Hi, all. Here's an interesting development. Dr. Michelakis at the U. of Alberta in Canada, who discovered that dichloroacetate (DCA) is effective against cancers in vitro and in mice a while back, has been able to test it in five humans with brain cancer, and it looks good. This could turn out to be pretty revolutionary for cancer treatment. DCA acts by forcing cancer cells, which operate by anaerobic metabolism, to revert back to aerobic metabolism, like normal cells, and then to die, like normal cells eventually do. Dichloroacetate is an old drug whose patent has run out, and the drug companies don't want anything to do with it for that reason. He had to pass the hat for contributions to test it, but he was able to raise the money, get approval from Health Canada, and now he has been successful in treating the first five human patients. Bravo! Best regards, Rich Dichloroacetate Effective Against Aggressive Brain Cancer Orphan drug dichloroacetate (DCA) has been found effective against aggressive brain cancer in a small Canadian study. Orphan drugs are meant to treat rare medical conditions. DCA is now used to treat a rare enzyme disorder in children, but researchers have found it useful in brain tumor too. The study published in Wednesday's online issue of the journal Science Translational Medicine showed tumours responded to DCA by changing their metabolism. Because DCA has a unique way of killing cancer cells, the new findings represent progress in a new area of cancer research that may stunt growth of tumours without harming healthy cells. “Solid tumors, including the aggressive primary brain cancer glioblastoma multiforme, develop resistance to cell death, in part as a result of a switch from mitochondrial oxidative phosphorylation to cytoplasmic glycolysis. This metabolic remodeling is accompanied by mitochondrial hyperpolarization. We tested whether the small-molecule and orphan drug dichloroacetate (DCA) can reverse this cancer-specific metabolic and mitochondrial remodeling in glioblastoma,” wrote Evangelos D. Michelakis of the University of Alberta and his colleagues. Freshly isolated glioblastomas from 49 patients showed mitochondrial hyperpolarization, which was rapidly reversed by DCA. In a separate experiment with five patients who had glioblastoma, they prospectively secured baseline and serial tumor tissue, developed patient-specific cell lines of glioblastoma and putative glioblastoma stem cells, and treated each patient with oral DCA for up to 15 months. There too the researchers tasted success. In four of the five glioblastoma patients, there was no further brain cancer growth after initial treatment. Follow-up studies on cells taken from these patients showed that DCA killed cancer cells. Nerve damage can occur at higher doses of DCA, but the study's authors suggest that at the dose used in the study, the drug might be able to stem tumor growth without serious side-effects. "We can conclude that DCA is possibly safe and maybe clinically effective in some patients," said Dr. Michelakis. "Due to the small size of this study we can't make more speculations. However, these early findings are enough to create enough enthusiasm and inspiration and momentum to go to the next step, which involves multi-centre trials." Funding for the Alberta University research was raised by a concerned community, apart from what could be obtained from federal agencies and from the university itself - pharmaceutical companies were not too keen on further research on DCA as it was a generic drug with no patent on it. "We challenged the dogma that without industry you can't actually test drugs on human beings," Michelakis noted with satisfaction. If researchers can understand how the tumour adapts its glucose metabolism to reap survival advantages, then DCA could be used in combination with other therapies to extend the lives of glioblastoma patients, Dr. Abhijit Guha, a professor of surgery at the University of Toronto, told CBC News. Currently, their average survival is 14 to 16 months with standard treatments.