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| Thomas Seyfried |
According to Seyfried, cancer begins in the mitochondria. The main evidence of his theory is dysfunctional mitochondria. Electron microscopic photographic images clearly show damaged mitochondira in many but not all cancers. This results in fermentation (glycolysis and glutaminolysis) for energy even when oxygen is present. Tumor growth depends heavily on specific fuels like glucose and glutamine; depriving cells of these fermentable fuels through restricted ketogenic diets or metabolic therapies targets cancer cell survival. The main advantage of the Ketogenic Metabolic Therapy is that it does not damage non-cancerous cells because healthy cells have flexible, fully functioning mitochondria that can switch to burning fats and ketones for energy, whereas cancer cells rely rigidly on fermentation (glucose and glutamine) and lack this metabolic flexibility.
His critics point out that thousands of peer-reviewed genomic studies show specific, recurring driver mutations (such as in TP53, BRCA, or EGFR) that directly cause uncontrolled cell growth. Indeed, I found his ignorance (?), omission or dismissal of genetic evidence rather shocking. He has the right to have an alternative theory, but he must deal with the established mainstream facts [1]. You can't just ignore them. It is very unlikely that the association of specific 'cancer mutations' and cancer are accidental and have no meaning. What is the likelihood that a mere handful out of the 25,000 human genes would acquire mutations so consistently in almost all cancers? How do cancer-specific mutations arise as an epiphenomenon of the 'disturbance of cellular energy metabolism'?
Another question I have is: What is the cause of dysfunctional mitochondria? Could it be that this is caused by mutations in mitochondrial-DNA or in nuclear-DNA? Seyfried should address these matters especially if he wants to be taken serious by mainstream science. Furthermore, I wonder why dysfunctional mitochondria result in uncontrolled cell division. Why should that have survival advantage? Why don't those cells just die? This is an unsolved problem in his theory [2].
Seyfried is a scientific maverick in the sense that he is an independent and unorthodox researcher and an outspoken critic of mainstream oncology. He accuses mainstream oncologists of dogmatism and 'confirmation bias'. The reason that I blogged about Seyfried is that he has alternative views (I am always interested in interesting alternative views!) and that he is strongly opposed to dogmatic DNA- and gene-centric thinking. Finally, Seyfried's therapy could render harsh treatments such as chemotherapy and radiation unnecessary, and potentially save lives.
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