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From www.wikipedia.org
Dichloroacetic acid, often abbreviated DCA, is a chemical compound, an acid, and an analogue of acetic acid in which two of the three hydrogen atoms of the methyl group have been replaced by chlorine atoms, it has the chemical formula CHCl2COOH. The salts and esters of dichloroacetic acid are called dichloroacetates.

Chemistry and occurrence
The chemistry of dichloroacetic acid is typical for halogenated organic acids. It is a member of the chloroacetic acids family. The dichloroacetate ion is produced when dissolved in water. As an acid with a pKa of 1.48,[4]
pure dichloroacetic acid is very corrosive and extremely destructive to
tissues of the mucous membranes and upper respiratory tract.[5]
DCA does not occur in nature. It is a trace product of the chlorination of drinking water and is produced by the metabolism of various chlorine-containing drugs or chemicals.[6] It is typically prepared by the reduction of trichloroacetic acid.
Therapeutic use
Owing to the highly corrosive action of the acid, only the salts of dichloroacetic acid are used therapeutically, including its sodium and potassium salts, sodium dichloroacetate and potassium dichloroacetate.
Lactic acidosis
The dichloroacetate ion stimulates the activity of the enzyme pyruvate dehydrogenase by inhibiting the enzyme pyruvate dehydrogenase kinase.[7] Thus, it decreases lactate production by shifting the metabolism of pyruvate from glycolysis towards oxidation in the mitochondria. This property has led to trials of DCA for the treatment of lactic acidosis in humans.[8][9][10][11]
A randomized controlled trial in children with congenital lactic acidosis found that while DCA was well tolerated, it was ineffective in improving clinical outcomes.[9] A separate trial of DCA in children with MELAS (a syndrome of inadequate mitochondrial function, leading to lactic acidosis) was halted early, as all 15 of the children receiving DCA experienced significant nerve toxicity without any evidence of benefit from the medication.[10]
A randomized controlled trial of DCA in adults with lactic acidosis
found that while DCA lowered blood lactate levels, it had no clinical
benefit and did not improve hemodynamics or survival.[11]
Thus, while early case reports and pre-clinical data suggested that
DCA might be effective for lactic acidosis, subsequent controlled
trials have found no clinical benefit of DCA in this setting. In
addition, clinical trial subjects were incapable of continuing on DCA
as a study medication owing to progressive toxicities.

Potential cancer applications
Cancer cells generally use glycolysis rather than respiration (oxidative phosphorylation) for energy (the Warburg effect), as a result of hypoxia that exists in tumors and damaged mitochondria.[12] Usually dangerously damaged cells kill themselves via apoptosis, a mechanism of self-destruction that involves mitochondria, but this mechanism fails in cancer cells.
A study published in January 2007 by researchers at the University of Alberta,[13] testing DCA on in vitro
cancer cell lines and a rat model, found that DCA restored
mitochondrial function, thus restoring apoptosis, killing cancer cells in vitro, and shrinking the tumors in the rats.[14]
These results received extensive media attention, beginning with an article in New Scientist titled "Cheap, ‘safe’ drug kills most cancers".[15] Subsequently, the American Cancer Society and other medical organizations have received a large volume of public interest and questions regarding DCA.[16] Reports have since pointed out that although the study results are promising, no formal clinical trials
in humans with cancer have yet been conducted in the USA and are not
yet final in Canada, emphasizing the need for caution in interpreting
the preliminary results.[16][17]
Some doctors are treating cancer using DCA "off-label",[18][19] which generates controversy in some circles.[18] The off-label use
of prescription drugs is common practice for cancer patients at the
most prestigious medical institutions in the world, especially those
diagnosed with cancers designated as orphan diseases, for which very few government-approved therapies are available. For example, to treat the grade IV brain cancer called glioblastoma, UCLA Neuro-oncology uses some 50 different drugs, only 4 of which are currently FDA-approved to treat glioblastoma.[20] Oral DCA, which has been safely used to treat lactic acidosis for more than 30 years in humans[14] (but see above), is currently in human clinical trials for glioblastoma.[21]
Drs. Akbar and Humaira Khan have since March 2007 treated cancer
patients using DCA off-label at their private clinic, Medicor Cancer
Centres, in Toronto.[22]
They have treated several types of cancer and said on their web site
that some patients "are showing varied positive responses to DCA
including tumour shrinkage, reduction in tumour markers, symptom
control, and improvement in lab tests".[19]
Although, they have not published their results nor reported it at
medical conferences, they have uploaded details of patient responses
and overall statistics on their web site. [23]
Dr. Terry Polevoy, of Kitchener, Ontario, called on the College of
Physicians and Surgeons of Ontario to take away the Khans' licences for
offering a compound that hasn't been proven to shrink tumours in
humans. "They are not oncologists. They should not be making these
decisions. I think they should be disciplined for using this stuff.
That, to me, is unethical, to use something that has never been proved
to do anything." But the College said that it was not their role to say
which therapies a doctor can use.[24]
Dr. Polevoy himself is not an oncologist, but a medical doctor who runs
an acne clinic in Kitchener, Ontario, as well as a web site devoted to
exposing what he considers self-promotion and self-described "quack
remedies" called Healthwatcher.net[25].
The New Scientist later editorialized, "The drug may yet live
up to its promise as an anti-cancer agent – clinical trials are
expected to start soon. It may even spawn an entirely new class of
anti-cancer drugs. For now, however, it remains experimental, never yet
properly tested in a person with cancer. People who self-administer the
drug are taking a very long shot and, unlikely as it may sound, could
even make their health worse."[26]
DCA has been used historically to treat patients with lactic
acidosis, and therefore could arguably enter phase 2 trials in patients
with cancer.[27]
DCA is non-patentable as a compound, though a patent has been filed for its use in cancer treatment.[28] Research by Dr. Evangelos Michelakis has received no support from the pharmaceutical industry.
Concerns have been raised that without strong intellectual property
protection, the financial incentive for pharmaceutical industry
interest is reduced, and therefore clinical trials of DCA may not be
funded.[15][16][17][29] However, other sources of funding exist; previous studies of DCA have been funded by government organizations such as the National Institutes of Health, the Food and Drug Administration, the Canadian Institutes of Health Research and by private charities (e.g. the Muscular Dystrophy Association).
Recognizing anticipated funding challenges, Dr Michelakis's lab took
the unorthodox step of directly soliciting online donations to fund the
After 6 months, his lab had raised over $800,000, enough to fund a
small Clinical Phase 2 study. Dr. Michelakis and Dr. Archer have
applied for a patent on the use of DCA in the treatment of cancer.[31][32]
On 24 September 2007,
the Department of Medicine of Alberta University reported that after
the trial funding was secured, both the Alberta local ethics committee
and Health Canada approved the first DCA Clinical Trial in Cancer.[33] This initial trial is relatively small (enrollment- up to 50 patients in the following 18 months).
The promise of DCA as a cheap, effective and safe treatment for
cancer generated a great deal of public interest. Many people turned to
self-medication. [34][35]
When faced with the high costs of getting Food and Drug Administration approval, estimated by Tufts University to exceed one billion dollars [36],
the chance of getting DCA approved for the treatment of cancer in the
United States is extremely low. This problem is highlighted in the 2007
New York Times article by Ralph Moss titled "Patents over Patients" [37].
Side effects
Reports in the lay press after the 2007 University of Alberta announcement claim that dichloroacetate "has actually been used safely in humans for decades",[38] but the limited scholarly literature suggests side effects of pain, numbness and gait disturbances in some patients.[38] A clinical trial where DCA was given to patients of MELAS (a form of genetically inherited lactic acidosis) at 25 mg/kg/day was ended prematurely due to excessive peripheral nerve toxicity.[39] Dichloroacetate can also have anxiolytic or sedative effects.[6]
Animal studies suggest that the neuropathy and neurotoxicity during chronic dichloroacetate treatment may be partly due to depletion of thiamine, and thiamine supplementation in rats reduced these effects.[40]
However, more recent studies in humans suggest that peripheral
neuropathy is a common side effect during chronic DCA treatment, even
with coadministration of oral thiamine.[41][42]
An additional study reported that 50 mg/kg/day DCA treatment resulted
in unsteady gait and lethargy in two patients, with symptoms occurring
after one month for one patient and two months for the second. Gait
disturbance and consciousness were recovered with cessation of DCA,
however sensory nerve action potentials did not recover in one month.[43]
Studies of the trichloroethylene (TCE) metabolites dichloroacetic acid (DCA), trichloroacetic acid (TCA), and chloral hydrate suggest that both DCA and TCA are involved in TCE-induced liver tumorigenesis and that many DCA effects are consistent with conditions that increase the risk of liver cancer in humans at dosages much higher than used for cancer therapy.[44]
It has been reported that animals and patients treated with DCA have elevated levels of delta-aminolevulinic acid
(delta-ALA) in the urine. A study published in 2008 suggests that this
product may be the cause of the neurotoxic side-effect of DCA by
blocking peripheral myelin formation. ([1])

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