Another link to microorganisms, Fusobacterium this time.
When the researchers studied and compared healthy tissue and tumor tissue to each other, they found out that there was unusually large amounts of Fusobacterium's signature DNA in the tumor tissue.
"Tumors and their surroundings contain complex mixtures of cancer cells, normal cells, and a variety of microorganisms such as bacteria and viruses,"
"Over the past decade, there has been an increasing focus on the relationship between cancer cells and their 'microenvironment,' specifically on the cell-to-cell interactions that may promote cancer formation and growth." Source
Of course the researchers remain puzzled about the relationship of the microorganisms and tumors but if it talks like a duck and if it walks like a duck, oh well, I guess it has to be a duck
I have a feeling that it's these microorganisms that combine, alter or otherwise effect the cell''s DNA so that it loses control of itself and starts multiplying. Although this may be because of a natural immune defense, and a kind of designed procedure. The immune system is adjusting to the situation that there's an alien life form and it does the best it can. It tries to surround and capsulate the life form with cells, thus the tumor. I have considered this more in the lipoma genetics
There's also an unfamous Nobel Prize winner, Johannes Fibiger, who won his prize in 1926 in Physiology or Medicine. Atleast I have never herad from him.
He found out that microparasites could actually cause cancer.
...in the centre of the neoplasm he noted the presence of a worm belonging to the family of Spiroptera.
Fibiger did not succeed at first in proving a relationship existing between the formation of the neoplasm and the worm. The attempts to provoke a cancer in healthy mice by making them ingest neoplastic tissue from diseased mice, and containing worms or eggs, failed completely. Fibiger then had the idea that perhaps this worm, like many others, underwent part of its evolution from an egg to an adult individual in another animal, which served as an intermediate host. After numerous and vain attempts to find again mice attacked by the tumours seen in 1907 - he unsuccessfully examined more than 1000 animals - Fibiger eventually discovered in a sugar refinery in Copenhagen mice who exhibited in considerable numbers the type of tumour he was seeking; in these tumours he found once again the worm he had observed in 1907. The factory was at this time infested with cockroaches, and Fibiger was then able to establish that the worm in its evolution used these cockroaches as intermediate hosts. The cockroaches ingested the excreta of the mice, and with them the eggs of the worm. These developed in the alimentary tract of the cockroaches into larvae, which, like the trichina, were distributed into the muscles of the insects where they become encapsulated. The cockroaches were in their turn eaten by the mice and in the stomach the larvae transformed into the adult form. Source
Talking about some science fiction movie ideas!
Some more evidence to the parasite induced tumors are the facts that the cancer cells in vitro (in test tube) will not multiply without the addition of a growth factor, such as blood serum from calves and up to 96% of cancer cells have membrane-cell features.
That’s because cancer originates with infected membrane cells that receive epithelial growth factors from fungi or other parasites. Fungal infection of leukocytes (white blood cells) causes leukemia, but tumors do not form because leukocytes do not form membranes.
Bone cancer does not cause unrestrained bone growth because fungi do not produce bone growth factor. The same limitation applies to all organ tissue. Cancer consumes those cells that require growth factors fungi don't have. Fungi produce epithelial growth factor (EGG), like the skin of a mushroom, which can combine with human epithelial growth factor to mutate cell walls. New cells are unsuitable for performing their original function and are rejected like a skin graft that does not take. Fungi also produce bodies, like a mushroom, complete with arteries and veins as found in tumors formed by these mutated and rejected cells. All aspects of tumor growth have a fungal-based explanation.
Why we do not experience cancer of the heart, arteries or veins?
If cancer metastasizes through flowing blood, as we are told, we should have cancer in these tissues first. Why not? The high oxygen level in flowing blood destroys fermentative cells (cells extracting energy from the oxidation of organic compounds, such as carbohydrates, using an endogenous electron acceptor, which is usually an organic compound).
That’s why oxygen and ozone therapy,
banned in North America, can help prevent and cure cancer. Unrestrained growth of abnormal cells must stop if we eliminate the microbial source of growth factors in our body by eliminating all parasites. A herbal parasite cleanse program will help. Numerous effective cancer cures that reduce or eliminate infection, inflammation, toxins and pollutants are being ignored or suppressed while archaic methods that destroy the immune system and rapidly growing cells are permitted.
Destroying all rapidly growing cells with toxic drugs is a horrible medical mistake because it defeats the body’s only method to stop rapid cancer growth.
I borrowed and modified a lot from here
. There's also a nice explanation of how injuries trigger rapid and unrestrained tissue growth. I have had lipomas appeared to the spots of a trauma. It usually takes some months before the growth can be felt. I think currently that these parasites find their way to the trauma and inflammation locations and start producing growth factors, eat through membrane walls, infect adjacent cells, and initiate the current of injury.
The current of injury is an electric current generated when an injured part of a nerve, muscle, or other excitable tissue is connected through a conductor with the uninjured region; the injured tissue is negative to the uninjured.
Why aren't people born with cancer like the genetic Down's syndrome or why can identical twins get different diseases?
These ideas come mostly from the book called CANCER : Cause, Cure and Cover-up
in which the author presents a theory that parasitic growth factors initiate abnormal so-called “benign” growth and that the current-of-injury initiates unrestrained “malignant” growth. Must be a good book to read. Just ordered me a copy