A Simple Natural Way of Reversing Malignant Process

At the end of the 19th century, Julius Cohnheim, a follower of Rudolf Virchow, arrived at an idea that cancer seemed to be “just an embryo cell, which was strayed”. Later, at the beginning of the 20th century, Alexander Maximoff, a Russian histologist, got the indirect evidence of existing reserve embryo cells. Then Otto Warburg, a Nobel Prize Laureate, discovered that cancer was caused by serious impaired cell respiration, which led to extremely intense lactic fermentation, for the cell needs energy to exist, and strong acidulation at the cellular level. 
As is well known, reserve embryo cells called also “vital cells” or “stem cells” were detected with the immunofluorescence method everywhere in the body. Their function is to make up for the loss of cells that underwent apoptosis (physiological cell suicide) as they were too old, as well as to make up for the loss of cells that underwent necrosis as they were sudden too damaged. Being immature cells, reserve embryo cells seem to be ultra vires of immune cells. Thus it seems to be impossible to bring the system of tissue regeneration under the control of the immune system. 

Today there is every reason to be of opinion that cancer tissue is a growing cell colony formed by the two populations of anaplastic cells (immature cells, which lost their orientation to one another). One of them is a large population of wrong immature cells and another is a small population of wrong reserve embryo cells, cancerous cells proper. The population of wrong reserve embryo cells has an excellent adaptation power because of chromosome aberrations. That is why carcinolytic therapy is basically false. In addition, being disorganized and hyperpermeable, cancer vessels are unable to maintain gradients between vascular and interstitial pressures. 
By Warburg’s research, the main problem of the wrong reserve embryo cell is permanent oxygen starvation, which leads to changing the activity of cell enzymes because of strong acidulation, and damage its mitochondria (cell power generators) with the byproducts of wrong oxidative phosphorylation. Thus we can allow that, when the wrong reserve embryo cell has mitotic failure (because of chromosome aberrations), its mitochondria destroyed too quickly. As a result, the wrong reserve embryo cell cannot supply the process of self-destruction with enough of energy and has to implement the program of necrosis.  
Now we have a reason to ask a question: can malignant process be reversed by preserving the mitochondria from necrosis during the process of cell self-destruction? It should be noted that the last is not very difficult biochemical problem. So some years ago I improved a good old method of treatment for pulmonary consumption trying to cure a small malignant tumor in the above way. As experience has shown, in the case of virgin cancer, which is in an initial stage, it is required only a few months to reverse the malignant process, and when the diagnosis is grounded on the quantification of cancer biomarkers only, it is required only a few months for complete recovery. 

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