Ottawa: In a paper published in the journal Cancer Prevention Research, researchers from McGill University and the University of Montreal have reported that exposure to metformin, a drug commonly prescribed to patients with Type II diabetes, reduces the cellular mutation rate and the accumulation of DNA damage. It is well known that such mutations are directly involved in carcinogenesis, but lowering cancer risk by inhibiting the mutation rate has never been shown to be feasible, according to the researchers.
In 2005, news first broke that researchers in Scotland found unexpectedly low rates of cancer among diabetics taking metformin. Many follow-up studies reported similar findings, some suggesting as much as a 50 per cent reduction in risk. The new study tried to explore how this anti-diabetic drug could reduce the risk of developing cancer and the mechanisms involved.
“It is remarkable that metformin, an inexpensive, off-patent, safe and widely used drug, has several biological actions that may result in reduced cancer risk – these latest findings suggest that it reduces mutation rate in somatic cells, providing an additional mechanism by which it could prevent cancer,” explains Dr Michael Pollak, professor in McGill’s departments of medicine and oncology, researcher at the Lady Davis Institute for Medical Research at the Jewish General Hospital and the study’s director.
The study, carried out in collaboration with the laboratory of Dr Gerardo Ferbeyre at the University of Montreal’s department of biochemistry, suggests that metformin reduces DNA damage by reducing levels of reactive oxygen species (ROS). ROS are known to be DNA-damaging agents produced as by-products when cells generate energy from nutrients. This action appears to take place in mitochondria, the cellular organelles that produce energy in cells by “burning” nutrients.
Past studies have identified the mitochondria as a site of action for metformin related to its anti-diabetic function, but those studies had not considered that the drug also acted here to reduce ROS production, thereby reducing the rate at which DNA damage accumulates. “We found that metformin did not act as a classic antioxidant,” says Dr Ferbeyre. “The drug seems to selectively prevent ROS production from altered mitochondria such as those found in cells with oncogenic mutations.”
“This study opens an exciting new direction in cancer-prevention research,” says Dr Pollak. “This doesn’t imply, however, that metformin is now ready to be widely used for cancer prevention. We do not yet know if the drug accumulates to sufficient concentrations in human tissues at risk for cancer, such as breast or colon, when taken at the usual doses used for diabetes treatment, nor do we know if the findings from the original studies showing reduced cancer risk, which were carried out in diabetics, also apply to people without diabetes. But the possibility of protecting DNA from oxidative damage by the use of a well-tolerated drug was not expected, and this topic now needs further study at many levels.”
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