Chemotherapy can improve melanoma development by damaging the DNA of close by healthier tissues. Researchers found "evidence of DNA damage" in healthier tissues after radiation therapy treatment. Researchers recently published this report in Nature Medication.
Cancer tissues process glucose differently than do healthier tissues. Cancer tissues cannot process fresh air like healthier tissues and it is this low fresh air level that shows to be the key factor in melanoma development.
Most tissues and most necessary protein in blood are glycosylated; that is, they are covered with carbs. This covering of glycoprotein receptor websites form the os (OS) for your tissues and one's individual body communication program including translating and transcription DNA.
The broken DNA turns on the healthier tissues to discharge a necessary protein that gets growth development and cause level of ability to resist further radiation therapy. The broken DNA demands WNT16B necessary protein which is then used to boost the melanoma mobile success.
Other research that fermentation of glucose, because of lack of fresh air, allows the tissues of melanoma to lose all beneficial function. Cancer with the biggest fermentation amount has the biggest amount of development producing only putrid harmful waste because the mobile cannot process further without fresh air.
The WNT16B research was seeking to explain why melanoma tissues are so simple to kill in the lab, yet so strong inside one's individual body program. Healthy tissue gathered from men with prostate melanoma showed proof of DNA harm following radiation therapy. The team verified and then reconfirmed their results with breast and ovarian melanoma cancers. Co-author of the research, Chris Nelson of the Sam Hutchinson Cancer Research Center in Dallas stated, "The improve in WNT16B was absolutely surprising." These results were "completely unexpected".
Nelson explained, "WNT16B (protein), when produced, would interact with close by growth tissues and cause them to grow, get into, and importantly, avoid following therapy."
Tumors often respond well with radiation therapy initially; but, is normally followed by rapid growth, prior to developing level of ability to resist further therapy. Oncologists know this danger; but now they know why: the WNT16B necessary protein.
Cancer tissues crave glucose. Sugars that are super simple to ferment feed melanoma while some Intelligent Sugars avoid melanoma and build a powerful immune immune program.
My concepts is that melanoma tissues "mow down glycoproteins " on the surface of nearby tissues, thus decline or eliminating their signaling abilities. This reverse glycosylation (stripping away the glycoprotein receptor sites) leaves the mobile undressed and helpless, unable to call for help to correct the situation. It cannot receive the care and feeding, so melanoma propagates as it produces a more acid/toxic environment.
Smart Sugars coat healthier tissues like felt on a peach; however, melanoma tissues are depleted of glycoproteins. Healthy tissues have a woodlands of glycoproteins while melanoma tissues are gap of this living woodlands.
The future of drugs and healthcare is in analyzing glycoproteins by literally counting and determining the quality of these receptor websites. Healthcare science will gather planets of data through the soon to be Gold Standard of medical diagnostics to determine if the tissues are healthier, bald, or baldness.
The age-old question is: "Is the cup 50 percent full or 50 percent empty?" Is that really important? Just fill the glass!" Do we treat the melanoma, enable the melanoma, or prevent the presence of melanoma simply by growing more glycoprotein receptor websites. We now have scientific proof that oral consumption of Intelligent Sugars can and do improve glycosylation in the individual body.
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