image: This image shows intestinal stem cells (green) and fatty acids (red) in the intestine of mice. Intestinal stem cells can self-renew and they fuel complete turnover of the intestinal lining every three to five days. Fatty acids are an important nutrient source for the self-renewal of intestinal stem cells. view more
Credit: Lei Chen
Two genes that appear to help stem cells in the intestine burn dietary fat may play a role in colon cancer, according to a Rutgers study.
The study, published in the journal Gastroenterology, describes a new connection between the way cells consume fat and how genes regulate stem cell behavior in the intestines of mice.
"This is important because scientists have shown that when there's too much dietary fat in the intestine, stem cell numbers increase, boosting susceptibility to colon cancer," said senior author Michael Verzi, an associate professor in the Department of Genetics in the School of Arts and Sciences at Rutgers University-New Brunswick. Verzi is also a research member in the Genomic Instability and Cancer Genetics Research Program at Rutgers Cancer Institute of New Jersey.
People naturally lose millions of intestinal cells daily, much like they lose skin cells. Intestinal stem cells undergo constant renewal and fuel the continuous turnover of the lining of the intestine, but altered stem cell functions can lead to colon cancer.
Colorectal cancer (of the colon or rectum) is the third most common cancer diagnosed in both men and women in the United States. An estimated 101,420 Americans will be diagnosed with colon cancer this year, according to the American Cancer Society.
Recent studies have shown that intestinal stem cells can increase in animals on a high fat "Western" diet, potentially explaining an elevated cancer risk from such a diet.
The Rutgers team recently discovered that two genes (HNF4A and HNF4G) work together to promote the proper function of the intestinal lining. In the new study, they found that mice lost intestinal stem cells when these genes were inactivated, confirming their importance. Rutgers scientists believe that the genes help stem cells burn fat, providing them energy.
Going forward, the researchers hope to further investigate whether the two genes alter stem cell numbers and cancer risk during a high fat diet, said Verzi, who is also a member of the Rutgers Center for Lipid Research.
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The lead author is Lei Chen in Verzi's lab. Rutgers co-authors include Roshan P. Vasoya, Natalie H. Toke, Aditya Parthasarathy and Shirley Luo in Verzi's lab; Eric Chiles at the Rutgers Cancer Institute of New Jersey; graduate student Juan Flores, Associate Professor Nan Gao and Professor Edward M. Bonder in the Department of Biological Sciences at Rutgers-Newark; and Assistant Professor Xiaoyang Su at the Rutgers Cancer Institute of New Jersey and Department of Medicine at Rutgers Robert Wood Johnson Medical School in Rutgers Biomedical and Health Sciences.
Journal
GASTROENTEROLOGY