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Magnesium and Cancer Research

_http://magnesiumforlife.com/medical-application/magnesium-and-cancer/_

(http://magnesiumforlife.com/medical-application/magnesium-and-cancer/)

 

 

Magnesium repletion produced rapid

disappearance of the periosteal tumors.[1]

 

 

Aleksandrowicz et al in Poland conclude that inadequacy of magnesium and

antioxidants are important risk factors in predisposing to leukemias.[2]

Other researchers found that 46% of the patients admitted to an ICU in a

tertiary cancer center presented hypomagnesemia. They concluded that the

incidence of hypomagnesemia in critically ill cancer patients is high.[3] In

animal studies we find that magnesium deficiency has caused lymphopoietic

neoplasms in young rats. A study of rats surviving magnesium deficiency

sufficient to cause death in convulsions during early infancy in some, and

cardiorenal lesions weeks later in others, disclosed that some of survivors had

thymic nodules or lymphosarcoma.[4]

 

 

One would not normally think that Magnesium (Mg) deficiency can

paradoxically increase the risk of, or protect against cancer yet we will find

that

just as severe dehydration or asphyxiation can cause death; magnesium

deficiency can directly lead to cancer. When you consider that over 300 enzymes

and ion transport require magnesium and that its role in fatty acid and

phospholipids acid metabolism affects permeability and stability of membranes,

we can see that magnesium deficiency would lead to physiological decline in

cells setting the stage for cancer. Anything that weakens cell physiology

will lead to the infections that surround and penetrate tumor tissues.

These infections are proving to be an integral part of cancer. Magnesium

deficiency poses a direct threat to the health of our cells. Without sufficient

amounts our cells calcify and rot. Breeding grounds for yeast and fungi

colonies they become, invaders all too ready to strangle our life force and

kill us.

 

 

Over 300 different enzymes systems rely upon magnesium to facilitate

their catalytic action, including ATP metabolism, creatine-kinase

activation, adenylate-cyclase, and sodium-potassium-ATPase.[5]

 

 

It is known that carcinogenesis induces magnesium distribution

disturbances, which cause magnesium mobilization through blood cells and

magnesium

depletion in non-neoplastic tissues. Magnesium deficiency seems to be

carcinogenic, and in case of solid tumors, a high level of supplemented

magnesium

inhibits carcinogenesis.[6] Both carcinogenesis and magnesium deficiency

increase the plasma membrane permeability and fluidity. Scientists have in

fact found out that there is much less Mg++ binding to membrane phospholipids

of cancer cells, than to normal cell membranes.[7]

 

 

Magnesium protects cells from aluminum,

mercury, lead, cadmium, beryllium and nickel.

 

 

Magnesium in general is essential for the survival of our cells but takes

on further importance in the age of toxicity where our bodies are being

bombarded on a daily basis with heavy metals. Glutathione requires magnesium

for its synthesis.[8] Glutathione synthetase requires ?-glutamyl cysteine,

glycine, ATP, and magnesium ions to form glutathione.[9] In magnesium

deficiency, the enzyme y-glutamyl transpeptidase is lowered.[10] According to

Dr.

Russell Blaylock, low magnesium is associated with dramatic increases in

free radical generation as well as glutathione depletion and this is vital

since glutathione is one of the few antioxidant molecules known to

neutralize mercury.[11] Without the cleaning and chelating work of glutathione

(magnesium) cells begin to decay as cellular filth and heavy metals

accumulates;

excellent environments to attract deadly infection/cancer.

 

 

There is drastic change in ionic flux from the outer

and inner cell membranes both in the impaired

membranes of cancer, and in Mg deficiency.

 

 

Anghileri et al[12],[13] proposed that modifications of cell membranes are

principal triggering factors in cell transformation leading to cancer.

Using cells from induced cancers, they found that there is much less magnesium

binding to membrane phospholipids of cancer cells, than to normal cell

membranes.[14] It has been suggested that Mg deficiency may trigger

carcinogenesis by increasing membrane permeability.[15] Magnesium deficient

cells

membranes seem to have a smoother surface than normal, and decreased membrane

viscosity, analogous to changes in human leukemia cells.[16],[17] There is

drastic change in ionic flux from the outer and inner cell membranes (higher

Ca and Na; lower Mg and K levels), both in the impaired membranes of

cancer, and of Mg deficiency. And we find that lead (Pb) salts, are more

leukemogenic when given to Mg deficient rats, than when they are given to

Mg-adequate rats, suggesting that Mg is protective.[18]

 

 

Magnesium has an effect on a variety of cell membranes

through a process involving calcium channels and ion transport

mechanisms. Magnesium is responsible for the maintenance

of the trans-membrane gradients of sodium and potassium.

 

 

Long ago researchers postulated that magnesium supplementation of those

who are Mg deficient, like chronic alcoholics, might decrease emergence of

malignancies[19] and now modern researchers have found that all types of

alcohol — wine, beer or liquor — add equally to the risk of developing

breast

cancer in women. The researchers, led by Dr. Arthur Klatsky of the Kaiser

Permanente Medical Care Program in Oakland, Calif., revealed their findings

at a meeting of the European Cancer Organization in Barcelona in late 2007.

It was found that women who had one or two drinks a day increased their

risk of developing breast cancer by 10 percent. Women who had more than three

drinks a day raised their risk by 30 percent. The more one drinks the more

one drives down magnesium levels.

 

 

Breast cancer is the second most common cancer

killer of women, after lung cancer. It will be diagnosed in

1.2 million people globally this year and will kill 500,000.

 

 

According to data published in the British Journal of Cancer in 2002, 4

percent of all breast cancers — about 44,000 cases a year — in the United

Kingdom are due to alcohol consumption. It’s an important question though,

and one not asked by medical or health officials, is it the alcohol itself or

the resultant drop in magnesium levels that is cancer provoking? Though

some studies have shown that light- to moderate alcohol use can protect

against heart attacks it does us no good to drink if it causes cancer. Perhaps

if magnesium was supplemented in women drinkers who were studied there would

have been no increase of cancer from drinking.

 

 

Alcohol has always been known to deplete magnesium,

and is one of the first supplements given to alcoholics

when they stop and attempt to detoxify and withdraw.

 

 

Researchers from the School of Public Health at the University of

Minnesota have just concluded that diets rich in magnesium reduced the

occurrence

of colon cancer.[20] A previous study from Sweden[21] reported that women

with the highest magnesium intake had a 40 per cent lower risk of developing

the cancer than those with the lowest intake of the mineral.

 

 

Magnesium stabilizes ATP[22], allowing

DNA and RNA transcriptions and repairs.[23]

 

 

The anti-colon cancer effects of calcium are linked to magnesium levels,

says a new study. Researchers from Vanderbilt University found that low

ratios of the minerals were associated with reduced risk of colorectal cancer,

according to findings presented at the Seventh Annual American Association

for Cancer Research International Conference on Frontiers in Cancer

Prevention Research. Both high magnesium and calcium levels have been linked to

reduced risks of colon cancer but studies have also shown that high calcium

levels inhibit the absorption of magnesium. According to Qi Dai, MD, PhD, and

co-workers, Americans have high calcium intake, but also a high incidence

of colorectal cancer. “If calcium levels were involved alone, you’d expect

the opposite direction. There may be something about these two factors

combined – the ratio of one to the other – that might be at play,†said

Dai.

The risk of colorectal cancer adenoma recurrence was reduced by 32 per cent

among those with baseline calcium to magnesium ratio below the median in

comparison to no reduction for those above the median,†said Dai.[24]

 

 

Pre-treatment hypomagnesemia has been reported

in young leukemic children, 78% of whom have histories

of anorexia, and have excessive gut and urinary losses of Mg.[25]

 

 

Several studies have shown an increased cancer rate in regions with low

magnesium levels in soil and drinking water, and the same for selenium. In

Egypt the cancer rate was only about 10% of that in Europe and America. In

the rural fellah it was practically non-existent. The main difference was an

extremely high magnesium intake of 2.5 to 3g in these cancer-free

populations, ten times more than in most western countries.[26]

 

 

The School of Public Health at the Kaohsiung Medical College in,

Taiwan, found that magnesium also exerts a protective effect

against gastric cancer, but only for the group with the highest levels.[27]

 

 

If we looked it would probably be very difficult to find a cancer patient

with anywhere near normal levels of cellular magnesium meaning cancer

probably does not exist in a physical cellular environment full of magnesium.

It

makes perfect medical sense to saturate the body with magnesium through

transdermal means. Magnesium deficiency has been implicated in a host of

clinical disorders but the medical establishment just cannot get it through its

thick skull that it is an important medicine.

 

 

It is as if the collective medical profession had just pulled the plug on

medical intelligence. In fact it has done exactly this and it seems too

late for it to redefine itself, which is a tragedy. Though magnesium improves

the internal production of defensive substances, such as antibodies and

considerably improves the operational activity of white granulozytic blood

cells (shown by Delbert with magnesium chloride), and contributes to many other

functions that insure the integrity of cellular metabolism, no one thinks

to use it in cancer as a primary treatment. It is even worse than this, the

medical establishment does not even use magnesium as a secondary treatment

or even use it at all and gladly uses radiation and chemo therapy, both of

which force magnesium levels down further.

 

 

To not replete cellular magnesium levels would be negligent especially in

the case of cancer where a person’s life is on the line. An oncologist who

ignores his patient’s magnesium levels would be analogous to an emergency

room physician not rushing resuscitation when a person stops breathing. If

one elects to have or has already had chemotherapy they have four times the

reason to pay attention to a concentrated protocol aimed at replenishing

full magnesium cellular stores.

 

 

Magnesium chloride is the first and most important item in any person’s

cancer treatment strategy. Put in the clearest terms possible, our suggestion

from the first day on the Survival Medicine Cancer Protocol is to almost

drown oneself in transdermally applied magnesium chloride. It should be the

first not the last thing we think of when it comes to cancer. It takes

about three to four months to drive up cellular magnesium levels to where they

should be when treated intensely transdermally but within days patients

will commonly experience its life saving medical/healing effects. For many

people whose bodies are starving for magnesium the experience is not too much

different than for a person coming out of a desert desperate for water. It

is that basic to life, that important, that necessary.

 

 

That same power found in magnesium that will save your life in the

emergency room during cardiac arrest, that will diminish damage of a stroke if

administered in a timely fashion is the same power that can save one’s life

if

one has cancer. All a patient has to do is pour it into their baths or

spray it right onto their bodies. What could be simpler?

 

 

Magnesium chloride, when applied directly

to the skin, is transdermally absorbed and has an

almost immediate effect on chronic and acute pain.

 

 

Special Note on Calcium and Cancer:

 

 

Experts say excessive calcium intake may be unwise in light of recent

studies showing that high amounts of the mineral may increase risk of prostate

cancer. “There is reasonable evidence to suggest that calcium may play an

important role in the development of prostate cancer,†says Dr. Carmen

Rodriguez, senior epidemiologist in the epidemiology and surveillance research

department of the American Cancer Society (ACS). Rodriguez says that a 1998

Harvard School of Public Health study of 47,781 men found those consuming

between 1,500 and 1,999 mg of calcium per day had about double the risk of

being diagnosed with metastatic (cancer that has spread to other parts of

the body) prostate cancer as those getting 500 mg per day or less. And those

taking in 2,000 mg or more had over four times the risk of developing

metastatic prostate cancer as those taking in less than 500 mg.

 

 

Calcium and magnesium are opposites in their effects

on our body structure. As a general rule, the more

rigid and inflexible our body structure is, the

less calcium and the more magnesium we need.

 

 

Later in 1998, Harvard researchers published a study of dairy product

intake among 526 men diagnosed with prostate cancer and 536 similar men not

diagnosed with the disease. That study found a 50% increase in prostate cancer

risk and a near doubling of risk of metastatic prostate cancer among men

consuming high amounts of dairy products, likely due, say the researchers,

to the high total amount of calcium in such a diet. The most recent Harvard

study on the topic, published in October 2001, looked at dairy product

intake among 20,885 men and found men consuming the most dairy products had

about 32% higher risk of developing prostate cancer than those consuming the

least.

 

 

The adverse effects of excessive calcium intake may include high blood

calcium levels, kidney stone formation and kidney complications.[28] Elevated

calcium levels are also associated with arthritic/joint and vascular

degeneration, calcification of soft tissue, hypertension and stroke, and

increase

in VLDL triglycerides, gastrointestinal disturbances, mood and depressive

disorders, chronic fatigue, and general mineral imbalances including

magnesium, zinc, iron and phosphorus. High calcium levels interfere with

Vitamin

D and subsequently inhibit the vitamin’s cancer protective effect unless

extra amounts of Vitamin D are supplemented.[29]

 

 

Magnesium is the mineral of rejuvenation and prevents

the calcification of our organs and tissues that is

characteristic of the old-age related degeneration of our body.

 

 

Recommendations of magnesium to calcium ratios range from 1:2 to 1:1. For

those interested in preventing cancer one should look closely at the 1:1

camp and during the first six months of treatment one should be looking at

ten parts magnesium to one part calcium. In reality one need not even count

the ratio during the first months for the only real danger of extremely high

magnesium levels comes with patients suffering from kidney failure. If one

is at all concerned about their calcium intake one should eat foods high

in both calcium and magnesium like toasted sesame seeds.

 

 

Up to 30% of the energy of cells is

used to pump calcium out of the cells.

 

 

Doctors who have used intravenous magnesium treatments know the benefits

of peaking magnesium levels, even if only temporarily. For the cancer

patient the transdermal approach combined with oral use offers the opportunity

to

take magnesium levels up strongly and quickly. For emergency situations

three applications a day, for urgent two treatments would be indicated though

one strong treatment with an ounce of a natural magnesium chloride

solution spread all over the body like a sun screen is a powerful systemic

treatment.

 

 

It is medical wisdom that tells us that magnesium is actually the key to

the body’s proper assimilation and use of calcium, as well as other

important nutrients. If we consume too much calcium, without sufficient

magnesium,

the excess calcium is not utilized correctly and may actually become toxic,

causing painful conditions in the body. Hypocalcemia is a prominent

manifestation of magnesium deficiency in humans (Rude et al., 1976). Even mild

degrees of magnesium depletion significantly decreases the serum calcium

concentration (Fatemi et al., 1991).

 

 

Calcium requirement for men and

women is lower than previously estimated.[30]

 

 

 

 

Mark Sircus Ac., OMD International Medical Veritas Association

_http://imva.info/_ (http://imva.info/)

_http://publications.imva.info_ (http://publications.imva.info/)

_http://www.winningcancer.com/_ (http://www.winningcancer.com/) Email:

_director_ (director)

----------

----

 

[1] Hunt, B.J., Belanger, L.F. Localized, multiform, sub-periosteal

hyperplasia and generalized osteomyelosclerosis in magnesium-deficient rats.

Calcif. Tiss. Res. 1972; 9:17-27.

 

[2]Aleksandrowicz, J., Blicharski, J., Dzigowska, A., Lisiewicz, J. Leuko-

and oncogenesis in the light of studies on metabolism of magnesium and its

turnover in biocenosis. Acta Med. Pol. 1970; 11:289-302. (abstr: Blood

1971; 37:245)

 

[3] D. Deheinzelin, E.M. Negri1, M.R. Tucci, M.Z. Salem1, V.M. da Cruz1,

R.M. Oliveira, I.N. Nishimoto and C. Hoelz. Hypomagnesemia in critically ill

cancer patients: a prospective study of predictive factors. Braz J Med

Biol Res, December 2000, Volume 33(12) 1443-1448

 

[4] Bois, P. Tumour of the thymus in magnesium-deficient rat. Nature 1964;

204:1316.

 

[5] Magnesium is used in the creatine-phosphate formation, activates the

alkaline phosphatase and pyrophosphatase, stabilizes nucleic acid synthesis,

concerning DNA synthesis and degradation, as well as the physical

integrity of the DNA helix, activates amino acid and protein synthesis, and

regulat

es numerous hormones.

 

[6] Durlach J, Bara M, Guiet-Bara A, Collery P. Relationship between

magnesium, cancer and carcinogenic or anticancer metals. Anticancer Res. 1986

Nov-Dec;6(6):1353-61.

 

[7]Anghileri, L.J. Magnesium concentration variations during

carcinogenesis. Magnesium Bull. 1979; 1:46-48.

 

[8] Linus Pauling Institute

_http://lpi.oregonstate.edu/infocenter/minerals/magnesium/index.html#function_

(http://lpi.oregonstate.edu/infocenter/minerals/magnesium/index.html#function)

 

[9] Virginia Minnich, M. B. Smith, M. J. Brauner, and Philip W. Majerus.

Glutathione biosynthesis in human erythrocytes. Department of Internal

Medicine, Washington University School of Medicine, J Clin Invest. 1971 March;

50(3): 507–513. Abstract: The two enzymes required for de novo glutathione

synthesis, glutamyl cysteine synthetase and glutathione synthetase, have

been demonstrated in hemolysates of human erythrocytes. Glutamyl cysteine

synthetase requires glutamic acid, cysteine, adenosine triphosphate (ATP), and

magnesium ions to form ?-glutamyl cysteine. The activity of this enzyme in

hemolysates from 25 normal subjects was 0.43±0.04 ?mole glutamyl cysteine

formed per g hemoglobin per min. Glutathione synthetase requires ?-glutamyl

cysteine, glycine, ATP, and magnesium ions to form glutathione. The activity

of this enzyme in hemolysates from 25 normal subjects was 0.19±0.03 ?mole

glutathione formed per g hemoglobin per min. Glutathione synthetase also

catalyzes an exchange reaction between glycine and glutathione, but this

reaction is not significant under the conditions used for assay of hemolysates.

The capacity for erythrocytes to synthesize glutathione exceeds the rate

of glutathione turnover by 150-fold, indicating that there is considerable

reserve capacity for glutathione synthesis. A patient with erythrocyte

glutathione synthetase deficiency has been described. The inability of

patients’

extracts to synthesize glutathione is corrected by the addition of pure

glutathione synthetase, indicating that there is no inhibitor in the

patients’

erythrocytes.

 

[10] Braverman, E.R. (with Pfeiffer, C.C.)(1987). The healing nutrients

within: Facts, findings and new research on amino acids. New Canaan: Keats

Publishing

 

[11] _http://www.dorway.org/blayautism.txt_

(http://www.dorway.org/blayautism.txt)

 

[12] Anghileri, L.J. Magnesium concentration variations during

carcinogenesis. Magnesium Bull. 1979; 1:46-48.

 

[13] Anghileri, L.J., Collery, P., Coudoux, P., Durlach, J. (Experimental

relationships between magnesium and cancer.) Magnesium Bull. 1981; 3:1-5

 

[14] Anghileri, L.J., Heidbreder, M., Weiler, G., Dermietzel, R.

Hepatocarcinogenesis by thioacetamide: correlations of histological and

biochemical

changes, and possible role of cell injury. Exp. Cell. Biol. 1977; 45:34-47.

 

[15] Blondell, J.W. The anticancer effect of magnesium. Medical Hypothesis

1980; 6:863-871.

 

[16] Whitney, R.B., Sutherland, R.M. The influence of calcium, magnesium

and cyclic adenosine 3'5'-monophosphate on the mixed lymphocyte reaction. J.

Immunol. 1972; 108:1179-1183.

 

[17] Petitou, M., Tuy, F., Rosenfeld, C., Mishal, Z., Paintrand, M.,

Jasmin, C., Mathe, G., Inbar, M. Decreased microviscosity of membrane lipids in

leukemic cells; two possible mechanisms. Proc. Natl. Acad. Sci. USA 1978;

75:2306-2310.

 

[18] Hass, G.M., McCreary, P.A., Laing, G.H., Galt, R.M.

Lymphoproliferative and immumunologic aspects of magnesium deficiency. In

Magnesium in

Health and Disease (from 2nd Intl Mg Sympos, Montreal, Canada, 1976), b Eds. M.

Cantin, M.S. Seelig, Publ. Spectrum Press, NY, 1980, pp 185-200

 

[19] Collery, P., Anghileri, L.J., Coudoux, P., Durlach, J. (Magnesium and

cancer: Clinical data.) Magnesium Bull. 1981; 3:11-20.

 

[20] American Journal of Epidemiology (Vol. 163, pp. 232-235)

 

[21] Journal of the American Medical Association, Vol. 293, pp. 86-89

 

[22] Mg2+ is critical for all of the energetics of the cells because it is

absolutely required that Mg2+ be bound (chelated) by ATP (adenosine

triphosphate), the central high energy compound of the body. ATP without Mg2+

bound cannot create the energy normally used by specific enzymes of the body

to make protein, DNA, RNA, transport sodium or potassium or calcium in and

out of cells, nor to phosphorylate proteins in response to hormone signals,

etc. In fact, ATP without enough Mg2+ is non-functional and leads to cell

death. Bound Mg2+ holds the triphosphate in the correct stereochemical

position so that it can interact with ATP using enzymes and the Mg2+ also

polarizes the phosphate backbone so that the ‘backside of the phosphorous’

is

more positive and susceptible to attack by nucleophilic agents such as

hydroxide ion or other negatively charged compounds. Bottom line, Mg2+ at

critical concentrations is essential to life,†says Dr. Boyd Haley who

asserts

strongly that, “All detoxification mechanisms have as the bases of the

energy required to remove a toxicant the need for Mg-ATP to drive the process.

There is nothing done in the body that does not use energy and without

Mg2+ this energy can neither be made nor used.†Detoxification of

carcinogenic

chemical poisons is essential for people want to avoid the ravages of

cancer. The importance of magnesium in cancer prevention should not be

underestimated.

 

[23] Magnesium has a central regulatory role in the cell cycle including

that of affecting transphorylation and DNA synthesis, has been proposed as

the controller of cell growth, rather than calcium. It is postulated that

Mg++ controls the timing of spindle and chromosome cycles by changes in

intracellular concentration during the cell cycle. Magnesium levels fall as

cells enlarge until they reach a level that allows for spindle formation. Mg

influx then causes spindle breakdown and cell division.

 

[24]

_http://www.nutraingredients.com/Research/Magnesium-may-be-key-to-calcium-s-canc\

er-benefits-study_

(http://www.nutraingredients.com/Research/Magnesium-may-be-key-to-calcium-s-canc\

er-benefits-study)

 

[25] Paunier, L., Radde, I.C.: Normal and abnormal magnesium metabolism.

Bull. of Hosp. for Sick Childr. (Toronto) 1965; 14:16-23.

 

[26] MAY 19, 1931, Dr. P. Schrumpf-Pierron presented a paper entitled “On

the Cause Of the Rarity of Cancer in Egypt,†which was printed in the

Bulletin of the Academy of Medicine, and the Bulletin of the French Association

for the Study of Cancer in July, 1931. _http://www.mgwater.com/rod02.shtml_

(http://www.mgwater.com/rod02.shtml)

 

[27] Yang CY et al. Jpn J Cancer Res.1998 Feb;89 (2):124-30. Calcium,

magnesium, and nitrate in drinking water and gastric cancer mortality.

 

[28] New York State Department of Health;

_http://www.health.state.ny.us/diseases/conditions/osteoporosis/qanda.htm_

(http://www.health.state.ny.us/diseases/conditions/osteoporosis/qanda.htm)

 

[29] Accu-Cell Nutrition; Calcium and Magnesium

_http://www.acu-cell.com/acn.html_ (http://www.acu-cell.com/acn.html)

 

[30] Am J Clin Nutr. 2007 Oct;86(4):1054-1063. Calcium requirements: new

estimations for men and women by cross-sectional statistical analyses of

calcium balance data from metabolic studies.Hunt CD, Johnson LK. US Department

of Agriculture, Agricultural Research Service, Grand Forks Human Nutrition

Research Center, Grand Forks, ND.

 

 

 

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