Scientists cure cancer but no one takes notice
Cheap, 'safe' drug kills most cancers
Cancer cell
Positron emission tomography (PET) imaging has now confirmed that most malignant tumors have increased glucose uptake and metabolism. This bioenergetic feature is a good marker of cancer but has not been therapeutically pursued, as it is thought to be a result and not a cause of cancer; that is, the cells rely mostly on glycolysis for energy production because of permanent mitochondrial damage, preventing oxidative phosphorylation. However, whether the mitochondria in cancer are indeed damaged and whether this is reversible remain unknown. (http://www.sciencedirect.com/science/article/pii/S1535610806003722)
DCA in the drinking water at clinically relevant doses for up to 3 months prevents and reverses tumor growth in vivo, without apparent toxicity and without affecting hemoglobin, transaminases, or creatinine levels. The ease of delivery, selectivity, and effectiveness make DCA an attractive candidate for proapoptotic cancer therapy which can be rapidly translated into phase II-III clinical trials. (http://www.sciencedirect.com/science/article/pii/S1535610806003722)
Note:Text and pictures were thankfully shared from their original sources as listed below:
Canadian scientists (metabolic modulation of glioblastoma with dichloroacetate) tested this dichloroacetate (DCA) on human's cells;
it killed lung, breast and brain cancer cells and left the healthy cells
alone. It was tested on Rats inflicted with severe tumors; their cells
shrank when they were fed with water supplemented with DCA. The drug is
widely available and the technique is easy to use, why the major drug
companies are not involved? Or the Media interested in this find?
Cheap, 'safe' drug kills most cancers
It sounds almost too good to be true: a cheap and simple drug that kills
almost all cancers by switching off their "immortality". The drug,
dichloroacetate (DCA), has already been used for years to treat rare
metabolic disorders and so is known to be relatively safe.
DCA attacks a unique feature of cancer cells: the fact
that they make their energy throughout the main body of the cell,
rather than in distinct organelles called mitochondria. This process,
called glycolysis, is inefficient and uses up vast amounts of sugar.
Until now it had been assumed that cancer
cells used glycolysis because their mitochondria were irreparably
damaged. However, Michelakis's experiments prove this is not the case,
because DCA reawakened the mitochondria in cancer cells. The cells then
withered and died (Cancer Cell, DOI: 10.1016/j.ccr.2006.10.020).
Michelakis suggests that the switch to glycolysis as an energy source
occurs when cells in the middle of an abnormal but benign lump don't get
enough oxygen for their mitochondria to work properly. In order to survive, they switch off their mitochondria and start producing energy through glycolysis.
Crucially, though, mitochondria do another job in
cells: they activate apoptosis, the process by which abnormal cells
self-destruct. When cells switch mitochondria off, they become
"immortal", outliving other cells in the tumour and so becoming
dominant. Once reawakened by DCA, mitochondria reactivate apoptosis and
order the abnormal cells to die.
"The results are intriguing because they
point to a critical role that mitochondria play: they impart a unique
trait to cancer cells that can be exploited for cancer therapy," says
Dario Altieri, director of the University of Massachusetts Cancer Center
in Worcester.
The phenomenon might also explain how
secondary cancers form. Glycolysis generates lactic acid, which can
break down the collagen matrix holding cells together. This means
abnormal cells can be released and float to other parts of the body,
where they seed new tumours.
Cancer cell
Cancer progression and its resistance to treatment depend, at least in
part, on suppression of apoptosis. Although mitochondria are recognized
as regulators of apoptosis. In
1930, Warburg suggested that mitochondrial dysfunction in cancer results
in a characteristic metabolic phenotype, that is, aerobic glycolysis (Warburg, 1930).
picture courtesy:http://www.sott.net/article/ 228583-Scientists-cure-cancer-but-no-one-takes-notice |
Positron emission tomography (PET) imaging has now confirmed that most malignant tumors have increased glucose uptake and metabolism. This bioenergetic feature is a good marker of cancer but has not been therapeutically pursued, as it is thought to be a result and not a cause of cancer; that is, the cells rely mostly on glycolysis for energy production because of permanent mitochondrial damage, preventing oxidative phosphorylation. However, whether the mitochondria in cancer are indeed damaged and whether this is reversible remain unknown. (http://www.sciencedirect.com/science/article/pii/S1535610806003722)
Cancer mitochondria are hyperpolarized and have suppressed oxidative metabolism, both of which are reversed by DCA
The small molecule DCA is a metabolic modulator that has been used in humans for decades in the treatment of lactic acidosis and inherited mitochondrial diseases. Without affecting normal cells DCA reverses the metabolic-electrical remodeling, inducing apoptosis and decreasing tumor growth.
picture courtesy:http://www.sciencedirect.com/ science/article/pii/S1535610806003722 |
DCA in the drinking water at clinically relevant doses for up to 3 months prevents and reverses tumor growth in vivo, without apparent toxicity and without affecting hemoglobin, transaminases, or creatinine levels. The ease of delivery, selectivity, and effectiveness make DCA an attractive candidate for proapoptotic cancer therapy which can be rapidly translated into phase II-III clinical trials. (http://www.sciencedirect.com/science/article/pii/S1535610806003722)
Paul Clarke, a cancer cell biologist at the University of Dundee in the
UK, says the findings challenge the current assumption that mutations,
not metabolism, spark off cancers. "The question is: which comes first?"
he says.
Note:Text and pictures were thankfully shared from their original sources as listed below:
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