Researchers have discovered a genetic deficiency in males that can trigger the development of one of the most common types of liver cancer and diabetes.
Michigan State University researchers found that when the NCOA5 gene, present in both men and women, was altered in male mice to a deficient level, a spontaneous reaction occurred producing cells that can lead to hepatocellular carcinoma, a type of liver cancer found to be two-to-four times more prevalent in men than women.
Findings also showed that prior to cancer development there were occurrences of glucose intolerance, a prediabetic condition that is believed to increase the risk of type 2 diabetes in humans.
Conversely, the study showed female mice did not develop these diseases.
"Essentially, what this provides is evidence for a genetic susceptibility in males to this particular type of liver cancer and diabetes," said Hua Xiao, lead researcher of the project and associate professor of physiology in MSU's College of Human Medicine.
"Ninety-four per cent of the male mice we looked at developed the liver cancer, while 100 per cent of these mice developed glucose intolerance," Xiao said.
Xiao noted the reason for the distinct outcomes between males and females also may have to do with the different levels of hormones between genders.
"Because estrogen may function through the NCOA5 gene and previously has been found to play somewhat of a protective role against both diseases, the result is a decreased risk in females," he said.
"Since males produce lower amounts of estrogen, this can contribute to their susceptibility," he added.
Type 2 diabetes has been widely associated with liver cancer as a common risk factor.
"At this point, it's not known if the genetic deficiency can be reversed and needs to be investigated further," Xiao said.
"But if it can somehow be changed through treatments such as drug therapies, this could substantially increase the chances of men in particular warding off these diseases," he said.
The research was published in the journal Cancer Cell.
