EM-Mediation Hypothesis
Carcinogenesis is, according to H. Fröhlich, Davydov and the earlier discussed models, conceived as having a relation with the above mentioned "organized field", and thus with electrodynamics in and around living bio-molecules/cell(s).
The "organized field" is supposed to interact with EM vibrations such as solitons that represent nonlinear interactions of vibrational excitations in and around biomolecules at typical frequencies [13].Solitons are self-reinforcing solitary It can be further confirmed that carcinogenesis and cancer growth is likely to be associated with a non-coherent character of electromagnetic waves and related quantum states.On the other hand, inhibition and curing of cancer turn out to be coupled to a coherent behavior of electromagnetic waves and quantum states, according to the proposed algorithm of frequencies.Importantly, it Figure 3. EM frequencies (in total 95) that were experimentally applied to living cells systems, and plotted logarithmically on an acoustic algorithmic GM-scale, are found to be patterned in 12 apparent bands of cell-sustaining coherent frequencies that are able to inhibit/retard cancer (green points) and non-coherent frequencies able to initiate/promote/represent cancer (red squares), the latter are positioned between the cell-sustaining frequency bands.Each point indicated in the graph represents an individual experiment as registered in 123 biomedical studies on cancer.For clarity, points are evenly distributed along the Y-axis, according to the number of experiments within each apparent frequency band.
follows that curing or inhibition of cancer can be achieved by exposure to electromagnetic frequency conditions that are beneficial for cells.
Subsequently, the different frequency effects of electromagnetic waves on living cells were also analysed with regard to cell differentiation, DNA compostion, chromosomal aspects, genetic expressions, genome-wide methylation, foci in differentiated cells, stem cells, neurons, plasma membranes, germ cells, signalling path ways, cognitive effects, learning, spatial memory, and cell death among others (Appendix 2).

Direct Measurement of EM Wave Frequencies in Tumor Tissues
Endogeous measurements at EM MHz frequencies in cancer cells, fully supported the proposed hypothesis.Damping of external electromagnetic field caused by cancer tissue has been for example measured at a frequency of 465 MHz including the first harmonic.The absorption resonant frequencies of some tumors around 465 MHz was estimated as a distinct shift of spectral lines of normal cells (Vedruccio, 2004(Vedruccio, , 2011)), see Appendix 2.
The principle of detection lies in the resonance between the coupled active nonlinear oscillator (the probe) and the passive oscillator (the tissue) in the radiofrequency range of the electromagnetic spectrum.play also a key role in the use for tissue engineering [112].The ability to interconvert information between electronic and ionic modalities has transformed the ability to record and actuate biological function.Electronic actuation of the native transcriptional regulators and transcription from promoters allows cell response that is quick, reversible and dependent on the amplitude and frequency of the imposed electronic signals [116].

General Discussion of Overall Results
We have previously shown that about 200 typical coherent EM-frequencies sustain the viability of living cells, and that the particular values are precisely positioned in, so called, coherent frequency bands.Exposure to about 150 typical non-coherent EM frequencies, produce unhealthy cells and turned out to be precisely positioned in the non-coherent frequency bands.The particular bands, that presumably represent soliton frequency zones, show a discrete distribution pattern, if plotted on an acoustic standing wave scale, called a semi-harmonic reference GM-scale (Figure 2).The distribution pattern shows a clear separation of the bands in a statistically significant manner.The pattern of twelve basic frequency intervals and bands could be adequately described by an acoustic algorithm.We regard this dicrete pattern of wave activities as a morphogenetic code, indicating a semi-harmonic vibration modality [12] [13].
Many published data now support the hypothesis that cancer can be initiated and promoted at typical frequencies of electromagnetic waves.The reported frequencies are apparently positioned in the same decoherent soliton frequency zones identified by us.In contrast, according to these studies, cancer can be inhibited and retarded in the discrete coherent soliton frequency zones inferred from our studies (Figure 3).The particular results are rather striking: nearly all Of the overall studies, biological phenomena of healthy living cells are positioned in zones of beneficial coherent soliton frequencies, at a mean distance value around a coherent frequency of 0.78% (for continuous wave exposures), whereas unhealthy living cells are located in zones of detrimental decoherent soliton frequencies at a mean distance value from a coherent frequency of 1.86% (for continuous wave exposures).
Interestingly, in the investigations into the influence of EM frequencies that potentially induce cancer disorders, as listed in the Appendix 1, as much as 39 different values of electromagnetic waves make use of so called carrier waves that in our scheme in fact represent coherent soliton frequency bands, but of which the applied wave modulations that are superposed on the particular carrier waves belong, in contrast, to the decoherent soliton frequency bands.These kind of complex superposed waves therefore show an overall decoherent behaviour, resulting in detrimental biological properties.According to our calculations the overall mean distance from the respective coherent frequencies of these kind of waves amounts to 1.80% -2.00% and therefore, in our definition, therefore become highly incoherent.
It is further remarkable that living cells remain viable over a wide regime of electromagnetic wave radiations, with typical frequencies and modulations, and all are fitting into an electromagnetic range of frequencies, from about less than one Hertz till one peta Hertz (10 15 ).In addition, the idea of selective zones of life/supporting or life endangering frequencies, was supported both by direct tissue measurements of typical endogeneous EM frequencies in healthy tissues, as opposed to endogeneous frequencies in cells with cancer features.
In general, the present study highlights the existence of a dominant vibrational spectrum of EM fields that, as an "algorithm of living cells", also may have played an evolutionary role in the initiation of first life and in the stabilization of life systems, until today.At the same time this principle of physics, as defined in our recent papers, can influence our health if the nature of the coherent frequencies is perturbed so that non-coherent frequencies, that is of sufficient density and exposure times, take over.With this knowledge it will be possible to develop innovative technologies that can effectively improve the life-sustaining coherency of electromagnetic signals.

Potential mechanisms of EMF in cancer disorders
The mechanisms behind the life-sustaining and life-disturbing field effects of the spectrum of externally applied EM frequencies (including some directly measured values in normal and diseased tissues), as reported in the biomedical publications analyzed by us, can in principle be described on the basis of current biophysics: The particular EM frequencies resonate with discrete vibratory macromolecules in the cell, producing domains of coherent wave patterns in proteins, cell water and/or DNA (Del Giudice [6]; Fröhlich [1]; Pang et al. [122]; Meijer and Geesink [14]; Melkikh and Meijer [121]).Coherence is seen by us a fundamental property of quantum biology and can be defined as the physical congruence of wave properties within wave packets and is a property of stationary waves (i.e. temporally and spatially constant) that enables a type of wave interference, known as constructive.This can lead to stabilizing internal vibratory patterns crucial for life conditions, as may have also been selected in biological evolution.
Thereby, these waves are instrumental in beneficial influences on cell metabolism, intercellular information transfer and morphogenetic stimuli.Such coherent vibration patterns can also explain the long-range interactions between distant cell groups, as reviewed by Cifra [81].We have earlier reported on the potential effects of solitons on protein folding as a long range mechanism [121].
The detrimental frequencies, detected by us, may cause non-coherent resonance by destructive resonant interference.It should be stipulated here that the life disturbing frequencies found were called by us non-coherent, yet this should not be confused with the term decoherence as the loss of quantum coherence due to interaction with the environment.The supposed coherent wave patterns (see Fröhlich, [1]), and dual (symmetric) wave/matrix interactions (see Pang et al. [122]) have been demonstrated by spectroscopic methods among others in proteins (Lundholm [5]; Bandyopadhyay [125]).The particular wave modalities could both have a quantum and classical character, the latter if sufficient cellular energy is supplied (Nardecchia et al. [123]).
The experimentally applied EM fields of the analyzed studies may mimic naturally occurring, terrestrial electro-magnetic patterns of the atmosphere and typical minerals present in the top-layer of the earth, probably including pre-mordial modalities, that have influenced the informational and structural organization of pre-biotic and first life cells as well as in in present life organisms (Melkikh and Meijer [121]; Melkikh, [124]).As discussed in our previous work [13] [14] [118] [119], especially polarized and cyclotron-like waves can directly perturb ion-channel proteins as demonstrated for Ca 2+ , an ion that is central in cell regulation.

State of Art of EMF Therapy and Further Perspectives
The field of EMF treatment of cancer disorders is rapidly expanding [127]- [173].
Recently a large number of in vitro and in vivo studies were published on the an- 10456.4Hz) may block proliferation of cancer cells both in vitro as well as in vivo at levels of exposure similar to those yielding therapeutic responses in hu- mans [158].However the applied frequencies are located at the non-coherent frequencies described by the present GM-scale.Methodological differences (direct measurement in cancer tissues versus our meta-analyses of biomedical literature) may be at stake.Yet we found several studies with direct tissue measurements in line with our GM algorithm (see section 6).Furthermore our GM-analysis shows that a more robust treatment might be realised by applying multiple coherent frequencies according to the proposed coherent frequency scale.Interestingly, Cosic's Resonant Recognition Model (RRM) postulates that biological processes/interactions are based on electromagnetic resonances between interacting biomolecules at specific electromagnetic frequencies.This model approach deals with the infra-red, visible and ultra-violet frequency ranges, where each interaction can be identified by a certain frequency critical for resonant activation of specific biological activities of proteins and DNA [159].The various biological interactions could be grouped according to their resonant frequency into super families of these functions, enabling simpler analyses of these interactions and consequently the analyses of influence of electromagnetic frequencies to health.According to Cosic, the RRM spectrum of all analyzed biological functions/interactions is similar to the spectrum of the sunlight on the Earth.The relative differences between the mean values of the proposed RRM spectrum between interacting biomolecules at specific electromagnetic frequencies and the mean frequency values of our algorithmic GM-scale for various life systems in vitro and in vivo amount to 2% or higher.The latter points to a statistical dif-D.K. F. Meijer ference that, according to our criteria, is too large to find an apparent correspondence between both models.Yet, a more systematic comparison of the respective data would be attractive.Extremely low frequency (ELF) pulsed-gradient magnetic fields, not only induce changes in cell cycling [105]), but also may seem to block neovascularization required for tumour growth [153]).Cameron et al. [130] [131] showed that gamma irradiation IR or EMF therapy in mice had fewer lung metastatic sites and slower tumor growth, compared with controls.

Preliminary clinical work
Preliminary clinical results in various tumour types such as recurrent glioblastoma's, hepatocellular carcinomas and breast carcinomas showed perspectives.Many studies focused on low-frequency (<300 Hz) magnetic fields with simple or symmetrical (sine-or square-wave) patterns to affect cellular processes.
Some studies have shown that exposure to a low frequency EMF pattern can promote cell proliferation while others have shown that EMF exposure inhibits cell proliferation, in line with the present study.EMF therapies may reduce proliferation and induce apoptosis in different cancer cells such as osteosarcoma, breast cancer, gastric cancer, colon cancer, and melanoma.Marchesi et al. [145] showed that autophagy is induced upon EMF exposure in neuroblastoma cells and also tumor vascularization can be inhibited in vitro and in vivo in breast cancer.EMF therapy decreased tumor growth in mouse models of malignant melanoma, colon carcinoma and adenocarcinoma.Costa et al. [135] showed clear clinical benefits from using the specific AM-EMF signals to treat advanced hepatocellular carcinoma, also with partial responses up to 5 years in some of the patients.

Potential mechanisms and types of EMF exposure
Exposure of cells to 20 -60 Hz EMF patterns has further been shown to affect signal transduction pathways with effects on cAMP levels, MAP kinase activation, Ca 2+ -calmodulin kinase activation, or Ca 2+ channels [102] [129].It is important to note that the inhibitory response can be strongly field-strength and exposure-time dependent.It was hypothesized by Buckner et al., [129], that the ability of EMFs to interact with biological processes is dependent on the temporal patterns of the fields, similar to the way anti-cancer agents are dependent on their structures.Therefore, the information chosen in a specific time-varying pattern, also at low intensities (5 -10 μT), could influence biological processes.The characteristics of an EMF that elicit biological responses should be specific for wave pattern, field strength, and exposure configuration.Barbault et al. [126] reported on specific frequencies for different tumour diagnoses, which are then used in the amplitude-modulated (AM)-EMF treatment of those patients to stabilize the disease beyond normal expectations.

Combination of EMF with radio and chemotherapy
Various studies [132] [153]- [160] showed the potential of EMF therapy in combination with conventional cancer therapies as new approach for sensitizing tumors.Also here, the applied EMF patterns show great differences in intensity, Hz wave with a typical modulation: -Nucleosome-sized DNA fragmentation (a biochemical marker of apoptosis) was induced in human myelogenous leukemic cell lines, HL-60 and ML-1, when exposed to 50 Hz electromagnetic fields.This 50 Hz wave did not induce detectable DNA fragmentation in either human peripheral blood leukocytes or polymorphonuclear cells (Hisamitsu, 1997).-Human colon adenocarcinoma and human breast adenocarcinoma exposed to 3 mT static MF, modulated in amplitude with 3 mT ELF-MF at 50 Hz, showed morphological evidence of increased apoptosis (Tofani 2002).
-Anticancer activity of electromagnetic fields was observed by exposing mice bearing a subcutaneous human breast tumour to modulated MF extremely low frequency fields at 50 Hz at an intensity of 5.5 mT (Tofani 2003).
-Increased apoptosis in human breast cancer cell lines occurred by exposure during 24 and 72 h to pulsed EMF (50 Hz; 10 mT) compared with untreated control cancer cell lines (Filipovic, 2014).-50 Hz modulated with a sufficient high level of incoherent frequencies is able to cause cancer at a relatively low field strength.50 Hz combined with a harmonic distortion of about 3% can cause cancer in rats at field strength of 1000 µT in mice after 800 days (Soff.2016).But an estimated lower content of inharmonic distortions no cancer in animals (rats) at a strength of 500 µT occurs after 2 years (of note: 50 Hz is positioned in a zone with a moderate coherence), (Yasui, 1997).
-60 Hz with a sufficient amount of harmonic distortion can cause cancer at a field strength of 200 µT in mice after 852 days at an amount of harmonic distortion less than 3% (Boorman, 1999a).But a 60 Hz with a low amount of harmonic distortion did not cause cancer in animals at a high field strength of 1420 µT in mice after 852 days (of note: 60 Hz is positioned near the border of low coherence), (McCormick et al., 1999).
-A significant decrease in the rate of tumor growth and increase in survival were observed for male and female mice exposed for 8 h/day to 100 mT, 0.8-Hz square-wave from the onset of tumor until death or until the tumor volume reached a predetermined volume (Seze, 2000).
-A significant decrease in cell growth (56%) of colon adenocarcinoma cells has been shown in cells exposed to 1Hz or 25 Hz for 2 till 6 h. at 1.5 mT in the presence of dexamethasone (Ruiz-Gómez, 1999, 2002).
-The inhibition growth rate was significantly higher of murine osteosarcoma cells, treated with doxorubicin in the presence of 10 × 10 −3 mT PEMF at 10 Hz, compared to both non-exposed resistant cells and those non-treated with doxorubicin (Miyagi et al., 2000).
-Mice inoculated subcutaneously with B16-BL6 melanoma cells exposed to 25 Hz EMF for 3 h did not grow tumours after 38 days, however, the mice in the sham-field and reference controls showed massive tumours.Tumour growth was also affected by the intensity of the field, with mice exposed to a weak intensity field (1 -5 nT) forming smaller tumours than mice exposed to sham or stronger, high intensity (2 -5 microT) fields (Hu JH, 2010).Journal of Cancer Therapy -Exposure of mice injected with mouse breast cancer cells to electromagnetic fields, for 6 h.daily at 100 mT, 1-Hz, half-sine-wave unipolar magnetic fields for as long as 4 wk, suppressed tumor growth (Tatarov, 2011).
-Rat liver cancer exposed to 0.9 Hz and 3.0 Hz magnetic fields at 13 -42 Gauss and 0.6 Tesla showed apoptosis, necrosis and inflammatory infiltration of the malignant carcinoma (Emara, 2013).
-Electromagnetic exposure by 0.4 T, 7.5 Hz for 43 days inhibited the growth and metastasis of melanoma cancer cells and improved immune function of tumor-bearing mice (Nie Y., 2013).
-Microarray of human A549 lung adenocarcinoma cells exposed for 1 hour to 8 Hz electromagnetic wave showed a duration-dependent inhibitory effect and the cell cycle and apoptosis-related genes had 2-fold upregulation and 40 genes had 2-fold downregulation (Feng, 2013).
-Pulsed EMF at 20 Hz and intensity of 3 mT during 3 days showed cytotoxic to breast cancer cells (Crocetti, 2013).
-The effect of the A3AR agonist in tumor cells was enhanced in the presence of pulsed EMFs and blocked by using a well-known selective antagonist.The results demonstrated that pulsed EMF exposure significantly increased the anti-tumor effect modulated by A3ARs at a pulse duration of 1.3 ms ( 1300Hz) and frequency of 75 Hz (Vincenzi, 2012).
-Human hematoma cell line cells decreased with a variety of Xray irradiation doses combined to 100 Hz EMF at 0.7 mT and cause accumulation of apoptotic effects in BEL-7402 cells (Jian et al., 2009).
-Five periods of combined 100 Hz 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 alone.A greater number of 100 Hz MF exposure periods could further improve the survival and inhibit tumor growth in hepatoma-implanted mice when combined with 4 Gy X-ray (Wen, 2011).
-Exposure of breast tumors to a 120 Hz magnetic field 10 minutes per day with 0, 10 mT, 15 mT or 20 mT significantly reduced tumor growth, reduced the percentage of area stained for CD31 indicating a reduction in the extent of vascularization and there was a concomitant increase in the extent of tumor necrosis (Williams, 2001).
-Male Fischer-344 rats subjected to the modified resistant hepatocyte model and exposed to 4.5 mT -120 Hz ELF-EMF inhibited preneoplastic lesions chemically induced in the rat liver through the reduction of cell proliferation, without altering the apoptosis process (Jiménez-García, 2010).
-Exposure to 20 mT for 10 minutes 120 Hz semi sine wave pulse signal of variable intensity of murine 16/C mammary adenocarcinoma tumor fragments reduced the vascular volume fraction and increased the necrotic volume of the tumor (Cameron, 2005(Cameron, , 2014)).-Modulated RF field of 900 MHz with a 8:1 pulsed signaling system at a SAR of 1 W/kg induced anti-proliferative activity in human neuroblastoma SH-SY5Y cells, also the appearance of the sub-G1 peak, a hallmark of apoptosis, was highlighted after a 24-h exposure, together with a significant decrease in mRNA levels of Bcl-2 and survivin genes, both interfering with signaling between G2-M arrest and apoptosis (Buttiglione, 2007).
-A study of ablation efficiencies revealed that 18-GHz microwave results in the largest difference in the temperature rise between cancer and normal tissues as well as the highest ablation efficiency, reaching 20 times that of 2 GHz.Thermal profile study on the composite region of cancer and fat also showed significantly reduced collateral damage using 18 GHz.Application of low-power (1 W) 18-GHz microwave on the nude mice xenografted with human breast cancer cells resulted in recurrence-free treatment.The proposed microwave ablation method can be a very effective process to treat small-sized tumor with minimized invasiveness and collateral damages (Yoon, 2011).
-Coherent monochromatic frequency signals at GHz are able to suppress tumor growth (Radzievsky, 2004;Beneduci, 2005).The biological effects produced by low power millimeter waves (MMW) were studied on the RPMI 7932 human melanoma cell line.Three different frequency-type irradiation modes were used: the 53.57-78.33 GHz wide-band frequency range, the 51.05 GHz and the 65.00 GHz monochromatic frequencies.In all three irradiation conditions, the radiation energy was low enough not to increase the temperature of the cellular samples.The wide-band irradiation treatment effectively inhibited cell growth, while both the monochromatic irradiation treatments did not affect the growth trend of RPMI 7932 cells (Beneduci, 2005).
-A coherent pulsed electromagnetic field at a coherent MHz frequency is able to reduce cancer in a cell lines (Agulan, 2015).
-Electric pulses 20 ns or less kill a wide variety of human cancer cells in vitro, -Noninvasive electroporation was performed by magnetic field pulse generator connected to an applicator consisting of round coil.Subcutaneous mouse B16F10 melanoma tumors were treated with intravenously injection of cisplatin, PEMF (480 bipolar pulses, at frequency of 80 Hz, pulse duration of 340 μs) or with the combination of both therapies (electrochemotherapy-PEMF + CDDP) (Kranjc, 2016).
-Tumors in treated mice showed nsPEF-mediated nuclear condensation (3 h post-pulse), cell shrinkage (1 h), increases in active executioner caspases and terminal deoxynucleotidyl transferase dUTP nickend-labeling (1 h) with decreases in vascular endothelial growth factor expression (7d) and micro-vessel density (14 d).Tumors disappeared with 100 ns pulses to nearly non-detectable levels 14 -21 days after the first treatment in 6 of 8 mice.Optimal treatments included 76.5% tumor-free survival for nearly 9 months (Chen X, 2012).
-Nanosecond pulse electric fields (nsPEFs) ablate melanoma by induction of apoptosis and inhibition of angiogenesis.Four hepatocellular carcinoma cell lines HepG2, SMMC7721, Hep1-6, and HCCLM3 were pulsed to test the anti-proliferation and anti-migration ability of 100 ns nsPEFs in vitro.The animal model of human subdermal xenograft HCCLM3 cells into BALB/c nude mouse was used to test the anti-tumor growth and macrophage infiltration in vivo (Chen X 2014).
-NsPEF could not only induce cell apoptosis via dependent-mitochondria intrinsic apoptosis pathway, but also inhibit cell proliferation through repressing NF-κB signaling pathway to reduce expressions of cyclin proteins.-To determine if nanosecond pulsed electric fields (nsPEFs) is equally effective in treatment of human breast cancer, 30 human breast cancer tumors across 30 Balb/c (nu/nu) mice were exposed to 720 pulses of 100 ns (7.2 GHz) duration, at 4 pulses per second and 30 kV/cm.Two weeks after treatment, the growth of treated tumors was inhibited by 79%.Pulsed tumors exhibited apoptosis evaluated by TUNEL staining, inhibition in Bcl-2 expression and decreased blood vessel density.Notably, CD34, vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) expression in treated tumors were strongly suppressed.The results suggest nsPEFs is able to inhibit human breast cancer development and suppress tumor blood vessel growth, indicating nsPEFs may serve as a novel therapy for breast cancer in the future (Wu S., 2013).
-Exposing the tumor tissue female Balb/c mice to 10 MHz modulated 4.5 Hz, 2 Gauss square wave magnetic field for 2 weeks at a rate 2 hours/day inhibited tumor growth and increased the survival period of the animals.However, group B showed more improvements than did group C that was attributed to some distortions in the square waveform.The use of typical ELF EMF at 0.5 Hz and 0.7 Hz electric field exposed to Balb/c mice g carrying Ehrlich tumor proved that tumor cells can be controlled and recovery of rgans such as liver and spleen are possible (Fadel, 2011(Fadel, , 2015)).
1.8) Mhz and GHz frequencies located in decoherent-zones may cause cancer -Human cells exposed to continuous 830 MHz electromagnetic fields at 2.6 -8.8 W/kg at a nonthermal level can lead to acquire premalignant genotypes associated with elevated levels of aneuploidy and abnormalities in replication mode as expressed in asynchrony in the replication timing of homologous chromosomal regions associated with chromosome segregation.These findings support the view that exposure to this kind of RF radiation of average SAR values of 2.6 -8.8 W/kg can lead to a genotoxic effect of the electromagnetic radiation and may lead to a carcinogenic activity through a non thermal pathway (Mashevich, 2003).
-Male rats of wistar strain exposed to modulated 2.45 GHz, at an absorption rate (SAR) of 0.11 W/Kg, showed a significant increase in comet head, tail length and in tail movement in exposed brain cells.An analysis of antioxidant enzymes glutathione peroxidase and superoxide dismutase showed a decrease while an increase in catalase was observed.The study concludes that the chronic exposure to these radiations may cause significant damage to brain, which may be an indication of possible tumour promotion (Kesari, 2010).
-Changes in the overall pattern of protein phosphorylation suggest that incoherent modulated 900 MHz activated a variety of cellular signal transduction pathways, among them the hsp27/p38MAPK stress response pathway.Based on the known functions of hsp27, a hypothesis has been put forward that this kind of electromagnetic fields induced activation of hsp27 may facilitate the 1.9) Mhz, GHz, THz frequencies located in decoherent zones can cause cancer (table 2b) -Low-level laser therapy (LLLT) at 660 nm induced significantly the proliferation of a squamous carcinoma cell line SCC25 cells at 1.0 J/cm 2 , which was accomplished by an increase in the expression of cyclin D1 and nuclear β-catenin.The results of this study demonstrated that LLLT exerts a stimulatory effect on proliferation and invasion of SCC25 cells, which was associated with alterations on expression of proteins studied (Gomes Henriques, 2014).
-Laser irradiation three times once a day during three days with a 660 nm 50 mW CW laser, beam spot size 2 mm 2 , irradiance 2.5 W/cm 2 and irradiation times of 60 s (dose 150 J/cm 2 ) and 420 s (dose 1050 J/cm 2 ) respectively on B16F10 melanoma cells in a vitro study increased in the hypodiploid melanoma cells at 72 h post-irradiation, and at 1050 J/cm 2 in the vivo experiment (Frigo, 2009).
-Low level laser irradiation at 660 nm or 780 nm at 6.15 J/cm² can modify oral dysplastic cells (DOK) and oral cancer cells (SCC9 and SCC25) growth by modulating signalling pathways; LLLT significantly modified the expression of proteins related to progression and invasion in all the cell lines, and could -The mutagenic effect on Escherichia coli strains of UV radiation emitted by a XeCI laser (lambda = 308 nm, tau = 20 ns, 100 mJ pulse energy) has been analyzed as a function of the exposure dose and compared with the effect induced by 254 nm radiation emitted by a conventional germicidal lamp.Mutations can involve any genome site and therefore can give rise to various phenotypes, which then can be suitably selected.As a consequence, the impact of the induced mutagenesis is outstanding, both in scientific and industrial fields.In particular suitable doses of UV radiation can induce mutations, while higher doses can cause cell death, due to the induction of manifold damages to DNA (Belloni, 2005).
-The action spectrum (sensitivity per incident photon as a function of wavelength) for melanoma induction shows appreciable sensitivity at 365, 405, and probably 436 nm, as shown in heavily pigmented backcross hybrids of the genus Xiphophorus (platyfish and swordtails) that are very sensitive to melanoma induction by single exposures to UV, (Setlow 1993).
-The action spectrum of SSC (squamous cell carcinoma) has been determined  -Modulated/pulsed exposure of rats 2450-MHz EMF 21.5 h/day, for 25 months at an average specific absorption rate (SAR) of 0.4 W/kg provide an increase of malignancies (Chou CK 1992).-Mice exposed to modulated 1.966 GHz fields with intensities of 4.8 W/m (2) during 24 months displayed an enhanced lung tumour rate and an increased incidence of lung carcinomas as compared to the controls (Tillmann, 2010).
-A replication of the Tillmann study of exposed mice has been performed using higher numbers of animals per group exposed to modulated 1.966 GHz exposed at low to moderate exposure levels (0.04 and 0.4 W/kg SAR).It has been confirmed that numbers of tumors of the lungs and livers in exposed animals were significantly higher than in sham-exposed controls.In addition, lymphomas were also found to be significantly elevated by exposure (Lerchl, 2015).1.12) Mhz and GHz frequencies located in non-coherent zones with a co-carcinogen can cause cancer -Mice exposed to microwave irradiations irradiated with athermal (5 mW/cm 2 ) or subthermal (15 mW/cm 2 ) doses of 2450 MHz microwaves during 6 months resulted in a significant acceleration of the development of benzopyrene-induced skin cancer and in shortening of life span of the tumour-bearing hosts.This effect seemed to be dose-dependent since subthermal doses (15 mV/cm 2 ) and longer (3 months) expositions to microwaves were more efficient as compared to athermal doses (5 mW/cm 2 ) and shorter preirradiations (Szudziński, 1982).
-Mice irradiated by nonthermal (1 or 10 mW/cm 2 ) or thermogenic (40 mW/cm 2 ) 2450-MHz microwave (MW) fields showed a significant enhancement of the teratogenic potency of ara-C after combined exposure to both ara-C and microwave exposure during pregnancy.The possibility that specific cellular interactions of MW/RFs are connected with the pulse modulation of the carrier wave is considered (Marcickiewicz, 1986).
-Long-term exposure of mice to 2450-MHz MWs resulted in acceleration of the appearance and growth of tumors initiated by three different carcinogens, and a higher risk of cancer development in mice exposed to subcarcinogenic doses of initiators.Microwave-exposed C3H/HeA mice developed breast tumors earlier than controls (322 days in controls, 261 days for 5 mW/cm 2 and 219 days for 15 mW/cm 2 ).A similar acceleration was observed in the development of BP-induced skin cancer in mice (Szmigielski, 1982).-A diode 808 nm GaAlAs continuous wave laser has an inhibitory effect on the proliferation of human hepatoma cells line HepG2 and J-5.The mechanism of inhibition might be due to down-regulation of synemin expression and alteration of cytokeratin organization that was caused by laser irradiation (Liu YH, 2004).
-THz-pulses induced increases in the levels of multiple cell cycle regulatory and tumor suppressor proteins, favorable changes in the expression of multiple genes suggesting that cellular DNA repair machinery is activated in response to THz-pulse-induced DNA damage (Titova, 2013).Author, year (x, y, z): Author name, year of published biological experiment (applied biological frequency: x; first nearby calculated algorithmic frequency: y, percentual difference between applied frequency and nearby calculated frequency: z%).
waves and have an electromagnetic character exhibiting a longitudinal, helical and radial aspects.Organisms undergo changes in the form of successive trans-D.K. F. Meijer, H. J. H. Geesink DOI: 10.4236/jct.2018.93019198 Journal of Cancer Therapy formations of organization states of cells during morphogenesis and tissue repair[92].A first extensive meta-analysis of in total 320 published biological and medical studies has earlier been performed by us,(Geesink and Meijer, 2015, Meijer and   Geesink, 2016), in which living material (tissues, cells, and whole animals) was exposed to external electromagnetic fields employing a wide spectrum of frequencies from Hz, Khz, Mhz, GHz, THz and PHz mainly in the area of non thermal biological effects.In these studies the various effects of the electromagnetic fields were reported as to their potential to inhibit and retard cancer, as opposed to initiation and promotion of cancer.After collecting and scrutinizing the distribution pattern of these data, the following parameters were established: 1) frequency values: (Hz, kHz, Mhz and GHz, THz and PHz), 2) particular frequency modulations, 3) combinations of frequencies, and 4) chosen exposure levels.The summarized frequency data were subsequently ordened to identify the most nearby soliton frequencies, according to the proposed algorithm and subsequently to calculate the relative difference between the frequencies applied in the biological studies and the most nearby calculated soliton frequencies, and than expressed in % of the algorithmic values.The apparent frequency zones, which are located between the designated regions of stabilization and destabilization, are regarded to represent transformational zones of geometric wave patterns.The bandwidth of such frequency transformation zones were estimated to be located at about 0.50% of each local coherent frequency band To further verify this hypothesis, 123 published papers from 1965 untill now, have been re-analyzed that describe the inhibition/retardation or initiation/promotion of cancer, both in relation to the applied exogeneous electromagnetic waves.In addition some examples of supposed endogeneous EM waves were analyzed (see for the collected data of this meta-analysis the Appendix 1).A total of 95 frequency data (Hz-THz) of in vitro and in vivo biological experiments could be selected that show inhibition/retardation cancer or initiation/promotion/representing cancer.All frequency data have been normalized according to octave hierarchy and can be positioned at a normalized semi-harmonic frequency scale (Hz), called the GM-scale, see Figure 3.It can be concluded that the electromagnetic frequencies of all experiments showing inhibition/retardation of cancer are precisely positioned in frequency bands already found for cell-sustaining frequencies (green points, Figure 2 and Figure 3).All experiments showing initiation/promotion/representing cancer are precisely positioned in frequency bands already found for cell-destabilizing frequencies (red squares, Figure 2 and Figure 3).

( 96 .
2%) of the analysed 100 different EM continuous wave frequency data showed the cancer initiation/promotion or inhibition/retardation characteristics according to the proposed algorithm and fully support the present hypothesis.With regard to the specific cancer-directed studies, in total 65 frequency data analysed, showed inhibition/retardation of cancer are shown to be presicely located in zones of coherent frequencies at a mean distance value around a coherent frequency of 0.79%.The other analysed 35 frequency data, showing initia-D.K. F. Meijer, H. J. H. Geesink DOI: 10.4236/jct.2018.93019202 Journal of Cancer Therapy tion/promotion of cancer, are positioned in zones of decoherent frequencies at a mean distance value from a coherent frequency of 1.66%.The particular beneficial, versus the detrimental EM frequencies zones, that are mirrored by oscillations in the intact cell, are features of a either a healthy state or a corrupted cell state.As listed in the 123 cases in Appendix 2, the dominant biological phenomena also obey to the proposed algorithmic soliton frequencies: They include cell differentiation, genome-wide methylation and the expression of DNA, DNA strand breaks, chromosomal aberrations, genetic expressions, foci in differentiated cells, oxidative damage, stem cells, neurons, plasma membranes, germ cells, reproductive system, cognitive effects, signalling path ways, learning and spatial memory, DNA damage, and apoptotic cell death.

1. 1 )
Extremely low non-coherent frequencies can promote cancer -Unipolar and bipolar PEMF fields of 5 mT and PVMP fields of 0 mT at frequencies of 15 Hz, 125 Hz and 625 Hz were tested on cancer cell lines derived from various types of tumors: CEM/C2 (acute lymphoblastic leukemia), SU-DHL-4 (B-cell lymphoma), COLO-320DM (colorectal adenocarcinoma), MDA-BM-468 (breast adenocarcinoma), and ZR-75-1 (ductal carcinoma).Cell morphology was observed, proliferation activity using WST assay was measured and simultaneous proportion of live, early apoptotic and dead cells was detected using flow cytometry.PEMF of 125 Hz and 625 Hz for 24 h-48 h increased proliferation activity in the 2 types of cancer cell lines used, i.e.COLO-320DM and ZR-75-1.In contrast, any of employed methods did not confirm a significant inhibitory effect of hypothetic PVMP field on tumor cells (Loja T, 2014).

1. 2 )
Modulated 50 Hz and 60 Hz EM frequencies can cause cancer Incoherent modulations (positioned in decoherent-zones) added to 50 and 60 Hz carrier waves can cause cancer.-Power supply at 50 and 60 Hz contains a lot of harmonic distortion (Bulletin No. 8803PD9402, 1994; Schaffner, 2014).Due to this reason the chance on carcinogenesis and the risk of childhood leukemia increases at exposures of higher than 0.3 μT according to: National Cancer Institute Electromagnetic fields and cancer, 2016; Ahlbom, 2000; Greenland, 2000; Kheifets, 2010.

1. 3 )
Extreme low frequencies located in coherent zones can inhibit and retard cancer -Murine malignant tumour growth of mice inhibited, apoptosis of cancer cells induced, and arrest of neoangiogenesis was observed by a pulsed 0.16 -1.34    Hz treatment(Zhang X, 2002).-Growth of S-180 sarcoma in mice was inhibited by a pulsed magnetic field at 0.8 T, 22 ms, 1Hz (Chang et al., 1985).

1. 4 ) 1 . 5 )
Effects of extremely low frequencies located in coherent zones and cancer cells -Glioblastoma Multiforme (GBM) cell line (U87), in vitro, were exposed to D. K. F. Meijer, H. J. H. Geesink DOI: 10.4236/jct.2018.93019222 Journal of Cancer Therapy various ELF-PEMFs continuous square waves with 10, 50 or 100 Hz frequencies and 50 or 100 G amplitudes.The data suggest that the proliferation and apoptosis of human GBM are influenced by exposure to ELF-PEMFs in different time-dependent frequencies and amplitudes (Akbarnejad, 2016) (of note: square waves can have typical influences).Combinations of extreme low frequencies located in coherent zones can inhibit and retard cancer -Modulated 0.5 Hz and 16.5 Hz produced a pronounced antitumor effect and inhibited or suppressed the growth of Ehrlich ascites carcinoma (EAC) in mice.The maximum effects occured at 100 and 300 nT at a frequency of 4.4 Hz.The necrosis was prevailing type of cell death (Novikov, 2005, 2009).-A low-intensity frequency-modulated (25 -6 Hz) EMF pattern daily, 1 h, exposures inhibited the growth of malignant cell lines, and HeLa cells but did not but did not affect the growth of non-malignant cells (Buckner, 2015).1.6) Mhz and GHz EM frequencies located in coherent zones can inhibit and retard cancer -Pulsed electric fields of of 0.5 Hz and greater than 20 kV/cm, with rise times of 30 ns and durations of 300 ns (3.32 MHz) penetrate into the interior of tumor cells and cause tumor cell nuclei to rapidly shrink and tumor blood flow to stop.Melanomas shrink by 90% within two weeks.A second treatment at this time can result in complete remission (2006).
induce tumor regression in vivo: a total of 200 pulses of 20 ns duration at 25 kV/cm led to an 84% decrease in viable cells compared to controls.A total of 200 pulses of 20 ns duration at 35 kV/cm caused complete eradication of the cells (Garon, 2007).-Nanosecond pulsed electric fields (nsPEFs) can affect the intracellular structures of cells in vitro.This study shows the direct effects of nsPEFs on tumor growth, tumor volume, and histological characteristics of normal skin and B16-F10 melanoma in SKH-1 mice.A melanoma model was set up by injecting B16-F10 into female SKH-1 mice.After a 100-pulse treatment with an nsPEF (40-kV/cm field strength; 300-ns duration; 30-ns rise time; 2-Hz repetition rate), tumor growth and histology were studied.After nsPEF treatment, tumor development was inhibited with decreased volumes post-nsPEF treatment compared with control tumors (P < 0.05) (Chen XR, 2009).
development of brain cancer by inhibiting the cytochrome c/caspase-3 apoptotic pathway (Leszczynski 2002).-Exposure of rats by a combination of a continuous wave form in a nearby coherent zone at a low exposure level does not affect tumor growth.Low-level exposure of mammary-tumor-prone mice to 2450 MHz RFR circularly polarized waveguides (CWG) for 18 months (20 h/day, 7 days/wk) to continuous-wave 2450 MHz RFR at a whole body average specific absorption rate (SAR) of 0.3 W/kg did not affect mammary tumor incidence, latency to tumor onset, tumor growth rate, or animal longevity when compared with sham-irradiated controls (Frei, 1998).
experimentally in hairless mice; this action spectrum shows a peak at 293 nm in the UV-B range (DeGruijl et al., 1993).1.10) Mhz and GHz frequencies located in coherent zones with estimated modulations in non-coherent zones can cause cancer -A high frequency 900 MHz signal located in a coherent zone at a low SAR of 0.13 -1.4 W/kg, modulated with estimated incoherent frequencies in the decoherent soliton frequency-zone, can cause cancer after 2 years exposure in animals (Repacholi, 1997).-Ahigh frequency signal at a high SAR of at least 5.0 W/kg caused DNA damage (strand breaks/alkali labile sites) in leukocytes using the alkaline (pH > 13) single cell gel electrophoresis (SCG) assay in vitro studies of modulated 837 and 1909.8MHz exposed human blood leukocytes and lymphocytes.This demonstrates that, this kind of EMF is capable of inducing chromosomal damage in human lymphocytes (Tice, 2002).-Highfrequency signals of 900 and 1900 MHz located in a coherent zone, and modulated with estimated incoherent frequencies in the decoherent soliton frequency-zone at a high SAR of 6 W/kg during an exposure of 2 years can show schwannomas in the heart of male rats (Wyde et al., 2016).

1. 11 )
Mhz and GHz EM frequencies located in decoherent zones with estimated modulations in non-coherent zones can cause cancer at a lower exposure level -Expose mice to modulated 9270 MHz waves can causes cancer (Prausnitz D. K. F. Meijer, H. J. H. Geesink DOI: 10.4236/jct.2018.93019227 Journal of Cancer Therapy and Susskind, 1962).Rat exposed to pulsed 2450 MHz at 0.48 mW/cm 2 and at SARs up to 0.4 W/Kg, 21.5 hr/day, 7 days/wk, 25 month show that carcinomas are increased and malignant tumors of endocrine and exocrine organs as a group are increased (Guy et al. 1983, 1985).

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Based on mesoscopic modelling of DNA breathing dynamics in a THz field, it has been suggested that THz radiation may amplify existing (or create new) open states in the double helix, thereby affecting transcription initiation or binding of transcription factors and influences of terahertz radiation effect on gene expression in mouse mesenchymal stem cells (Alexandrov, 2010, 2013).Appendix 2. Databank for reported EM frequencies of the analyzed biological studies.
[99]/kg.A second technology might be the application of so called trans-material catalysts[99]that are nano-and micron semiconductors able to add preferred coherent condensate signals to electromagnetic man made signals.
broblasts.Microwave fields, amplitude modulated (AM) by an extremely low-frequency (ELF) sine wave, induced a nearly twofold enhancement in the activity of ornithine decarboxylase (ODC) in L929 cells at SAR levels of the or-D.K. F. Meijer, H. J. H. Geesink DOI: 10.4236/jct.2018.93019201 Journal of Cancer Therapy der of 2or even may be technically integrated in the many other electronic devices in daily practice, in order to create a healthy EM environment in the vicinity of our body [13] [118] [119] [120] [121].
, H. J. H. Geesink DOI: 10.4236/jct.2018.93019205 Journal of Cancer Therapy frequency as well as wave forms, ranging from sinusoidal to square-wave to pulsed-wave forms across studies.Baharara et al. showed that extremely low EMF therapy restored the sensitivity of cisplatin resistant human ovarian carcinoma cells by increased apoptosis rates.In combination with radi- Meijer, H. J. H. Geesink DOI: 10.4236/jct.2018.93019206 Journal of Cancer Therapy direction and NsPEF, at 100 ns pulses(10 MHz)in duration and 20 kV/cm in intensity applied at a frequency of 0.5 Hz, could inactivate metastasis and invasion in cancer cells by suppressing Wnt/β-Catenin signaling pathway to down-regulating expressions of VEGF and MMPs family proteins.It is found that nsPEF in-