[MOL] Important Information on Research of Enzymes in Specific Cancers [05990] Medicine On Line

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[MOL] Important Information on Research of Enzymes in Specific Cancers

Good Morning My Friends,

I just received this from a very knowledgable Doctor and thought this
might be of interest to you. I also have the list of those metabollic
doctors that you may wish to write to for further information.

God Bless
marty auslander

On  9 May 98 at 11:41,
GFoye <GFoye@aol.com> wrote:
> Months back there was a post by Cathey in reference to the need for enzymes
> to avoid cnacer. Not sure if it will help once cancer is established but
> would be a good expirement. I found Solaray Super Digestaway about closest
> to type enzymes suggested by Cathey. Problem is it will take a  month before
> any effects are noticed. I really believe  enzymes have a lot to offer
> providing they are the proper enzymes and taken in proper dosage. Contact R.
> Cathey for more info.

Roger Cathey posted the following, and it is a recurring theme which
to carry notable significance. I am including pancreatic (and digestive)
enzymes as one key component in my previously detailed treatment
I'm a firm believer -- and consequently recommend others *seriously*
doing the same.

Pancreatic enzymes, including amylase, trypsin, etc, are available from
various health stores; or Villa Park Pharmacy should be able to help.


Excerpted from below:
One thing certainly stands out: in every case of cancer pancreatic
enzymes are depressed.

Pancreatic enzymes are essential and central to the normal metabolically
mediated control and destruction of the cancer cell.

Thus the pancreatic deficiency becomes a vicious circle with very broad

Thus the complete metabolic protocol for cancer must always include the
pancreatic enzymes, especially amylase, whose role is to shear away the
surgery side chains attached to the proteins, and which give the cancer
cell it's strong negative charge that repulses the white blood cells;
trypsin, which degrades the proteins along with carboxypeptidase and
chymotrypsin; and later ribonuclease which degrades the cancer genome,
and lipase and probably all the other enzymes secreted by the pancreas,
and which enter the entero-pancreatic circulation. ...

Take care,

Date forwarded:   Mon, 23 Jun 1997 04:47:59 -0700 (PDT)
Date sent:        Mon, 23 Jun 1997 04:48:41 -0800
To:               rife-list@eskimo.com
From:             Robert Cathey Research Source <rcrs@europa.com>
Subject:          Re: Lung cancer--Long
Forwarded by:     rife-list@eskimo.com
Send reply to:    rife-list@eskimo.com

The story of Laetrile has few more dramatic successes than in the case
of lung
cancer. The case histories of the late Dr. John Richardson in treating
of lung and metastasized cancer to the lung were very good.  He utilized
metabolic protocol, including pancreatic enzymes, amygdalin, amino
acids, high
potency vitamins and minerals supplements, high dose retinoic acid
and emulsified or emulgated vitamin A to avoid the liver), high dose
vitamin C.

Dr. Philip Binzel can still be consulted,  who uses basically the same
protocols and whose results in a conservative estimate are 285% better
standard modalities in terms of life extension in his patients.  The
name of
his book, and phone number and that of other metabolic physicians is
at the end of this post, along with a partial bibliography. This paper
otherwise not referrenced.

We are preparing a description of an ideal rigorous protocol for
on our web site that will be referrenced, but in the mean time these
observations may be of help:

One thing certainly stands out: in every case of cancer pancreatic
enzymes are depressed. And as has also been proven true: whenever a
deficiency in function in one area is found in an organ, other functions
are often deficient as well.  So it is not surprising to find a higher
cancer incidence correlation in diabetics than in the rest of the

Pancreatic enzymes are essential and central to the normal metabolically
mediated control and destruction of the cancer cell.

Research has proven a correlation between chromium deficiency and the
decreased effectiveness of insulin as well as the digestive enzymes of
pancreas.  The insulin function is an endocrine function, while the
of enzymes are referred to as exocrine functions.  That the functional
products are both dependent on the mineral cofactor chromium further
up yet another aspect of metabolic disorder that attends both diseases:
diminished amino-acid metabolism.  Because it has been found that
assists in the delivery of amino acids to tissues and into cellular
This further explains the decline in the exocrine function, since the
exocrine pancreas can only synthesize the digestive enzymes when
amino acids are delivered. And chromium potentiates this function of
Thus the pancreatic deficiency becomes a vicious circle with very broad

Various reports are circulating that supplemental insulin dependency can
be dramatically reduced by satisfying the body's demand for chromium. In
experimental settings, when chromium is dialyzed out of the blood, it
been found that trypsin is only 5% as effective.  When the chromium is
returned, the enzymes regain their degrading power.  These findings were
proven in the 1950s in European labs.  It was therefore concluded that
chromium is a functional cofactor of trypsin, one of the primary
or proteolytic enzyme which is essential for the digestion of
proteins..including those in the cancer cell.

Trypsin is merely one member of a group of proteolytic enzymes secreted
the pancreas, and they all play a role in the degradation and
destruction of
cancer, along with the glycogen-digesting enzyme amylase. So important
is the
pre-action of these enzymes towards the resolution of cancer and other
disease systems, that the exocrine pancreas can justifiably be termed as
front line in the immune process.  Because not even the phagocytes--or
macrophages--can approach the cancer cell until these enzymes are
to do their work, due to an immune-cell repulsive coating around the

The best absorbed form of chromium is hexavalent chromate, which is
metabolized into tri-valent chromium or Glucose Tolerance Factor. Rich
sources of biologically active chromium are brewers yeast and black
pepper, as well as other readily available foods.  A super chromium
brewer's yeast is now manufactured for this biologically active metal.

When an enzyme degrades or breaks down a substance, the substrate, it's
called lysis.  In the early 1900s, Dr.s Mendell and Blood found that
hydrogen cyanide in the presence of proteolytic enzymes extended and
accelerated the activity of proteolysis as much as 300% and more.  At
that time it was not known that hydrogen cyanide could be delivered in a
metabolically non-toxic fashion from common food sources.  In the 1950s,
Ernst T. Krebs, Jr. positively correlated the intake of nitrilosides
(hydrogen cyanide bearing compounds found in many foods, mostly seeds)
with lower cancer incidence amongst aboriginal populations. Later, Dr.
Harold Manner and even the Memorial Sloan-Kettering proved the
anti-neoplastic action of nitrilosides in rats and mice.  Although the
MSK later recanted, the findings of Mendel and Blood alone suffice to
show a functional role for nitrilosides as a cofactor in the proper
function of pancreatic enzymes, just as chromium is.  But later Dr.
Manner and other clinicians proved the effectiveness of amygdalin in
human cancer. There are several papers in the RCRS Cancer index which
delineate some of these historical and clinical facts which go to prove
that along with chromium and other essential cofactors, nitrilosides are
functional cofactors as well.  For this reason the Krebses' and their
associates proposed these natural accessory food factors as a member of
the B vitamins or B-17, along with B-12, which also carries a nitrile or
cyanide as it's central molecule.

Thus research has shown that the numerous problems associated with
cancer as
well as the cancer itself, are symptoms of specific as well as
nutritional deficiencies, which formerly have often been grouped as
"paraneoplastic syndromes", rather than etiologically or cause-related
factors. Without an unifying principle to illuminate the nature of the
deficiencies, the universe of diverse facts surrounding cancer might
be trivialized or be inscrutable.

Interestingly, many so-called paraneoplastic syndromes relate directly
pancreatic function.  Consider the role of magnesium and it's
which researchers around the world recognize as having catastrophic
consequences in heart disease:  trypsin is secreted by the pancreas in
inactive form.  An enzyme called enterokinase (or enteropeptidase) is
required to activate trypsin (trypsinogen) and other enzymes secreted as
inactive from the pancreas referred to as "zymogens".  It is now
that the fall-off in the function of this intestinal activating enzyme
directly related to magnesium levels, as well as aging.  But magnesium
itself will activate trypsin, and therefore is an important adjunct not
only in the elderly who are the most frequent victims of cancer, but as
important cofactor in clinical intervention in cancer.  Magnesium is
to be essential in the activity of at least 70 different life-sustaining
enzymes in our bodies, and probably more.

The arrested development of certain white blood cells may be due to a
deficiency of trypsin, which I am told has been shown experimentally to
promote maturation of developmentally-arrested leukocytes.  That the
immune system functions only after the peri-cellular coating is digested
away from the cancer membrane is well established; if this leukocyte
development function can be fully confirmed, the pancreas must then be
termed an immune organ along with bone marrow and the thymus.

Thus the complete metabolic protocol for cancer must always include the
pancreatic enzymes, especially amylase, whose role is to shear away the
surgery side chains attached to the proteins, and which give the cancer
cell it's strong negative charge that repulses the white blood cells;
trypsin, which degrades the proteins along with carboxypeptidase and
chymotrypsin; and later ribonuclease which degrades the cancer genome,
and lipase and probably all the other enzymes secreted by the pancreas,
and which enter the entero-pancreatic circulation. (In multiple-myeloma,
amylase may not be required, as titers are usually high, while trypsin
inhibited, thus proving both enzymes are required for successful

There is strong empirical evidence that there is an absorption not only
of the intrinsic pancreatic enzymes back into the blood and lymph, but
also enzymes derived from our foods or supplements, as much as 40%
according to Dr.s Lopez, Williams, and Mielhke.

The principle concept is that cancer cells actually elicit pancreatic
proteases and amylase by their presence, just as food in the stomach
stimulates pancreatic secretion by means not fully understood.  A
deficiency in either amylase or the proteases would be disastrous if
continued unsatisfied.  The delivery of the essential amino acids,
chromium and magnesium (as well as zinc) insure that the pancreas will
synthesize these enzymes in sufficient quantity to satisfy both
intestinal digestion, and the immuno-enzyme function against the cancer
cell or parasites.

Supplemental enzymes at least insure that proteins delivered to the
stomach and intestines will go towards further synthesis. Supplemental
amino-acids are also utilized in the best metabolic clinics.  But as I
said, research indicates there is reabsorption of endogenous, and
absorption of exogenous enzymes, if not other macromolecules, which
will bolster the intrinsic enzymes by way of the entero-pancreatic

In many cases the only possibility of hope is direct injection of
and trypsin into the blood stream or lymph channels, as well as directly
the solid tumor or lesion.  The programs variously used follow closely
subjective responses, as well as presenting symptoms.  In most cases
injections have been well tolerated historically, but some clinics that
utilize parenterally administered enzymes allow a day of clearance

In lung cancer, the injection of the nitriloside amygdalin is especially
potent as it goes directly to the right heart, thence to the lungs and
avoids the liver altogether, where the hydrolized molecule may be
metabolized into less active form.  Even after metabolization, however,
the thiocyanate metabolite will accelerate proteolysis.


What is the unifying principle then? Cancer cells are normal cells to
the life
cycle, and their principal role is in pregnancy as the origin of the
amnion and chorion both, wherein they are known as trophoblasts. Thus
they are
equipped with several defensive maneuvers to survive in the autonomous
they play in the fetal nutrition.  They are a potentiality of the
or "individual" cell, the germ cell, originally activated by sex
And after they develop, they also secrete hormones and steroids for
further development and preservation.  The mother reacts to this
cancer system, or the trophoblasts by secreting digestive enzymes.

The trophoblast must defend itself against these enzymes, and so it
secretes inhibitors which deactivate these enzymes.  A similar mechanism
is used by pin and round worms like Ascaris, and other parasites.  The
chorionic trophoblasts succeed at this inhibition for about 8 weeks,
there is a sudden fall off in the activity of the invasive and
trophoblast (cytotrophoblast).  Why?  At the 8th week, the fetal
begins to function, and so it contributes proteolytic enzymes to the
degradation of the diffusing hormones or proteins of the
system. Still, it takes a further 28 months of continual, daily enzyme
to fully control and destroy the trophoblasts.

Actually the cancer (trophoblast) cell first becomes transformed by
enzymes into a non-dividing, steroid producing phase, which corresponds
so-called benign, non-proliferating, or non-dividing cancer, or
processes. They still expand slightly by actually fusing with the
somatic elements or normal cells of the mother's uterus, which results
multi-nucleated, highly vascularized cellular processes.
 If the pancreatic enzymes don't actually over-balance the output of the
enzyme-inhibitors of the trophoblasts, the former cyto-trophoblast can
re-arise, with powers of division and metastasis and then you have a
fulminating chorionepithelioma, the deadliest cancer there is.

Thus the complete degradation of the trophoblasts of pregnancy
a complete "regression" in cancer.  Every living human being represents
conquering of cancer. And after birth not one such trophoblast is left
in the infant's body.  Trophoblast is the origin of the entire placenta,
does not become incorporated into the living form.

But various competent cells do exist within us, male and female, that
evolve into trophoblast and not just germ cells. It invariably begins
estrogen or an estrogen-like carcinogen. The hybridization of
with the tissues of the primary site is what gives the wide variety of
of cancer. But trophoblast is the constant malignant component, as is
by the several proteins expressed by cancer which are shared only with


The commonest enzyme inhibitors might be running out of your tap: heavy
metals like copper, mercury and silver.  They are certainly ubiquitous
the industrialized environment.  But even sweet potatoes and soy beans,
properly cooked, can inhibit trypsin.  We aren't certain, but we believe
canola or rape-seed oil, one of the most processed oils on the market,
inhibit trypsin and possibly lipase, tests are under way. Margerine can
up the works, so butter is preferred. Organic foods are of course best.
organophosphates commonly used in pesticides are amongst the most
of the inhibitors, broadly referred to as serpins.  For heavy metals,
N-acetylcysteine, EDTA, and other chelators are important.

As mentioned, intestinal parasites like ascaris secrete trypsin
inhibitors, and so pains should be taken to follow some anti-parasitical
protocols. Laetrile or amygdalin is believed to be a good parasiticide,
vermifuge or anthelmintic. Ficin was shown to dissolve ascaris even when
trypsin failed to do so (ficin is derived from fig sap, is used diluted,
and is found to some extent in yellow figs).  Papain and bromelain
together with fig-factor and nitrilosides are bound to purge many
parasites.  Fluttering in the liver area may indicate liver flukes or
other cestodes.

If chelation is resorted to, there must be followed a rigorous repletion
program for calcium, chromium, magnesium and zinc especially, as these
essential for enzyme attachment and optimal conformation in degrading
cancer-membrane-substrates.  Orotates are the preferred organic-metals,
for chromium, yeast-GTF, or tri-valent chromium-nicotinate.

Vitamin A has been noted to be essential for normal differentiation of
epithelium, which by far is the most frequent tissue target for cancer
evolution.  Vitamin A deficiency leads to squamous cellular processes,
and metaplasia, which is frequently observed to be a precursor in cancer
evolution. Beyond that, it has been noted that amongst the side-effects
retinoids (primarily synthetic retinoids, due to the toxicity of natural
analogs) is a weakening of the lysomal membranes in the cancer cells,
can lead to autolysis or slow the cancer cell down at least, since the
movement of these internal enzymes to the outside of the cancer cell for
destruction of tissues might be more difficult if the membrane is
Clinical experience shows that as high as 500,000 units of emulsified
vitamin A is well tolerated if gradually introduced.

The experience with immuno-enzyme therapy and vitamin A is probably the
most well documented in European clinics.  Megadoses of vitiman A were
observed to stimulate the immune response, cellular antibody formation
especially. Some of the side effects of this in conjunction with enzymes
are inflammatory reactions of latent infections, but they normally
subside in 2 or 3 days.

That's it.  As short as can be said without leaving out essential facts.
Here is a list of metabolic physicians who satisfy every point of this
outline.  Remember, if a trained physician is a fool to treat
himself....what to say of the untrained?  Get expert help. Expert and
experienced metabolic physicians. Don't make any mistake.
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