Researchers from in the Department of Microbiology and Immunology and UofL Health, James Graham Brown Cancer Center at the University of Louisville, have published an article which proposes a unique theory that a protein secreted by fat cells drives the development of breast cancer.
Associate professor, Dr Bing Li and colleagues have been conducting research funded by the National Cancer Institute for the past five years which led him to the connection between activity of a protein expressed in fatty tissue and an increase in breast cancer development. Li’s team and colleagues shared theor theory in an invited forum, ‘A New Player in Obesity-Associated Breast Cancer, in Trends in Molecular Medicine,. The article describes how adipose fatty acid binding protein (FABP4), expressed in fatty tissue, is responsible for fuelling breast cancer tumour growth.
"Many types of cancer are related to obesity, not only breast cancer. More than 13 types of cancer are clearly associated with obesity and I think the list will go on and on once we have more data," explained Li. "In our research, we found the fatty acid binding protein family, especially one member, FABP4, plays a very critical role in the association of obesity and cancer, most specifically breast cancer. We theorise that FABP4 is responsible for the underlying molecular mechanism which promotes obesity-associated breast cancer development."
Adipose tissue in the body produces FABP4 within fat cells, where it processes and distributes water-insoluble long-chain fatty acids. A certain amount of FABP4 enters the bloodstream under normal conditions. However, as a higher volume of fat tissue is accumulated, more FABP4 is secreted into circulation.
"When we get obesity, this protein is secreted out much more into the circulatory system," said Li. "Normally these molecules are inside the cells, but when people have obesity, the molecules are outside."
Li's theory offers two ways in which FABP4 may stimulate growth in breast cancer tumours.
First, within the cells, FABP4 increases in certain tumour-associated macrophages, which accumulate in tumours to promote tumour growth. Li's research also revealed that when FABP4 is inhibited, tumour growth is reduced in animal models even though the adipose tissue remained.
Second, when elevated levels of FABP4 circulate outside the fat cells in obesity, the protein promotes breast cancer development through direct interaction with breast cancer cells. In animal research, mammary tumour development and growth were reduced in obese animals in which FABP4 was controlled.
In addition, FABP4 in the bloodstream appears to work in multiple mechanisms to fuel interactions between tumour components and fat cells, thereby promoting cancer development.
Moreover, Li's research group recently published findings in Cancer Research showing that different types of high-fat diets have different effects on tumour development. High-fat diets of either cocoa butter or fish oil both result in fat-induced obesity. However, the cocoa butter diet results in increased mammary tumour growth, while the fish oil diet does not. This study not only confirms the critical role of FABP4 in obesity-associated cancer, but reveals that not all obesity promotes the development of tumours.
Li and his team believe a better understanding of how FABP4 works both within macrophages and in circulation could provide opportunities to prevent certain breast cancers from progressing. It may also lead to the development of treatment methods that target FABP4 with drugs or specific antibodies.
"Now we are trying to generate some antibodies for this protein, which could be a very effective therapy strategy for obesity-associated cancer," Li concluded.