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S c i e n t i f i c b a c k g r o u n d

The origin of the cancer cells and the artificial immune

system.

The 2015 nomination for the Nobel Prize in Physiology or Medicine is effective

to Coello Cedeno David I. For their discoveries concerning the biology of

cancer, in vitro processes induced carcinogenesis and the detailed study of

causing malignant transformation and a new prospect of the disease and where

comes in immunological processes antigen response - antibody. The work of

Nobel Prize nominee has revolutionized our understanding of the neoplastic

process. As a result of his discoveries, new fields of research have been

opened to keep the promise of improved treatments for cancer, infections and

other inflammatory diseases.

The discoveries

David Coello use Petri dishes and guinea pigs for preclinical trial in which he

realized that one of the quickest and most effective ways of producing cancer is

electromagnetism which submitted Petri dishes and in mice the process was

giving a milk diet and subjecting it to great waves of radiation so something

empirically with a microwave oven, something unorthodox but effective as he

demonstrated. In Petri dishes realized that the way in which cell cultures were

performed had time factor against and instability so that its effectiveness was

not guaranteed but a formulation with trypsin and plain agar under

electromagnetism provoked that to form an ideal synthetically entire human

metabolic process microenvironment is generated and its once all

immunological reactions give.

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Essays on the origin of cancer cells

To determine the metabolic development of cancer cells it is taken for a long

period of six months in which it needs the mouse to get the disease and a

breeding ground for cancer cells with which they can work with simple forms

analysis due to lack of materials and equipment for experiments.

Previously you could say, than normal cells ferment for yourself when you need

a reaction necessary to maintain homeostasis, which is false because the only

cells that ferment are damaged or cancerous because it is no longer regulates

herself due the failure of his breathing and invading microorganisms.

Studying the absolute fermentation of differentiated cancer cells from healthy

cells and what type cell fermentation need to enter in a precarious state and

thus to proliferate pathogens fiercely guests. What in laboratory work is done in

a quantitative way, I do it qualitatively. Because to understand cancer must

understand the fermentation.

It is generally understood especially the chemical mechanism of respiration and

fermentation, as it plays an important role in respiration and fermentation that

lead to reactions of engineering which will produce the energy needed for the

cell to live and thus will synthesized ATP which is a rich source of energy

produced by respiration and fermentation pathways which is necessary for life.

With cancer cells that occur in mice, for example, I have invented a way to see

the fermentation and cellular respiration by the decomposition of tissue in a

healthy mouse and another patient.

The decay time is the same eight hours to start the stench but the difference is

that in dissecting the sick mouse cell fermentation makes your fluids are acidic

and so learned in college know that in matters of Biochemistry this acid is

formed and this pH Lactic Acid acid was determined with litmus paper also

inflammatory reactions (pus) around the tumor lesion is observed.

In contrast to the healthy at the time of dissection mouse decomposition fluids

are alkaline which was determined by litmus paper.

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Which implies that when a result is given alkaline pH indicates that the tissue

was rich in oxygen. Liver and kidney of adult mouse is healthy or sick

dissections we realize by wear they had in their tone as these organs work

more than in that of a young animal, therefore consume more energy, which

can be Breath as fermentation.

When there is an injury in breathing, you can not increase the level of oxygen in

the animal's body at doses at which the body and the cells need because if he

dies.

It demonstrated when given air by gavage to sick animal which has led him

cancer that dies instantly, indicating therefore that oxygenation of the body and

damaged cells makes chemical reactions stop body to vary the pH of the blood

and the end result is the death of the animal. Therefore the oxygenation of the

cells is not possible because once damaged cellular respiration is no longer

returns to its original state.

A method for the destruction of cellular respiration is air pollution. In which mice

exposed to smoke from incense sticks every day for three months smoke and

carcinogenic chemicals that have gum stuck to the wood joins the incense

causes shortness of breath in the lungs to cause deficiency oxygen for a few

minutes and then place the mouse in a place without smoke, makes the

process of breathing normally destroys the lungs, and tend to form cancer as

dissection lungs are dark red in healthy animals, but in animals with cancer

lungs they turn black. The black color indicates positive (+) to cancer in all

irradiated organs.

The cause of this destruction of respiration is lack of energy. In fact, cells need

their respiratory energy to preserve their structure, and if respiration is inhibited,

cells suffer degenerations. No matter whether the oxygen is removed from the

cell or if the oxygen is prevented from reacting by a poison (smoke) in the

inhibition of respiration is also continuing through all subsequent cell divisions. I

think connection with its cellular respiration between these mitochondria

organelles explains carcinogenesis because a small part of the breathing takes

place in the fluid protoplasm and can be inhibited by a small radiation produced

by a microwave oven.

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Which I assume that the microwave radiation is from the inside out and

damaging breathing and damaged cells replicating, and this can be checked

with a histological examination. And if I use the microwave to accelerate cell

division in the mouse.

When cell respiration is irreversibly damaged, there is no 100% effective and

safe method for detecting cancer as tumor markers have a wide margin of error

and false-positive microorganisms that adhere to cancer cells that serve as

breeding ground for any germs, as these excreted toxins which alter tumor

markers.

For the formation of cancer is not only necessary to irreversible damage of

breathing also has to give an increase in the fermentation of fact, fermentation

strongly compensates for lack of breath.

The most important fact is that if there is an agent with which the fermentation

of cells in the body may increase with great speed but still takes a long time and

many cell divisions which are always necessary. To enhance fermentation in

the animal is made with the liver of healthy mice since it is known as liver cells

are cells that grow faster and are regenerated in the body.

It was it difficult to find a food that would cause an increase in liver cells

fermentation until I found this, and thus feed the mouse for 2 months with milk

and butter (the brand does not change the results, they remain the same) after

in which dissection note that some large tumors with infections occurred

because pus was found in the area because there was an inflammatory

response but could not determine the organism that produced it.

It should be noted that the pus is composed of white blood cells, dead cells,

glucose and fatty acids. With increasing glucose and final result of the

fermentation of glucose gives acidity, which makes it very resistant pus

inflammatory factor regardless of the place.

In the mouse the fermentation increase gradually in the course of days until it

formed a mass that was not normal in the liver of the animal.

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It is not known exactly from when the tumor occurred, inflammation and

infection but therefore I can only say that the time that increases the

fermentation and host infection is directly proportional to the damage of cellular

respiration.

This time differs in several animal rat mouse and guinea pig. So it is particularly

long in man because it occurs in the course of several decades.

Low energy deficiency in cells operating after the destruction of respiration

requires the cells to replace energy irrecoverably lost somehow breathing. This

occurs by a selective process that makes the cell and uses the fermentation of

cells to satisfy their energy needs.

Weaker cells in the fermentation die and not the strongest, and this selective

process continues until respiratory failure by higher fermentation and strongly

offset opportunistic infection.

Only then a cancer cell and a normal cell act which will move through the blood

system and may lead over time to metastasis.

The increase in fermentation takes a long time why it is only possible with the

help of many cell divisions. I also understand why the latency period is different

in mice and in humans depends on inflammatory reactions.

When cancer occurs in the abdominal cavity of the mouse contains many

cancer cells which induces by intake of sugar solution and already in their final

stages of life, the animal can not use its ability to breathe and ferment due to

lack of oxygen and excess sugar. However, cancer cells remain alive in the

abdominal cavity, even after the death of the mouse as in dissecting these

tissues are slow to decompose but are invaded by pus. This part also shows

that cancer cells require little energy.

This whole process induces immunosuppression body unable to remove

damaged cells and infection which is demonstrated in the accumulation of pus

found in dissections and a drop in the immune system which results from the

acidity caused by cells.

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Demonstration of artificial immune system reactions

The culture broths are made and added to the Petri and they are allowed to

harden in the refrigerator and then proceed to do this is sowing with oral

epithelial cells and more aseptic these crops were kept refrigerated overnight.

Petri dishes are placed in a location where they receive light, have plenty of air

flow (fresh) without moisture. Violently every day and observe the cells have

already formed a small tissue in all plates and allowed to stand.

Above each Petri dish two magnets one large and one small in order that the

following conditions are met cells were located:

Cells obtain ATP (energy) of O2 and glucose to damaged cell respiration O2 is

no deficit and no increase Glucose to maintain the level of energy (ATP)

balanced. Having magnets, electromagnetism, interrupts the entry of O2 and

this is demonstrated by acid pH and this is caused by the increase in glucose

fermentation

Following the basics of Bioenergetics, ATP in this case will be the same but in

the process will interfere electromagnetism magnets in their actions makes the

energy source of the O2 is replaced by Glucose since This is demonstrated in

the first signs of acidity and formation of small colonies of pathogens guests.

Fermentation is becoming stronger and feel the smell, no Putrefaction because

there is no color change of the culture broth or tissues, all are of normal color.

Keep in mind that all types of electromagnetism from the least like a magnet

damages the respiratory cycle of O2 and causes the pH acid becomes,

therefore, and I realized that the wave is more aggressive when it is smaller

because it takes a certain space, which can not only cause an induction to the

formation and proliferation of cancer cells, it can cause a number of diseases. In

which there are many issues for future research.

At days cell growth was observed in the agar suspension plus growing tissue,

also it is macroscopically observed proliferation and malignant transformation of

certain cells and tissues and an increase of fluids in a petri dish. Reactions

between the host and the microbe was also observed.

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In addition guests pathogenic microorganisms was observed which their quality

characteristics, and can say with certainty that microorganisms are protein

inducers of malignancies. Whether the tumors are similar to infections. And

these reactions produce inflammation (presence of pus).

Potential future effects of the Nobel Prize-Awarded discoveries in

clinical medicine

With all this research developed a large field of research aimed at more

effective and less toxic as it is very clear that any drug, regardless of Formula to

be able to cure cancer will aim Expand:

1. Be a Selective Cytostatic Action

2. Inhibitor of Microorganisms

3. Stimulating the immune system to the body to heal itself.

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The Nobel Assembly

The Nobel Prize in Physiology or Medicine is awarded by the Nobel Assembly, which consists of

50 professors at Karolinska Institutet. It meets 5 times per year, to discuss nominations for the

Prize, elect the Nobel Committee, and on the first Monday in October, to decide by vote who will

receive the Nobel Prize. Assembly members have to be professors at Karolinska Institutet and

remain on the Assembly as long as they are on its Faculty. When a seat is vacant, a new

member is elected by the Assembly.

Members of the Nobel Assembly 2015

Jan Andersson

Bo Angelin

Ernest Arenas

Per-Olof Berggren

Betsholtz

Ulf Eriksson

Patrik Ernfors

Forssberg

Jonas Frisn

Jesper Haeggstrm

Otherwise Hamsten

Gran K Hansson

Jan-Inge Loading

Richard Holmedahl

Christer Hoog

Carlos Ibez

Magnus Ingelman-Sundberg

Juha Kere

Be Kiehn

Torkel Klingberg

Classes Krre

Catharina Larsson

Nils-Gran Larsson

Katarina Le Blanc

Urban Lendahl

Hans-Gustaf Ljunggren

Lundberg, Jon

Maria Masucci

Monica Nistr

Nordberg

Magnus Nordenskjld

Pr Nordlund

Rolf Ohlsson

Tomas Olsson

Nancy Pedersen

Thomas Perlmann

Lorenz Poellinger

Annika Scheynius

Gunter Schneider

Camilla Sjgren

Edvard Smith

As Robbins

Jussi Taipale

Rune Toft Farm

Bjorn Vennstrm

Mats Wahlgren

Harriet Wallberg-Henriksson

Anna Wedell

Klas Wiman

Juleen Zierath

Chairman Bo Angelin

Deputy Chairman Rune Toftgrd Foro Nobel, Nobel vg 1, 171 77 Solna

Secretary Urban Lendahl Box 270 17177, Estocolmo

http://www.ki.se/The Nobel AssemblyMembers of the Nobel Assembly 2015