Radio
Frequency (RF electromagnetic) Cancer Causation and Cure opening our Minds not
closing our Hearts, by Dr Chris Barnes, Bangor Scientific and
Educational Consultants, First Released into public domain in Beta form with no
full reference list 4th January 2017. E-mail
manager@bsec-wales.co.uk
Short
Abstract
In this
paper I re-evaluate Geesink’s bio
–soliton Clathrate RNA replicator hypothesis and how its links with both the
primordial and modern day electromagnetic spectrum. I show perfect matches between Earth’s
Schumann Resonance frequencies and Jovian Frequencies and Geesink’s
condensates. Armed with this knowledge and re-evaluating what is known about the
way certain radio frequencies disturb life processes as a result of a very huge number of studies,
some occupational epidemiology, some TV/Radio antenna geospatial studies, some
in vivo animal studies and some in vitro cell culture studies , has led me directly to the discovery of my own set
of cancer treating frequencies (patents applied for) which almost miraculously
appear to be able to replicate the modus operands of several different classes
of cancer tumour treating drug. Depending on specific frequency
condensates related with Geesink’s THZ RNA replicator frequencies treatments
can be expected to be achieved at least equivalent to the following classes of
cancer drug: Cell cycle Modulators,
Calcium channel Blockers, ATP inhibitors, ROS modulators and tubulin
polymerisation inhibitors. Further I
also believe I can now also fully explain the cancer treating frequencies which
have been used in an almost hap hazard manner by other groups previously only
on the basis of obscure pulse rate
biofeedback selection.
Long
Abstract
This paper supplies logical proof of the chain of physical mechanisms involved
in the hitherto not understood subtle field anti-cancer process.
Rife’s 1930’s RF microbe and cancer destruction
technology is presented and discussed.
Kirson (2007) also showed that similar fields inhibit by an
anti-microtubule mechanism of action i.e. disruption of the mitotic spindle,
cancerous cell growth in vitro. The
spindle consists inter-alia of microtubules, electrically polar structures
fulfilling Pohl’s prediction as
prerequisites for generation of coherent
oscillatory electric fields in the kHz to GHz region. Ephram concludes there is Limited Evidence of
RF fields being Genotoxic at least from In-Vitro studies.
Adair (20030
acknowledges that energies of greater than KT could be reached for dielectric
absorption into large free single cells of radius greater than 20 microns. Further, that energies approximating KT could
be dumped into Biological systems at E FIELD strengths exceeding 200volt /metre. I raise additional mechanisms whereby
non-thermal, non-ionising radiation can influence biological systems and cancer
aetiology and provide hitherto non –established links and cite a catalogue of others’ experimental evidence constructed in
logical progression to form complete
and fully explainable experimentally
tested and further future testable
pathways for the influence of RF on
mutations with regard to cancer causation and progression and
additionally with regard to the mitotic
spindle and tubulin polymerisation as a mode of cancer suppression. All this notwithstanding possible effects
of RF on the immune system and T-cell
populations.
It has long been established that dividing yeast
cells emit bio fields. Further it is
established there is a biological electric field gradient across wounded, cut
or damaged tissue. The fact that
bio-electromagnetic fields exist suggests that they ought to be able to
be coupled to or influenced by external influence. A recent
paper by Havas (2016)
attempts to resolve the debate about whether non-ionizing radiation
(NIR) can cause cancer–a debate that has been ongoing for decades. The
rationale, put forward mostly by physicists and accepted by many health
agencies, is that, “since NIR does not have enough energy to dislodge
electrons, it is unable to cause cancer.” This argument is based on a flawed
assumption and uses the model of ionizing radiation (IR) to explain NIR, which
is inappropriate. Evidence of free-radical damage has been repeatedly documented
among humans, animals, plants and microorganisms for both extremely low
frequency (ELF) electromagnetic fields (EMF) and for radio frequency (RF)
radiation, neither of which is ionizing. While IR directly damages DNA, NIR
interferes with the oxidative repair mechanisms resulting in oxidative stress,
damage to cellular components including DNA, and damage to cellular processes
leading to cancer. Furthermore, free-radical damage (ROS) explains the
increased cancer risks associated with mobile phone use, occupational exposure
to NIR (ELF EMF and RFR), and residential exposure to power lines and RF
transmitters including mobile phones, cell phone base stations, broadcast
antennas, and radar installations. This is in strong support of my earlier work
(2014).
Critically and as I proposed, other experimental
results indicate the differences in dynamics of ultra-weak photon emission
between cells exposed to magnetic field and controls cells. Ion cyclotron
resonance predicts a resonant response
of the bio-system to the magnetic field results also measured experimentally.
Caligiuri has shown that Microtubule assembly is regulated by Ca2+-loaded
calmodulin. Thus we now have a direct link between RF input, Calcium ion
movement and staging of the microtubule
assembly.
Some modern chemotherapy agents are tubulin
polymerization disruptors. It is shown that
electromagnetic absorption can achieve the same means to an end, thereby
completing a complete physical picture and mechanism whereby subtle field/
subtle modulation cancer treatment
systems actually work.
We can now begin to see why there should be
exposure time, amplitude and frequency critical domains in different tissue and
tumour types. For example some types of
cancer cells are more acidic than normal cells, see Griffiths 1991 and Stubbs
(2000). Stubbs comments that the acidic
environment may lead to new treatment strategies. Certainly it will lead to different ion gradients and hence
different cyclotron resonance frequencies.
Likewise there will be different
micro-environment for the mitotic spindle, different mechanical properties and
stiffness and hence different
resonance frequencies. Here and thus I propose this elegantly
explains the hitherto totally
unexplained observations of Barbault et al (2009). Resonance effects disrupting the mitotic
spindle either by direct mechanical disturbance
and/or via effects of cyclotron resonance on calcium ions. Polymerisation
of tubulin is thus prevented so the cell
cycle is halted and proliferation can no longer occur. Because tumour cell microenvironments and
their cellular stiffness is different by cell line type, a different set of
treatment frequencies is to be expected for each cancer type and healthy cells
will be unaffected. This is exactly as
is observed by Barbault et al (2009).
Now that I have provided a proper physical basis for Barbault’s work I
would hope these types of technology will be thoroughly and quickly developed
to the benefit of all human kind. There is also no reason to suppose spin –offs
for treating animal cancers will not be possible also. The icing on the cake
comes with the present author’s re-evaluation of Geesink’s bio –soliton
Clathrate RNA replicator hypothesis and its links with both the primordial and modern
day electromagnetic spectrum. This leads
directly to the discovery of my own set of cancer treating frequencies (
patents applied for) which almost miraculously appear to be able to replicate
the modus operands of several different classes of tumour treating drug.
Introduction
The present author has published previously and
extensively on the epidemiology, hazards and mechanisms of RF
radiation with respect to cancer
incidence and potential modes of
causation. Because only about 50% of the
very diverse works in the field to date necessarily conclude that RF
radiation is hazardous, this has led
to a range of misinformed and
even sceptical conclusion. Those adjudging ranging from those who conclude that RF is completely safe to those who
wholly dismiss any RF interaction whatsoever with biology. This
is despite the fact that one cannot escape, for example, the fundamental
Physics of dielectric absorption and displacement current in materials (Gabriel
et al 1996)[1] . Let alone before one even starts to consider
more complex concepts such as Frolich’s coherent vibrations( Frolich 1968) [2]. Such scepticism is in the author’s
view clearly that of people with closed
hearts and minds and such opinion has,
also from the authors’ viewpoint,
hindered the development of new RF based
technologies for treating/curing cancer.
Applying a little lateral thinking is useful. For instance if 50% of RF interactions with
biology are negative there is just as much chance of the other 50% being
positive than neutral or non –reactions.
One doesn’t have to look very far in the scientific literature to find
positive instances such as pulsed electromagnetic bone healing and the like,
see for example but by no means exclusively, Basset 1989[3]. Then there are the
reports which deal with changes in RF cancer thermotherapy strategy over the
years and the evidence therein that
switching from ablation at 49C
down to ablation at 42C improved survival and prognosis, perhaps suggesting
some non –thermal or coherent cytotoxic effects were taking place?
Most importantly,
I will attempt to show that
recently reported experimental results, E.G. those of, for example,
Barbault et al (2009) [4] using non-ionising, non-thermal RF radiation
to prolong the lives of terminal cancer patients together with in vitro
conformation of effect and the eventual
the eventual feasibility to treat
and cure cancer with subtle
field RF ( as opposed to thermal
ablation methods ) is actually fully and
directly supported by the above mentioned diverse range of observation
with regard to causation to date.
Moreover in this paper I will attempt to supply logical proof of the chain of physical mechanisms involved
in the subtle field anti-cancer process.
I would
ultimately envision a device not
that unlike Star Trek’s
‘Tricorder’. Indeed, such a device
was close to possibly close to realisation in the 1930’s, the so called Rife
Machine. Rife claimed that cancer was
caused by an two unknown microbes. Microbes covers bacteria, viruses and
fungi. Indeed in more than one respect
he was essentially correct. Firstly, the bacterium H-pylori is undisputedly associated with
gastric cancer. Secondly, Human
papilloma virus is indisputably
associated with cancer. Most cancers of the vagina and anus are likewise
caused by HPV, as are a fraction of cancers of the vulva, penis, and
oropharynx. HPV-16 and -18 account for about 70% of cancers of the cervix,
vagina, and anus and for about 30–40% of cancers of the vulva, penis, and
oropharynx. Other cancers causally linked to HPV are non-melanoma skin cancer
and cancer of the conjunctiva, see Munoz et al (2006) [5].
Finally
systemic candida ( fungi) infection is found in a significant number of cancer
patients, see for example, but not exclusively, Maksimiuk (1984) [6] and many other similar
references! Rife claimed his machine which used a carrier frequency of 3.3 MHz and
multiple KHz A.M. modulation frequencies could kill a number of bacteria and
viruses including the ones allegedly causing cancer. Rife could use his machine either with a
special microscope where he claimed he could observe bacterial death or in
close proximity with human subjects. The
machine produced about 50 watts of RF carrier wave coupled into a gas filled
plasma tube ‘antenna’. Early pictures of
the antenna show it glowing violet in colour.
My guess is that, despite many claims to the contrary by contemporary
‘lay’ websites, such tubes would emit a
certain quantity of UV light. With regards to killing bacteria and viruses on
the microscope slide, UV light is potent, as evidenced by its use in modern
water and sewage treatment. However, it
is less likely how it influenced patients unless it perhaps after several hours
use increased serum vitamin D? Other than that one can only assume there was something in the
interaction of the subtle sets of frequencies which Rife’s machine
supplied. Problematically, however,
since then various machines similar to Rife’s have been made but with unscrupulous
operators claiming cure-alls for all manner of ills. Thus Rife technology
quickly fell into the realms of quackery.
It is perhaps somewhat surprising then
to learn that not totally
unrelated systems in that it has a low power HF carrier wave and is AM
modulated has recently been used for
experimental Cancer Treatment e.g. ‘Amplitude-modulated electromagnetic fields
for the treatment of cancer: Discovery of tumor-specific frequencies and
assessment of a novel therapeutic approach’
see Barbault et al (2009)[4] and further related work reported in a respected journal, the
Journal of Cancer, ‘Treatment of
advanced hepatocellular carcinoma with very low levels of amplitude-modulated
electromagnetic fields’ see Costa et al ( 2011)[7]. Zimmermann et al (2011) [8] designed and used an in vitro cell culture system and
successfully duplicated the effects seen in Costa’s in vivo study. Maybe Rife’s machine wasn’t quackery
after all? For instance Giladi et al
(2008) [9] showed that weak
electric currents generated using conductive electrodes increased the efficacy
of antibiotics against bacterial biofilms, a phenomenon termed “the bioelectric
effect.” They inhibited the growth of
planktonic Staphylococcus aureus and Pseudomonas aeruginosa in an amplitude and frequency dependent manner,
with a maximum at 10 MHz
Kirson (2007) [10 ] showed that low intensity,
intermediate frequency, electric fields inhibit by an anti-microtubule
mechanism of action i.e. disruption of the mitotic spindle, cancerous cell
growth in vitro. Using implanted electrodes, these fields were also shown to
inhibit the growth of dermal tumours in mice.
Although Pasche of Costa’s research team does not know the ‘biophysical
mechanism he too has seen disruption of the mitotic spindle. Kirson’s earlier work ( 2004) may give
further mechanistic clues.
Low-intensity, intermediate-frequency (100–300 kHz), alternating
electric fields, delivered by means of insulated electrodes, were found to have
a profound inhibitory effect on the growth rate of a variety of human and
rodent tumor cell lines (Patricia C, U-118, U-87, H-1299, MDA231, PC3, B16F1,
F-98, C-6, RG2, and CT-26) and malignant tumors in animals. This effect, shown
to be nonthermal, selectively affects dividing cells while quiescent cells are
left intact. These fields were said to
act in two modes: arrest of cell proliferation and destruction of cells while
undergoing division. Both effects were demonstrated when such fields are
applied for 24 h to cells undergoing mitosis that is oriented roughly along the field direction. The
first mode of action is manifested by interference with the proper formation of
the mitotic spindle, whereas the second results in rapid disintegration of the
dividing cells. Both effects, which are frequency dependent, are consistent
with the computed directional forces exerted by these specific fields on
charges and dipoles within the dividing cells. In vivo treatment of tumors in
C57BL/6 and BALB/c mice (B16F1 and CT-26 syngeneic tumor models, respectively),
resulted in significant slowing of tumor growth and extensive destruction of
tumor cells within 3–6 days. Their findings demonstrated the potential
applicability electric fields as a novel therapeutic modality for malignant tumors. In fact
dividing cells ( yeast cells ) have also been shown to give out their own RF emissions. Jelonek et al
(1999) measured electromagnetic signals in the frequency range from 8 to 9 MHz
are compared with evolution of the reassembled microtubules. They detected
signals peak in the time interval 25–30 min and 45–60 min after the release of
the cells from the restrictive to the permissive temperature. The first maximum
corresponds to the stage when the mitotic spindle is formed and binds chromatids.
The second maximum is measured when the processes of anaphase A and of anaphase
B take place.
Cifra and Pokorny (2009)[11] confirmed the presence of electromagnetic emissions from dividing
yeast cells in terms of mechanical vibrations of polar structures. Electromagnetic
activity around yeast mitotic cells (Saccharomyces cerevisiae) was measured in
the same frequency range 8–9 MHz and special care was taken to extract reliable
information from the raw signals. The characteristic of cold-sensitive tubulin
mutants tub2-401 and tub2-406, which come to arrest before mitosis at a
restrictive temperature (14°C) and which re-enter mitosis upon a shift back to
a permissive temperature (28°C), was used to prepare synchronized mitotic
cells. Immunofluorescence microscopy using an antitubulin antibody was used to
analyze microtubular structures. The arrested tub2-401 mutant that had
back-shifted to permissive temperature displayed no microtubules and no
electromagnetic activity around the cells. In contrast, the arrested cells of
the mutant tub2-406 displayed developed, but aberrant, nonfunctional
microtubules and a high electromagnetic activity around the cells. The
electromagnetic activity around the arrested mutant tub2-401 back-shifted to
permissive temperature peaks at four time points which may coincide with (i)
formation of the mitotic spindle, (ii) binding of chromatids to kinetochore
microtubules, (iii) elongation of the spindle in anaphase A, and (iv)
elongation of the spindle in anaphase B. The profile of the electromagnetic
activity around the synchronized mutant tub2-406 at permissive temperature
seems to be delayed by the time required for aberrant nonfunctional
microtubules to be depolymerized. Experimental results presented in their paper
supported Pohl's idea of existence of the electromagnetic field around yeast
cells.
Microtubules are electrically polar structures
fulfilling prerequisites for generation of oscillatory electric field in the
kHz to GHz region, see Cifra et al 2010 [12]. Energy supply for excitation of
elasto-electrical vibrations in microtubules may be provided from
GTP-hydrolysis; motor protein–microtubule interactions; and energy efflux from
mitochondria. Little wonder then that externally applied RF disturbs this
process. Experimental results presented
in this manner support the great late theoretical Physicist Herbert
Pohl's (whom I met personally in the late 1970’s) idea of existence of the
electromagnetic field around living cells.
Not just human tissue is affected by RF , for
example, Tkalec et al (2009) [13]
considered plants ‘Effects of
radiofrequency electromagnetic fields on seed germination and root meristematic
cells of Allium cepa L.’ They observed effects
which were markedly dependent on the field frequencies applied as well
as on field strength and modulation. Their findings also indicate that mitotic
effects of RF-EMF could be due to impairment of the mitotic spindle. Priel et al (2006) [14 ]
have shown microtubules, the building blocks of the mitotic spindle to act as
biopolymer transistors capable of electrical
amplification. Small wonder then that subtle field effects are found in
biology.
There is perhaps no more emotive a topic in modern
science than the one this discussion
paper attempts to deal with, that is, can anthropogenic sources of radio
frequency radiation contribute in some way to modern cancer aetiology be it
either with regard to causation or manipulation to open up a possible cure-all? The present author or has asked himself why,
particularly with regard to cancer causation,
is this topic so emotive. Perhaps the answer lies in the fact that we
are all exposed to a multiplicity of RF energies, frequencies and modulation
schemes on a daily and life-long basis.
‘Joe public’, who may necessarily have no Physics Biology or Engineering training is forced to ‘Google’ the topic and either
hits on a site funded by a scaremonger
group or a site funded by a mobile phone company, the former telling Joe he is
doomed to death hell and destruction,
the latter telling him not only is his phone totally harmless but that it may
even also improve his memory.
Then Joe has to visit the ‘Forum’s where he might
meet the real nasty guys. I didn’t write
a review paper here because some of the stuff published on this topic states
the unbelievable. One recent article I
read suggested that because we don’t know all the mechanisms
involved let’s not bother with any more studies. How in God’s name is that
Science?
To reinforce my point, I turn to the human
ear. We can hear but we still don’t know
the precise mechanism of the cochlear amplifier, so let’s all go deaf. The
point I am making here is that this hasn’t prevented the development of the
traditional hearing aid or even the cochlear implant!
Let’s take Joe back to the forum. There recently I met a guy, let’s call him Mr
X who stated ‘RF can’t interact with
living cells because its wavelength is
too big and there is no way of focusing it.
Well perhaps our Mr ‘X’ Forum expert would like to go back and look at
the ear again. So for a 330 Hz tone he’s have me with a 1-metre-wide aural
canal, no doubt? Trust me if Mr X had
ever had the author’s experience RF burns to fingers and thumbs or felt the
inside of his chest wall getting hotter than its surroundings in the near field
of an HF transmitting antenna he would have doubts whatsoever that RF could
interact with living tissue!
What concerns us here however, is not thermal
effect but non-thermal effects or so called subtle -field effects and
ultimately how we will utilise them to the benefit of human kind.
Further, what this paper will not attempt to be is
a review paper. Quite simply there are so many thousands, if not tens of
thousands of published works in the dual fields of electromagnetic cancer
causation and treatment.
Dealing firstly with some of the more significant
works on cancer causation these can be divided briefly into areas which are:
1.
In vitro
cellular and DNA studies
2.
In vivo
animal studies
3.
Specific
group epidemiological studies
4.
Wider population epidemiological studies
The situation is further complicated because strictly
RF or electromagnetic radiation covers the complete spectrum of frequency from
DC through to Gamma radiation.
There is, however, a certain logic in this
limitation. For example, the
National Cancer Institute finds a paper,
by Kliukiene et al, Epidemiol. 2004 May
1;159(9):852-61[15] , ‘Residential
and occupational exposures to 50-Hz magnetic fields and breast cancer in women:
a population-based study,’ to be statistically relevant
Those authors conducted a case-control study to
investigate whether residential and occupational exposures to magnetic fields
increased the risk for breast cancer among women. Cases of breast cancer
diagnosed during 1980-1996 were identified in a cohort of women living near a
high-voltage power line in Norway in 1980 or between 1986 and 1996. Each case
was matched by year of birth, municipality, and first year of entry into the
cohort with two randomly selected controls without cancer. Residential exposure
to magnetic fields was calculated as that generated by the lines before
diagnosis, and occupational exposure was based on exposure matrix data. Women
with residential exposure had an odds ratio of 1.58 (95% confidence interval
(CI): 1.30, 1.92) when compared with unexposed women. The odds ratios for
exposed women versus unexposed women with estrogen receptor (ER)-positive and
ER-negative breast cancer were 1.33 (95% CI: 0.93, 1.90) and 1.40 (95% CI:
0.78, 2.50), respectively (ER status was available for 44% of the cases). Women
with the highest occupational exposure had an odds ratio of 1.13 (95% CI: 0.91,
1.40) when compared with those unexposed at work. At first sight, their
findings suggest a definite and statistically relevant association between
exposure to magnetic fields and breast cancer in women.
However, at power line frequencies 50/60 Hz other factors such as
concentration of radon and airborne pollution by the electric fields overhead
high voltage cables may cloud the issue. In a similar vein, I have previously
shown how the changeover from CRT to LED TV sets reduced cancer rates, the
former being a similar concentrator of radon and household airborne pollutants,
see my paper viewing and cancer, the
enemy in your front room, a television hypothesis revisited, expanded and
slightly revised. By Dr Chris Barnes Bangor Scientific and Educational Consultants March
2015. E-mail manager@bsec-wales.co.uk wherein
interestingly I was also able to separate out the excess cancer risk of CRT’s
from RF radiation in the UK since 1947.
At the
other end of the spectrum, optical frequencies and beyond have flux quanta
energetic enough to cause electronic transitions and to directly perturb
chemical bonds wherein bio-effect would likely never be questioned by anyone.
Thus for the remaining purposes of the present
discussion there have been shown good reasons to limit our frequency range from
say KHz frequencies to microwave frequencies say of 90 GHz or so, this range is
often referred to as non-ionising radiation. So indeed, if we limit ourselves to this range in
question, roughly, what are the results?
Several recent review papers reach different
conclusions on the overall risk of RF radiation. Thus perhaps it is better to
consider looking at the conclusions of scientific bodies and panels charged
with looking after public safety?
One such body is EPHRAN (the European body for
assessing Health Risks of RF radiation)
The Ephran
Classification Definitions are shown below
Further shown below are the Ephran conclusions,
especially with regard to Genotoxicity ( Cancer Studies)
We can see that Ephram concludes there is Limited
Evidence of RF fields being Genotoxic at least from In-Vitro studies.
Ephram does not discuss workplace or population at
large epidemiology in detail but the National Cancer Institute do. Mixed
results are obtained. With workplace exposures to radiofrequency radiation. A
limited number of studies have evaluated risks of cancer in workers exposed to
radiofrequency radiation. A large study of U.S. Navy personnel found no excess
of brain tumors among those with a high probability of exposure to radar
(including electronics technicians, aviation technicians, and fire control
technicians); however, nonlymphocytic leukemia, particularly acute myeloid
leukemia, was increased in electronics technicians in aviation squadrons, but
not in Navy personnel in the other job categories. A case-control study among
U.S. Air Force personnel found the suggestion of an increased risk of brain
cancer among personnel who maintained or repaired radiofrequency or
microwave-emitting equipment. A case-control study found the suggestion of an
increased risk of death from brain cancer among men occupationally exposed to
microwave and/or radiofrequency radiation, with all of the excess risk among
workers in electrical and electronics jobs involving design, manufacture,
repair, or installation of electrical or electronics equipment. There was no
evidence that electrical utility workers who were exposed to pulsed
electromagnetic fields produced by power lines were more likely to develop
brain tumors or leukemia than the general population. Employees of a large
manufacturer of wireless communication products were not more likely to die from
brain tumors or cancers of the hematopoietic or lymphatic system than the
general population.
There are few epidemiologic studies dealing with
electromagnetic radiation and uveal melanoma. The majority of these studies are
exploratory and are based on job and industry titles only. Stang et al (2001) [16] conducted a hospital-based and
population-based case-control study of uveal melanoma and occupational
exposures to different sources of electromagnetic radiation, including radiofrequency
radiation. They then pooled these results. They
interviewed a total of 118 female and male cases with uveal melanoma and
475 controls matching on sex, age, and study regions. Exposure to
radiofrequency-transmitting devices was rated as (a) no radiofrequency
radiation exposure, (b) possible exposure to mobile phones, or (c)
probable/certain exposure to mobile phones. Exposures were rated independently
by two of the authors who did not know case or control status. They used conditional logistic regression to
calculate odds ratios (ORs) and 95% confidence intervals (95% CIs). They found an elevated risk for exposure to
radiofrequency-transmitting devices (exposure to radio sets, OR = 3.0, 95% CI =
1.4–6.3; probable/certain exposure to mobile phones, OR = 4.2, 95% CI =
1.2–14.5). Their study was the first describing an association
between radiofrequency radiation exposure and uveal melanoma.
Human populations are increasingly exposed to
microwave/radiofrequency (RF) emissions from wireless communication technology,
including mobile phones and their base stations. By searching PubMed, Khurana
et al (2010) [17] identified a total
of 10 epidemiological studies that assessed for putative health effects of
mobile phone base stations. Seven of these studies explored the association
between base station proximity and neurobehavioral effects and three
investigated cancer. They found that eight of the 10 studies reported
increased prevalence of adverse neurobehavioral symptoms or cancer in populations
living at distances < 500 meters from base stations. None of the studies
reported exposure above accepted international guidelines, suggesting that
current guidelines may be inadequate in protecting the health of human
populations. They believe that comprehensive
epidemiological studies of long-term mobile phone base station exposure are
urgently required to more definitively understand its health impact.
Mechanisms
Adair (2003) and Challis (2005) appear to be the only two authors who have
theorised that non –ionising, non-thermal
RF radiation of the order of 10mW/cm^2 will not influence biology
significantly on the basis that energy imparted ( excluding sharp resonance
effects) will be less than random thermal energy ( kT). However, Adair
does acknowledge that energies of greater than KT could be reached for
dielectric absorption into large free single cells of radius greater than 20
microns. Further that energies
approximating KT could be dumped into Biological systems at E FIELD strengths
exceeding 200volt /metre. Returning to my example of the ear is of
course instructive here. One would,
hopefully, assume Adair and Challis
are aware of its basic
physiologically and perhaps also the
work of Denk and Webb (1989)[18] who
show that hair cells in the cochlear
reach the sensitivity limit imposed by the thermal noise at their
input. If one part of biology is
capable of such a refinement there is perhaps no reason to suggest that the
important processes of cell division and
differentiation could not be equally refined. It is my guess that the sceptics I refer to
hereinabove and probably the mobile phone and other communications operators
who seek to re-assure their customers have looked no further than and only briefly at Adair and Challis. A return to the ear for comparison has been
shown to be instructive. And, of course
there are other examples of remarkable environmental sensitivity operating at
or even less than the ‘KT’ limit throughout the animal kingdom.
In the rest
of this paper I pose the question, ‘did Adair and Challis look deeply enough
into the problem at hand?’ I raise
additional mechanisms whereby non-thermal, non-ionising radiation can influence
biological systems and cancer ethology and provide hitherto non –established
links and attempt to cite a catalogue
of others’ experimental evidence in
logical progression to form complete and
fully explainable experimentally tested
and further future testable pathways
particularly for the influence of RF on
mutations with regard to cancer causation and progression and with
regard to the mitotic spindle and
tubulin polymerisation as a mode of cancer suppression. All this notwithstanding possible effects
of RF on the immune system and T-cell
populations, see for example Lauer [19]. http://www.vincent-lauer.fr/cancer-autoimmunity.pdf
RF and
free radicals in Biology
In 2014 I published an online paper entitled ‘The unified missing link, oxidative
stress as a result of altered
water structure at gas -liquid interfaces leading to apparent
electromagnetic memory and accounting
for very diverse instances of radio frequency induced plant and animal
bio-damage such as Tree Die- back, Cancers and even Stroke’ [20] . I briefly discussed
safety concerns of RF radiation and explained how some
literature suggests that RF could be either a carcinogen or a cancer promoter. I concluded that the need to take the quantum
mechanical aspects of radio propagation into account together with the
compounding effects of atmospheric pollution and other carcinogens is once
again highlighted. An observation that
not only cancer and tree damage may be caused by RF was highlighted, but also
there is the possibility of it being implicated in increased stroke risk in
15-44 year olds. I formulated a new model based on the perturbation of the balance of natural biological free radical reaction
processes by RF at gas-liquid interfaces is developed. The model accounts elegantly for a
significant number of effects of RF including changes in calcium channel
behaviour, dominance of association with cancers of the blood and lymphatic
systems, damage to trees and plants and even the seemingly new and high prevalence
of stroke in the younger age groups who are more likely to be engaging with
mobile and WIFI RF technologies. The
model is strongly supported by existing experimental evidence in a number of
related physical and life science fields.
I further concluded that RF even at very low levels may prove to be an
additional lifestyle risk factor rather like smoking or alcohol. Due
to the long half-lives of altered water structure in the presence of micro and
nano-gas bubbles medium term exposure, such as sleeping in elevated levels of
RF, may be as or more dangerous than occasional exposure to very high levels. Intriguingly, Lauer too reaches this
conclusion and beyond, citing rare mobile phone use as anti-cancer and regular
mobile phone use as pro-cancer [19].
A recent
paper by Havas (2016) [21] attempts to resolve the debate about whether non-ionizing
radiation (NIR) can cause cancer–a debate that has been ongoing for decades.
The rationale, put forward mostly by physicists and accepted by many health
agencies, is that, “since NIR does not have enough energy to dislodge
electrons, it is unable to cause cancer.” This argument is based on a flawed
assumption and uses the model of ionizing radiation (IR) to explain NIR, which
is inappropriate. Evidence of free-radical damage has been repeatedly
documented among humans, animals, plants and microorganisms for both extremely
low frequency (ELF) electromagnetic fields (EMF) and for radio frequency (RF)
radiation, neither of which is ionizing. While IR directly damages DNA, NIR
interferes with the oxidative repair mechanisms resulting in oxidative stress,
damage to cellular components including DNA, and damage to cellular processes
leading to cancer. Furthermore, free-radical damage (ROS) explains the
increased cancer risks associated with mobile phone use, occupational exposure
to NIR (ELF EMF and RFR), and residential exposure to power lines and RF
transmitters including mobile phones, cell phone base stations, broadcast
antennas, and radar installations.
Clearly, Havas’ paper is in strong support of my work.
ROS has recently been shown also to be relevant in
cancer treatment as cancer cells do not extinguish free radicals as quickly as
healthy cells. High levels of ROS could therefore kill cancerous tumour cells. Traditional radio (isotope) therapy and
possibly ultrasound therapy produce large quantises of free radicals. Recently in RF thermotherapy there has been a
shift from very high temperature ablation ( up to 49 C ) down to more moderate temperatures of some
42 C without noticeable change in the effectiveness of treatment. Maybe the answer in in ROS generation. Mustafa et al [22] using Iron oxide nanoparticle-based
radio-frequency thermotherapy for human breast adenocarcinoma cancer
cells. Iron oxide nanoparticles (IONPs)
with diameters of 15, 25, and 41 nm were evaluated as mediators of thermal
cytotoxicity under radio-frequency (RF) exposure. The 25 nm IONPs were found to
be the most efficient of the three in killing cancer cells at 350 kHz
low-frequency RF irradiation. However, at a higher frequency of 13.56 MHz, 15
nm IONPs produced the highest percentage of cell death. Moreover, the killing
effect was concentration-dependent in that a higher concentration of IONPs
resulted in increased cellular death. Size-dependent internalization of IONPs
in MCF-7 cells was quantified by using inductively coupled-plasma mass
spectrometry (ICP-MS). Dark-field microscopy and transmission electron
microscopy (TEM) revealed that MCF-7 cells internalize IONPs through
endocytosis after 24 hours of incubation. In addition, after RF treatment, the
cancer cells underwent the apoptosis process, and the level of reactive oxygen
species (ROS) increased significantly after hyperthermia. Scanning electron
microscopy (SEM) and TEM further established that the ultrastructure
morphological changes in the cancer cells originated from the apoptosis
process. Honda et al (2004) have also brought about apoptosis induced by
ultrasound and conclude that Calcium ions and ROS are involved. Mitotic catastrophe (MC) is a sequence of
events resulting from premature or inappropriate entry of cells into mitosis
that can be caused by chemical or physical stresses. There are several
observations permitting to define MC as an oncosuppressive mechanism. MC can
end up in apoptosis, necrosis or senescence.
Some cancer drugs such as doxorubicin-induce apoptosis which is
ROS-dependent.
As I have shown previously (Barnes 2014) ROS
there is a perfectly feasible mechanism whereby ROS can be generated by low
level ( subtle field) RF radiation and thus this alone may explain some of the
anti-cancer effects of the Rife machine and similar modern versions of the technology.
Added
tiers of complexity: information
Clearly, not all whole body exposures to RF
radiation result in cancer tumourogenisis,
promotion or suppression. Likewise only about half of the 5000 or so
in vitro experiments with mobile phone and other frequencies of RF emission
have produced any results. This is to
be expected in terms of exposure times and random chance just as with exposure
to chemical carcinogens.
In terms of
geo-spatial epidemiology, I have already showed it is the transmission
of information ( modulation) into the body or its cells that is crucial and I
have produced a quantum mechanical model
[23] to explain this
regarding imprinting of information into biological systems which successfully
accounts for the distribution of cancer clusters at certain key distances from
transmitting antennas such as those of TV towers and mobile phone installations.
Further, the same model successfully
predicts bio-damage to trees. Further
RF bio-damage to trees and humans is
enhanced significantly by the presence of
iron and nickel roadside nano-particles, lining up nicely with the
observations of Mustafa above [22].
The notion
of imprinting information in biology from water molecular structure is by no
means new. Acupuncture practitioners and
homeopathy practitioners have long since
been aware. However, in this
case, our friend Joe would get told we are really well into the realms of
quackery, but are we? First we need to
consult the experimental work of highly respected Emeritus professor
Cyril Smith. Smith’s work developed over the past 40 years
starting from dielectric measurements on enzymes and the subsequent finding
that the measurements were affected by electric, magnetic, electromagnetic
fields and quantum fields. A request for help in the diagnosis and therapy of
chemically sensitive patients who had
also become sensitive to their electromagnetic environment came to Smith
in 1982 [24]. He found that the same physical or mental symptoms in those afflicted could be provoked by a
chemical or a frequency challenge and this led to an appreciation
of the synergy between chemical and frequency environmental sensitivities.
Experimental cooperation with theoretical physicist Herbert Fröhlich FRS and
others led to an understanding of the physics of coherent water in living
systems and a mechanism for the memory of water for coherent frequencies. In a coherent system there are interacting
frequencies proportionate to any velocity the system will support, in
particular the velocity of light and the velocity of coherence diffusion. Thus, there can be biological interaction
between the optical, microwave and ELF spectral regions. Smith even discussed frequency modulation of
light scattered by bio-fields and its retention in recorded images. A 'nil-potent' frequency can erase a
frequency signature and thence affect a biological system. Homeopathy is
interpreted through the biological effects of coherent frequencies derived from
the frequency signature of the 'Mother Tincture' and developed through dilution
and succussion. A homeopathic potency has a frequency signature therefore it
must be able to have a biological effect. Secondly. we need to consider the work of brilliant sh
theoretical Physicists such as Persinger and
Pitkanen and finally we need to look at the experimental evidence that
the refractive index of water has been shown to be modulated by the Erath’s
pico Tesla magnetic field, see D’ Emilia et al (2016).
In the near field of a transmitter (antenna) the
phase relationships which satisfy information imprinting are not necessarily
present and this could explain geometry critical effects in previous
experiments to try and establish a link between RF and genetic damage. Lauer (ref) has discussed RF and cancer in terms of
populations of T-cells. With high
levels of e-field and in the near field, I have previously suggested the required phase relationship for bio-
imprinting is not likely to be satisfied. Secondly, people exposed in this way,
usually military radio operators and radio amateurs use multiple frequencies
and modulation schemes so will build up good distributions of T-cells following
Lauer ( ). Thirdly, their exposure times are often very short as they often
spend more time listening (receiving) than transmitting. Thus the overall
effect of their high frequency
operations may be mainly cancer neural or even anti-cancer. This would
then also explain why their predominant cancers are leukaemia which is perhaps
more a feature of exposure to 50/60 Hz magnetic fields in the power transformers of their equipment.
Added
tiers of complexity: Frequency windowing
The Rife machine, claimed to be anticancer uses and
RF carrier wave in the near field of the patient with a number of very specific
( frequency window or resonance style)
amplitude modulated sideband frequencies in the kHz range. We have
also seen above that Barbault et al (2009) , Costa et al ( 2011) and Zimmermann et al (2011) also describe
frequency windowing or resonance like effects.
Their system uses a 27 MHz carrier and different modulation frequencies
ranging from low hundreds of Hertz to about 21 KHz. Moreover, they report different frequencies
for different types of cancer. It has
been suggested by some that the high carrier frequency may be a vehicle for
getting the frequencies inside the cell.
This is perfectly feasible as membrane relaxation frequencies are often
reported as of the order of 1-10 MHz.
The antenna system used is very different from the Rife machine and is
essentially a mouth worn capacitive coupling electrode. Thus despite only about 100mW power level
possibly more RF current will flow through the body. Barbault et al examined a total of 163 patients with a
diagnosis of cancer and identified a total of 1524 frequencies ranging from 0.1
Hz to 114 kHz. Most frequencies (57–92%) were specific for a single tumor type.
Compassionate treatment with tumor-specific frequencies was offered to 28 patients.
Three patients experienced grade 1 fatigue during or immediately after
treatment. There were no NCI grade 2, 3 or 4 toxicities. Thirteen patients were
evaluable for response. One patient with hormone-refractory breast cancer
metastatic to the adrenal gland and bones had a complete response lasting 11
months. One patient with hormone-refractory breast cancer metastatic to liver
and bones had a partial response lasting 13.5 months. Four patients had stable
disease lasting for +34.1 months (thyroid cancer metastatic to lung), 5.1
months (non-small cell lung cancer), 4.1 months (pancreatic cancer metastatic
to liver) and 4.0 months (leiomyosarcoma metastatic to liver). Their conclusion
was cancer-related frequencies appear to
be tumor-specific and treatment with tumor-specific frequencies is feasible,
well tolerated and may have biological efficacy in patients with advanced
cancer.
In an in vitro attempt to duplicate the in vivo
experiment Zimmermann et al showed the
growth of HCC and breast cancer cells was significantly decreased by
HCC-specific and breast cancer-specific modulation frequencies, respectively.
However, the same frequencies did not affect proliferation of non-malignant
hepatocytes or breast epithelial cells. Inhibition of HCC cell proliferation
was associated with downregulation of XCL2 and PLP2. Furthermore, HCC-specific modulation frequencies disrupted the
mitotic spindle.
Zimmermann et al (2013) described a rationale for
the Therapeutic Use of Amplitude-modulated Radiofrequency Electromagnetic
Fields for the Systemic Treatment of Cancer.
I feel the next part of their argument rather elegantly shows the
advantage of and rationale for using a high frequency carrier wave. For example, they state they have
previously identified several frequencies in patients with chronic insomnia
using biofeedback methods. They demonstrated that the intra-buccal
administration of very low and safe levels of 27.12 MHz RF EMF,
amplitude-modulated at 42.7 Hz, has a sleep-inducing effect in healthy
subjects. However, administration of the same signal to patients with insomnia
did not yield any therapeutic benefits. In contrast, administration of a
combination of the four frequencies most commonly identified in patients with
chronic insomnia (2.7 Hz, 21.9 Hz, 42.7 Hz, and 48.9 Hz) resulted in
significant improvements of total sleep time and sleep latency as assessed by
polysomnographic evaluation[ Thus their
early findings suggested that a combination of several frequencies is
needed to achieve a therapeutic effect on chronic insomnia and a rationale for
continuation once they had established by biofeedback methodologies specific frequencies for some types of
cancer.
Theories
of resonance and links to the mitotic
spindle
It has long been established that dividing yeast
cells emit bio fields. Further it is
established there is a biological electric field gradient across wounded, cut
or damaged tissue. The fact that bio-electromagnetic fields
exist suggests that they ought to be able to be coupled to or influenced
by external influence.
There exist only two plausible mechanisms for such
coupling if it is also to effect the mitotic spindle. Following
Frolich, Zhoa et al (2012) has
suggested that long since proposed Super-macromolecular complexes play many
important roles in eukaryotic cells. Classical structural biological studies
focus on their complicated molecular structures, physical interactions and
biochemical modifications. Recent advances concerning intracellular electric
fields generated by cell organelles and super-macromolecular complexes shed new
light on the mechanisms that govern the dynamics of mitosis and meiosis. In
this review we synthesize this knowledge to provide an integrated theoretical
model of these cellular events. They further
suggest that the electric fields generated by synchronized oscillation
of microtubules, centrosomes, and chromatin fibers facilitate several events
during mitosis and meiosis, including centrosome trafficking, chromosome
congression in mitosis and synapsis between homologous chromosomes in meiosis.
These intracellular electric fields are generated under energy excitation
through the synchronized electric oscillations of the dipolar structures of
microtubules, centrosomes and chromosomes, three of the super-macromolecular
complexes within an animal cell.
Funk et al
deal with low frequency electromagnetic field effects on ultra-weak
photon emission from yeast cells Saccharomyces cerevisiae. The current state of
the research of electromagnetic field interactions with biological systems is
shortly presented and the phenomenon of ultra-weak photon emission from
biological samples is briefly introduced. Critically and as I proposed, Their experimental results indicate the differences
in dynamics of ultra-weak photon emission between cells exposed to magnetic
field and controls cells. Results suggest potential applicability of
this method for the evaluation of magnetic field effects on cells.
Caligiuri has
also suggested a possible mechanism of interaction along my lines of
thought involving the resonant
absorption of electromagnetic radiation by microtubules. To this aim they have
been modelled as non-dissipative forced harmonic oscillators characterized by
two coupled “macroscopic” degrees of freedom, respectively describing
longitudinal and transversal vibrations induced by the electromagnetic field.
They have shown that the proposed model,
although at a preliminary stage, is able to explain the ability of even weak
electromagnetic radiating electromagnetic fields to transfer high quantities of
energy to living systems by means of a resonant mechanism, so capable to easily
damage microtubules structure.
Frolich was essentially dealing with
Bio-solitons. A Bio-Soliton Model that
predicts Non-Thermal Electromagnetic Radiation Frequency Bands, that either
Stabilize or Destabilize Life Conditions has been proposed by Geesink
and Meijer (2016).
Solitons,
as self-reinforcing solitary waves, interact with complex biological phenomena
such as cellular self-organisation. Soliton models are able to describe a
spectrum of electromagnetism modalities that can be applied to understand the
physical principles of biological effects in living cells, as caused by
electromagnetic radiation. A bio-soliton model is proposed, that enables to
predict which eigen-frequencies of non-thermal electromagnetic waves are
life-sustaining and which are, in contrast, detrimental for living cells. The
particular effects are exerted by a range of electromagnetic wave frequencies
of one-tenth of a Hertz till Peta Hertz, that show a pattern of twelve bands,
if positioned on an acoustic frequency scale. The model was substantiated by a
meta-analysis of 240 published papers of biological radiation experiments, in
which a spectrum of non-thermal electromagnetic waves were exposed to living
cells and intact organisms. These data support the concept of coherent
quantized electromagnetic states in living organisms and the theories of
Davydov, Frohlich and Pang. A spin-off strategy from their study is discussed in order to design
bio-compatibility promoting semi-conducting materials and to counteract
potential detrimental effects due to specific types of electromagnetic
radiation produced by man-made electromagnetic technologies.
Ion
cyclotron resonance
Ion cyclotron resonance as a means of interaction
between non –ionising radiation and biology was proposed as far back as 1991.
When a physical mechanism is suggested for a resonant interaction of weak
magnetic fields with biological systems. An ion inside a Ca2+ -binding protein
is approximated by a charged oscillator. A shift in the probability of ion
transition between different vibrational energy levels occurs when a
combination of static and alternating magnetic fields is applied. This in turn
affects the interaction of the ion with the surrounding ligands. The effect
reaches its maximum when the frequency of the alternating field is equal to the
cyclotron frequency of this ion or to some of its harmonics or sub-harmonics. A
resonant response of the biosystem to the magnetic field results.
The fact that
a 147 MHz carrier wave pulse modulated at 16 Hz has been shown to elicit
Calcium ion efflux from chick brain tissue is most likely a facet of ion
cyclotron resonance. The work was
originally criticised due to concerns about oxygen perfusion and tissue
treatment but the work has recently been successfully reproduced in an
independent laboratory. Moreover the
findings of others provide strong
evidence that transport of a given ionic species through a cell membrane can be
precisely controlled by tuning externally applied magnetic fields to the ion
cyclotron resonance (CR) gyrofrequency for the ion in question. Experiment and
theory have shown that certain odd harmonics of the fundamental resonance
frequency are also effective. In the present experiment we again used the model
of Ca-dependent motility of benthic diatoms, extending our harmonic studies
through N = 17, for both Ca2+ and K+ fundamentals. Eight separate Ca2+ fundamental
frequencies: 8, 12, 16, 23, 31, 32, 46, 64 Hz were attempted and each was found
to obey the CR condition. Two observations are reported : (1) tuning to K+
results in inhibition of motility, directly opposite to the enhancement that
occurs when tuning for Ca2+; (2) both the K+ inhibition and Ca2+ enhancement
are independently observed at exactly the same harmonics: N = 1, 3, 5, 15. This
strongly suggests that despite differences in ionic selectivity, K+ and Ca2+
channels may share fundamentally similar protein configurations.
Molecular biology could link the action of ion
transporters and ion channels to the “electric” action of cells and tissues.
The triggers exerted by ion concentrations and concomitant electric field
gradients have been traced along signalling cascades till gene expression
changes in the nucleus. Moreover
cyclotron resonance condition on such ions readily leads to a predicted
ELF-coupling at geomagnetic levels.
The movement of biological ions is of course predicted by cyclotron resonance. Such theory applied to cell membranes has
been tested in employing Diatoms (Amphora coffeaeformis), which were chosen as the bio system since they move
or don't move, depending on how much calcium is transported across the
membrane. The experiments demonstrate that a particular ion (calcium) is
apparently moved across the cell membrane in response to the DC and AC values
of magnetic flux densities (B) and the frequency derived from the cyclotron
resonance theory. A clear resonance is shown and a rather sharp frequency
response curve is demonstrated. The experiments also show a dose response as
the AC value of the flux density is varied, and that odd harmonics of the basic
cyclotron frequency are also effective.
The cyclotron resonance concept is also consistent with recent indications
showing that many membrane channels have helical configurations. This model is
quite testable, and could probably be
applied to other circulating charge components within the cell and, most
important, leads to the feasibility of direct resonant electromagnetic energy
transfer to selected compartments of the cell.
In the study, Bioelectromagnetics 24:395–402, 2003.
© 2003 Wiley-Liss, Inc., the influence of extremely low frequency (ELF)
magnetic fields on the transport of Ca2+ was studied in a biological system
consisting of highly purified plasma membrane vesicles. Two quantum mechanical
theoretical models were tested that assume that biologically active ions can be
bound to a channel protein and influence the opening state of the channel.
Vesicles were exposed for 30 min at 32 °C and the calcium efflux was studied
using radioactive 45Ca as a tracer. Static magnetic fields ranging from 27 to
37 μT and time varying magnetic fields with frequencies between 7 and 72
Hz and amplitudes between 13 and 114 μT (peak) were used. It was show experimentally that suitable combinations of
static and time varying magnetic fields directly interact with the Ca2+ channel
protein in the cell membrane, and we could quantitatively confirm the model
proposed by Blanchard.
Links to
the mitotic spindle and damage thereto
Some modern chemotherapy agents are tubulin
polymerization disruptors. The question arises can electromagnetic absorption
by any of the above mechanism be shown to achieve the same, thereby completing
a complete physical picture and mechanism where by subtle field/ subtle
modulation cancer treatment systems
actually work.
Caligiuri has shown that Microtubule assembly is
regulated by Ca2+-loaded calmodulin (Ca2+/CaM) both in the intact cell and
under in vitro conditions via direct interaction with microtubule-associated
proteins. Here we provide the first evidence that Ca2+/CaM interacts also with
Par17 in a physiologically relevant way, thus preventing Par17-promoted
microtubule assembly. In contrast, parvulin 14 (Par14), which lacks only the
first 25 N-terminal residues of the Par17 sequence, does not interact with
Ca2+/CaM, indicating that this interaction is exclusive for Par17. Pulldown
experiments and chemical shift perturbation analysis with 15N-labeled Par17
furthermore confirmed that calmodulin (CaM) interacts in a Ca2+-dependent
manner with the Par17 N terminus. The reverse experiment with 15N-labeled
Ca2+/CaM demonstrated that the N-terminal Par17 segment binds to both CaM lobes
simultaneously, indicating that Ca2+/CaM undergoes a conformational change to
form a binding channel between its two lobes, apparently similar to the
structure of the CaM-smMLCK796–815 complex. In vitro tubulin polymerization
assays furthermore showed that Ca2+/CaM completely suppresses Par17-promoted
microtubule assembly. The results imply that Ca2+/CaM binding to the N-terminal
segment of Par17 causes steric hindrance of the Par17 active site, thus
interfering with the Par17/tubulin interaction. This Ca2+/CaM-mediated control
of Par17-assisted microtubule assembly may provide a mechanism that couples
Ca2+ signalling with microtubule function.
Thus we now have a direct link between RF input, Calcium
ion movement and staging of the
microtubule assembly. Microtubules are
of course an essential component of the mitotic spindle. In mitosis itself the situation is even
more complex as there is involvement of the endoplasmic reticulum and micro-calcium
domains.
Further evidence that the fields required may be
much lower than previously expected has been given by Sardari and Verger
(2010). It is already known that
electrostatic, magnetostatic, extremely low-frequency electric fields, and pulsed
electric field could be utilized in cancer treatment. The healing effect
depends on frequency and amplitude of electric field. In their work, a simple theoretical model is developed
to estimate the intensity of electrostatic field that damages a living cell
during division. By this model, it is shown that magnification of electric
field in the bottleneck* of the dividing
cell is enough to break chemical bounds between molecules by an avalanche
process. Our model shows that the externally applied electric field of
4 V/cm intensity is able to hurt a cancer cell at the dividing
stage.
At the
‘bottleneck’ point of mitosis I would independently expect field
magnification, since we are effectively falling from having whatever potential difference is presented
being initially across micrometre dimensions being effectively reduced down to
nanometre dimensions.
Explaining
the observations of specific frequencies for treating cancer.
We can now begin to see why there should be
exposure time, amplitude and frequency critical domains in different tissue and
tumour types. For example some types of
cancer cells are more acidic than normal cells, see Griffiths 1991 and Stubbs
(2000). Stubbs comments that the acidic
environment may lead to new treatment strategies. Certainly it will lead to different ion gradients and hence
different cyclotron resonance frequencies.
Likewise there will be different
micro-environment for the mitotic spindle, different mechanical properties and
stiffness and hence different
resonance frequencies. Here and thus I propose this elegantly
explains the hitherto totally
unexplained observations of Barbault et al (2009).
Change in cell stiffness is a new characteristic of
cancer cells that affects the way they spread.
Using atomic force microscopy, Cross et al (2007) reported on the stiffness of live metastatic cancer cells
taken from the body (pleural) fluids of patients with suspected lung, breast
and pancreas cancer. Within the same sample, they found that the cell stiffness
of metastatic cancer cells is more than 70% softer, with a standard deviation
over five times narrower, than the benign cells that line the body cavity.
Different cancer types were found to display a common stiffness. Their work suggested
that mechanical analysis would distinguish cancerous cells from normal ones
even when they show similar shapes. Their
results showed that nano-mechanical analysis correlates well with
immuno-histochemical testing currently used for detecting cancer.
And, in the present authors’ opinion fully explain
why different sets of specific subtle
frequencies are needed to treat
cancer at non-thermal energies.
Conclusions
and Explaining the significant differences between RF involvement in cancer causation
and cure.
I)
Cancer causation
I have
dealt extensively with the topic before but other than the effect of reduced
melatonin, not discussed above, free radical generation is the most general
effect of RF radiation. Free radicals increase lipid peroxidation and Diplock
et al (1994) have shown peroxidation is increased in the malignant state.
II)
Cancer treatment ( non –thermal non-ionising radiation)
Resonance effects disrupting the mitotic spindle
either direct mechanical disturbance
and/or via effects of cyclotron resonance on calcium ions.
Polymerisation of tubulin is prevented so the cell cycle is halted and
proliferation can no longer occur.
Because tumour cell microenvironments especially acidity are changed so
are their cellular stiffness which is
also different by cell line type and
significantly lower than that of healthy cells , a different set of treatment
frequencies is to be expected for each cancer type and healthy cells will be
unaffected. This is exactly as is observed by Barbault et al (2009).
Now that I have provided a proper physical basis
for Barbault’s work I would hope these types of technology will be thoroughly
and quickly developed to the benefit of all human kind. There is also no reason
to suppose spin –offs for treating animal cancers will not be possible
also.
The final
link in the Chain: Geisner’s Clathrate RNA replicator
We have established a number of valid mechanisms
for subtle field cancer treatment but other than those frequencies reported by
Barbault et al (refs) many of which appear to be undisclosed even in their
patent, we have now way of predicting
exactly what frequencies should do what.
In order to look for a solution we need to consider
the very origins of life itself. The
"creation of man from clay" is a theme that recurs throughout world
religions and mythologies. Examples include:
According
to Sumerian mythology the god Enki or Enlil create a servant of the gods,
humankind, out of clay and blood. See Enki and the Making of Man
In
another Sumerian story, both Enki and Ninmah create humans from the clay bowl
of the Abzu, modern day Africa, in which the ovum of a humanoid is fertilized
with the sperm of the Anunnaki and inserted back into an Anunnaki heroine.
According
to Genesis 2:7 "And the Lord God formed man of the dust of the ground, and
breathed into his nostrils the breath of life; and man became a living
soul."
According
to the Qur'an, God created man from clay.
According
to Greek mythology, Prometheus created man from clay, while Athena breathed
life into them.
According
to Chinese mythology (see Chu Ci and Imperial Readings of the Taiping Era),
Nüwa moulded figures from the yellow earth, giving them life and the ability to
bear children.
According
to Egyptian mythology the god Khnum creates human children from clay before
placing them into their mother's womb.
According
to some American Indian beliefs, the Earth-maker formed the figure of many men
and women, which dried in the sun and
into which he breathed life.
According
to Inca mythology the creator god Viracocha formed humans from clay on his
second attempt at creating living creatures.
According
to some Laotian mythology, there are stories of humans created from mud or
clay.
Intriguingly modern science reaches the same
conclusion. The notion that life began
on clay crystals is, in science, only some 50 years old, not several thousand however,
For more than
50 years science has proposed the Clathrate structure as one which could
catalyse primitive RNA replication., http://exploringorigins.org/nucleicacids.html. Indeed, Cains-Smith (1982) has suggested that
clay minerals can store and replicate structural defects, dislocations, and
ionic substitutions, and act as ‘genetic candidates’.
Enter Geesink
who has combined our clathrate origins with the bio-soliton and quantum
mechanics. Geisner then elegantly
shows how that crystalline dimensions of montmorillonite , one particular
clathrate structure would be absolutely the most ideal to replicate RNA, in primordial pre DNA
world.
Further Geesink
provides the equivalent THz frequencies for such a clathrate
resonator. He then scales these and
reduces them to a condensate
scale from 256-488 Hz by dividing by powers of two. If one considers the enormous number of
molecular sub-units available for folding and the like in biology it seems
perfectly feasible that low frequency condensates can also exist as real entities. This then becomes analogous with Frolich’s
coherence theory and also goes some way to explaining frequency analysis of
acupuncture points ( refs).
Further Geesink
has considered some experiments which have been done on monitoring RF
radiation emissions from and bio –effect on living systems, especially
yeasts. The conclusion is that to
within a tiny percentage error radio or vibrational emissions are received
at/on the life –stabilising condensates
and when transmissions are made on these frequencies there is either no
bio-effect or safe or useful bio-effect.
However, when transmissions are made into a biological system at frequencies
in-between the condensates (life destabilisation frequencies according to Geesink and further accordingly where adverse
biological effects are likely to occur), hereinafter ‘anti-condensates’
according to the present author. It
has been somewhat difficult to validate all of Geesink’s work because many
of the long list of references he quotes
in connection with his ‘life stabilising frequencies’ have for whatever reason proved
inaccessible even via Google Scholar.
Crucially, however, most of the frequencies Geesink views as destructive or life
destabilising are associated with experiments which have shown effects of RF radiation
deleterious to bio-systems. It must
be borne in mind, however, that the totality of some 5,000 different works
covering all aspects of RF radiation,
occupational epidemiology, geo-spatial epidemiology, in vivo animal
experimentation, in vivo cell culture and organ experimentation has neither
been considered by Geiesink nor myself,
although a significantly representative cross-section has been so
considered. So much so that I can
cite the work of numerous authors using at first sight completely different frequencies/ and/or modulation
schemes achieving the same result when their particular experimental frequency
has been reduced by myself to its condensate equivalent.
According to the present author, Geesink’s definition of ‘life stabilising’
and life ‘de-stabilising’ is very much
an over-simplification because with regards to
life, Geesink was referring to
the development of all life, not just
human or mammalian life. Thus, for example, some of the Geesink’s life
stabilising frequencies actually
encourage the growth of certain microbes, not necessarily advantageous to
mammalian /human life, depending of course on the microbe in question.
Re-iterating,
we have seen other groups such as Barbault et al have, recently
but prior to Geesink’s paper, also discovered what they have termed to be
cancer treating modulation frequencies,
but they have proposed no physical mechanism for how this could work and
they are not the frequencies disclosed by the present inventor/invention nor do
they have the same stated mechanisms.
I have very recently analysed a significantly
greater number of reported bio-effects of electromagnetic radiation and ultrasound
( not considered by Geesink) and accordingly have reached additional
important conclusions regarding the condensates
and anti-condensates, hereinafter the key frequencies. For instance I have shown that
these key frequencies have, just as
biology’s specialist organs and
differentiated tissue types, very
specific purposes. Some are growth promoting, certain are
anti-bacterial, certain are always associated with the blood brain barrier and
memory, certain cause calcium efflux,
certain reduce mitochondrial activity, certain cause growth retardation,
certain affect mitosis, certain modulate the cell cycle etc. etc. Because of this I have already filed patent
applications in certain regards. There are quite close parallels here,
I feel, with Smith’s work on frequency effects in acupuncture and
homeopathy(refs).
Furthermore I
have also very recently indeed
considered the influence of the primordial electromagnetic environment Geisner’s condensate frequencies.
The view I take is at the dawn of evolution, earth would have only received signals at
Schumann resonance ( Hz), narrowband
KHz and MHz signals from Jupiter and
broad band microwaves from the Sun and
Galactic Cosmos with specific frequencies in the latter band being attenuated by OH
radicals, hydrogen and water vapour
etc. Thus analysis of these
primordial electromagnetic emissions
leads me to a group of natural frequencies corresponding with Geesink’s
condensate and with my
anti-condensate frequencies which are
solely capable of controlling the finer
bio-physical and biochemical aspects of life itself. What is further incredible is that there are
often multiple examples of Euclid’s element harmonics of each particular
specific key frequency spanning Hz-GHz
capable of bring about the same or very similar bio-effect. This is clearly a vindication of both
Frolich and more latterly Geesink’s work and of the experimental work of
scientists like Pohl (ref) without whom my
further and crucial developmental work would most likely have not been possible. I would just like to add what a great
privilege it was to meet Frolich in his later years personally in the early
1980’s at a conference in Nottingham University.
The
identified frequencies and for life controlling purposes which I have
identified from primordial times are:
PRE-RADIO
(PRIMORDIAL) ELECTROMAGNETIC SPECTRUM
AND PROPOSED INTERACTION WITH CLATHRATE
'BORN' LIFE. |
|
|||||||||||||||||||||||||||||||||||||||
Key Condensate Frequencies |
Schumann Resonance |
|
||||||||||||||||||||||||||||||||||||||
(Clathrate RNA
REPLICATOR) |
plus |
Jupiter |
plus pulsars galactic bursts |
|
||||||||||||||||||||||||||||||||||||
Atmospheric
microwave attenuation (life protecting) |
|
|||||||||||||||||||||||||||||||||||||||
249.5 |
7.8Hz |
15.5Hz |
31.2Hz allows calcium efflux (1st biomolecular motion /heartbeat etc.) |
|
|
|||||||||||||||||||||||||||||||||||
256 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
262.9 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
269.8 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
278.9 |
37 GHz ATP regulation |
|
|
|||||||||||||||||||||||||||||||||||||
288 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
295.6 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
303.1 |
20 MHz |
PLANT GROWTH |
|
|||||||||||||||||||||||||||||||||||||
313.6 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
324 |
11+22 GHz
|
|
|
|||||||||||||||||||||||||||||||||||||
332.6 |
360 +770 GHz Protects
reproduction |
|
|
|||||||||||||||||||||||||||||||||||||
341.2 |
42.7Hz |
Sleep/brain waves |
|
|
||||||||||||||||||||||||||||||||||||
353 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
364.7 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
374.4 |
23.4Hz |
Cell Cycle |
|
|||||||||||||||||||||||||||||||||||||
384 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
394.3 |
420 GHz |
Protects
reproduction |
|
|||||||||||||||||||||||||||||||||||||
404.5 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
418.3 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
432 |
27.3Hz |
60 GHz |
Controls Slows cellular activity fine
balance Schumann versus
atmospheric microwaves |
|
||||||||||||||||||||||||||||||||||||
443.6 |
56.2 kHz |
Control mitosis |
|
|||||||||||||||||||||||||||||||||||||
455.1 |
14.3Hz |
Cell division and
growth |
|
|||||||||||||||||||||||||||||||||||||
470.6 |
WBBBR |
|
||||||||||||||||||||||||||||||||||||||
486 |
8 MHZ |
Cell Division |
|
|||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||
WBBBR= |
Weak |
broad |
band |
background
radiation |
|
|||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||
Table 1
In the key
group of condensate and
anti-condensate frequencies shown above
the frequency 249.5 Hz has a great significance because it is attuned to
several of the Schumann resonance modes. The frequency 278.9 Hz has significance
because it was protected by microwave absorption in the earth’s atmosphere, as
were the frequencies 324, 332.6, 341.2
,394.3 and 432 Hz. The frequencies 374.4 and 455.1 Hz were re-enforced
by Schuman resonance. Further the
frequencies 303.1, 443.6 and 486 Hz were supplied not only by the primitive
clathrate resonator but also by Jovian inputs.
Enter modern wireless
technology.
Modern
wireless technology provides frequencies whose Euclid’s’ elements harmonics or
sub –harmonics which are capable of
falling on virtually all the above key frequencies and thus, potentially
over-riding the natural frequency inputs and
interfering with biological processes leading perhaps in some cases to the initiation or promotion cancer.
A fuller analysis of the present day electromagnetic spectrum in
relation to the aforesaid key frequencies according to the present inventor and
invention is shown in Table 2
below:
COMBINED MODERN AND PRIMORDIAL EM
SPECTRUM
Condensate Key Frequencies Schumann Resonance
E/M SOURCE (Clathrate RNA REPLICATOR) plus Jupiter
plus pulsars galactic bursts
Atmospheric
microwave attenuation (life protecting)
3G 2.1 GHZ/DME/TACAN 249.5 7.8 15.5 31.2 allows calcium efflux (1st
biomolecluar motion/heartbeat etc)
GSM PULSE/TETRA
PULSE/3G 256 oncogene
induction
GERMAN RAILWAYS/VHF
PAGERS 262.9 effect unknown
DME/TACAN 269.8 cell
division effects
WARC 18.1 MHZ/VHF
PAGERS/UHF TV /3G/WIFI 278.9 37 GHz ATP regulation
VHF PAGERS/WIFI 288 cell
division effects
WIFI/3G 295.6 targets
mitotic spindle
MEDICAL U/S/UHF
TV/WIFI 303.1 20 MHz PLANT
GROWTH
WARC BAND 10.1 MHZ, UHF
TV 313.6 membrane
permeability/immune system effects
H.F. HAM RADIO/UHF TV
/GPS 324 11+22
GHz Brain activity
WIND TURBINE
BCF/GSM/VHF FM RADIO 332.6 360 +770
GHz Protects reproduction
UHF TV/VHF FM 341.2 42.7 Sleep/brain waves
2G,3G 1800MHZ/GSM 353 Brain
effects/growth retardation
MEDICAL U/S/VHF FM
RADIO/UHF TV 364.7 Changes
fibroblast growth rates
TETRA/VHF FM/UHF
TV/DME/TACAN 374.4 23.4 Cell Cycle
WARC 24.89 MHZ 384 Kills
bacteria
2G 835/900 MHZ/GPS 394.3 420
GHz Protects reproduction
GPS/DAB 404.5 kills
bacteria
PMR RADIO/DAB 418.3 kills
algae /tetragenic
RADIO WALES
MW/2G/3G/DAB/UHF PMR 450 432 27.3 60 GHz Controls
Slows cellular activity fine balance Schumann versus atmospheric microwave.
2G/3G 1800/GPS/UHF TV 443.6 56.2
kHz Control mitosis
MEDICAL U/S/GPS 455.1 14.3 Cell division and
growth
MEDICAL U/S/OLD VHF
TV/3G 470.6 Controls mitosis
VHF PAGERS 137
MHZ/DME/TACAN 486 8 MHZ Cell
Division
Table 2
My further
private research has allowed the specific bio-effects of individual frequencies
within the group to be quantified and evaluated.
Using a
portable spectrum analyser, I have found, perhaps as expected, that the radio frequency environment varies
tremendously from one location to another.
I decided to analyse locations with known cancer cases of animal and
human cancer. I have noted time after
time Locations where people are living with the most aggressive forms of cancer have been
shown to have at least multiple frequencies which reduce by Euclid’s elements
to 256 Hz, the oncogene induction frequency and at 374.4Hz the cell cycle
frequency. This is not necessarily
trying to say that RF exposure causes all cancers as I have published before RF
radiation acts more as a promoter than an initiator. A typical example of the frequency analysis
at a location where both human and animal cancer was found is shown in Table 3
below:
Atmospheric
microwave attenuation ( life protecting) |
||||||||||||
No. of sources |
249.5 |
7.8Hz |
15.5Hz |
31.2Hz |
allows calcium
efflux (1st biomolecular motion/heartbeat etc.) |
|||||||
2 |
256 |
WBBBR |
|
|
|
ONCOGENE INDUCTION |
3G + GPS |
|
||||
262.9 |
WBBBR |
|||||||||||
269.8 |
WBBBR |
|||||||||||
2! |
278.9 |
|
|
|
37 GHz |
ATP regulation |
|
2 WIFI |
|
|||
1 |
288 |
WBBBR |
|
|
|
CELL MULTIPLICATION |
TETRA |
|
||||
295.6 |
WBBBR |
|||||||||||
303.1 |
20 MHz |
PLANT GROWTH |
||||||||||
313.6 |
WBBBR |
|||||||||||
324 |
11+22 GHz |
Brain activity |
||||||||||
332.6 |
360 +770 GHz |
Protects
reproduction |
||||||||||
341.2 |
42.7Hz |
Sleep/brain waves |
||||||||||
353 |
WBBBR |
|||||||||||
364.7 |
WBBBR |
|||||||||||
5! |
374.4 |
|
23.4Hz |
|
|
|
Cell Cycle |
|
2 VHF FM/TETRA/UHF
TV/GPS |
|||
1 |
384 |
WBBBR |
||||||||||
394.3 |
420 GHz |
Protects
reproduction |
||||||||||
1 |
404.5 |
WBBBR |
||||||||||
418.3 |
WBBBR |
2G |
||||||||||
432 |
27.3Hz |
60 GHz |
Controls Slows
cellular activity fine balance Schumann versus atmospheric microwave. |
|||||||||
1 |
443.6 |
|
|
56.2 kHz |
|
Control mitosis |
|
2G |
||||
455.1 |
14.3Hz |
Cell division and
growth |
||||||||||
470.6 |
WBBBR |
|||||||||||
486 |
8 MHZ |
Cell Division |
||||||||||
WBBBR= |
Weak |
broad |
band |
background
radiation |
Table 3.
Note, in
table 3 above two anthropogenic frequencies are seen to impinge on
the condensate known to cause oncogene induction and five on the
condensate controlling cell cycle. It is presently confirmed that x and
gamma ray radiation, chemical carcinogens and viral infections can lead to
activation of oncogenes. Several activation modes are:
Point mutation
Gain exogenous promoters
Reduction of methylation level
Increased oncogene copy number
Gene translocation or rearrangement
However, the
frequency mode is newly disclosed and thus aspects of which have been protected
in my patent applications.
Accordingly,
then I have shown that a very specific
group of frequencies can kill bacteria and influence cellular processes to
bring about the state we know as cancer.
It logically follows that by similar mechanisms, it is possible to intervene in disease
progression of such as infections and molecular diseases such as for example
cancer by appropriate choice of frequency.
Again I have already filed to protect these important aspects by
patents.
Cancer drugs
which are alkylating agents include chlorambucil, cyclophosphamide, thiotepa,
and busulfan. are cell cycle phase nonspecific, meaning that they kill the cell
in various and multiple phases of the cell cycle. Antimetabolites including
purine antagonists, pyrimidine antagonists, and folate antagonists target
specific parts of the cell cycle. Plant
alkaloids are antitumor agents derived from plants. These drugs act
specifically by blocking the ability of a cancer cell to divide and become two
cells. Although they act throughout the cell cycle, some are more effective
during the S- and M- phases, making these drugs cell cycle specific. Examples
of plant alkaloids used in chemotherapy are actinomycin D, doxorubicin, and
mitomycin. Antitumor antibiotics are
cell cycle nonspecific. They act by binding with DNA and preventing RNA
(ribonucleic acid) synthesis, a key step in the creation of proteins, which are
necessary for cell survival. They are not the same as antibiotics used to treat
bacterial infections. Rather, these drugs cause the strands of genetic material
that make up DNA to uncoil, thereby preventing the cell from reproducing.
Doxorubicin, mitoxantrone, and bleomycin are some examples of antitumor
antibiotics. Large doses of anti-cancer drugs will kill more cells,
greater amounts of drugs will produce more severe side effects.
The group of frequencies above used
appropriately (Confidential and
not fully disclosed here) can target the cell cycle either in a
drug -free manner or augmenting
drug effects and in a relatively side -effect free manner.
Modern cancer
drug treatments target a number of biochemical pathways in addition to cell
cycle. For example calcium channel blockers such as verapamil have recently been shown to
sensitise resistant cancer cells to certain cancer drugs possibly due to a decrease in calmodulin
activity as a result of a drug-induced alteration of the intracellular calcium
environment. Advantageously I have
also discovered a cancer treating frequency which has a similar mode of action.
Adenosine-5’-triphosphate
(ATP) is the main energy source for all forms of work inside our cells. It has
recently been found that even a short-term shortage of ATP supply can be fatal
for cancer cells because activation of a mitochondria-addressed cell death
pathway. specifically targets the
altered energy supply chains of cancer cells, especially brain cancer cells to get theses cells to commit suicide. I have also discovered a group of
frequencies which causes this to happen. These too are presently
Confidential.
Elevated
rates of reactive oxygen species (ROS) have been detected in almost all
cancers, where they promote many aspects of tumor development and progression.
However, tumor cells also express increased levels of antioxidant proteins to
detoxify from ROS, suggesting that a delicate balance of intracellular ROS
levels is required for cancer cell function. Further, the radical generated,
the location of its generation, as well as the local concentration is important
for the cellular functions of ROS in cancer.
I also discovered a frequency which causes the fine tuning of
ROS. This too is presently
confidential.
Cancer cell
undergo uncontrolled abnormal mitosis. These renegade cells escape the normal
controls of mitotic cell division. I
have also discovered a frequency which slows mitosis especially of cancerous
liver cells.
Comprehensive patents have been filed on
both frequency groups and apparatus for treatment.
Further work
Further work on the treatment side will
involve securing the right partners to bring about animal and human clinical
trials. Most likely I will form my own
company to create the equipment.
Further work
on the causation side will focus on much larger scale spectral studies of
cancer cluster locations.
Acknowledgments
I wish to
acknowledge my wife Gwyneth and my son Dwain for on and interesting discussions
on the topic and Gwyneth especially for being my driver and lab assistant on
some of the geo-spatial operations.
References
A
comprehensive reference list will be published in due course but in the
meantime and in the interests of human kind I am releasing the paper in Beta
form as soon as possible.
1. http://bbs.hwrf.com.cn/downebd/35701d1231290960-m61101_3057.pdf
2.
http://onlinelibrary.wiley.com/doi/10.1002/qua.560020505/full
3. http://www.biomag.net/testsite/index_htm_files/PEMF_Fx_abstracts.pdf
4. http://jeccr.biomedcentral.com/articles/10.1186/1756-9966-28-51
5. https://www.ncbi.nlm.nih.gov/pubmed/16949995
6. https://www.ncbi.nlm.nih.gov/pubmed/6093530
7. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188936/
8. 8. http://www.nature.com/bjc/journal/v106/n2/full/bjc2011523a.html
9. http://pubmedcentralcanada.ca/articlerender.cgi?artid=1066776
12. http://www.yeastgenome.org/reference/S000140874/overview
13. https://www.ncbi.nlm.nih.gov/pubmed/19028599
14. https://arxiv.org/ftp/q-bio/papers/0606/0606009.pdf
15. Kliukiene et al, Epidemiol. 2004 May 1;159(9):852-61
16. als.lww.com/epidem/Abstract/2001/01000/The_Possible_Role_of_Radiofrequency_Radiation_in.3.aspx
17. 17. http://www.thecelltowers.org/wp-content/uploads/2013/10/Base_Station-risks.pdf
18. 18. http://redwood.psych.cornell.edu/courses/psych527fall05/additional/dan831/webb.pdf
19. http://www.vincent-lauer.fr/cancer-autoimmunity.pdf
20. http://www.drchrisbarnes.co.uk/Unified.htm
22. https://www.researchgate.net/publication/255769813_Iron_oxide_nanoparticle-based_radio-frequency_thermotherapy_for_human_breast_adenocarcinoma_cancer_cells
23. http://drchrisbarnes.co.uk/More%20egg%20than%20chicken.html
24. http://europepmc.org/abstract/med/26678733
25.