Cancer treatments could evolve from research showing that acetate supplements speed up cancer growth
UT Southwestern Medical Center researchers seeking novel ways to combat cancer found that giving acetate (a major compound produced in the gut by host bacteria) to mice sped up the growth and metastasis of tumors.
Bacteria living inside the gut can have beneficial, but potentially also harmful effects on human health. Further studies are needed to determine whether restricting acetate production by gut bacteria will affect growth of tumors.
“With insights generated from our current studies, we may be able to design therapies that treat cancer patients by modulating acetate production in the body,” said Dr. Joseph Garcia, Associate Professor of Internal Medicine at UT Southwestern and staff physician-scientist at the VA North Texas Health Care System.
The work is published in the February issue of the journal PLOS ONE.
Cancer, the second leading cause of death in the US, is estimated to account for nearly 1 out of every 4 deaths in 2014. It can have a significant impact on length and quality of life, which carries a tremendous economic burden. Cancer can develop in any part of the body and some are notoriously difficult to treat, although recent discoveries from basic science laboratories hold great promise for more effective treatments and potential cures.
In cancer cells, low oxygen and low glucose conditions turn on signaling pathways that allow otherwise healthy cells to survive these stresses. UT Southwestern researchers previously discovered a critical pathway that controls the response of cells and organs to low oxygen conditions, a state known as hypoxia. In this study, the researchers show that the production of acetate is also stimulated by low glucose conditions, another condition frequently found in solid tumors.
Acetate, in turn, activates a molecular pathway that ultimately results in the production of several proteins that stimulate the growth and spread of tumors.
“Our study shows that acetate functions in this context as a growth signal for cancer cells, one that links changes in metabolism within cancer cells that occur during tumor growth with activation of a selective stress-signaling pathway. This same signaling pathway is normally protective in healthy individuals. In fact, stimulating this pathway in anemic mice without cancer has a profound effect on restoring red blood cell levels to near-normal or normal levels, and is otherwise very safe” said Dr. Garcia, a member of the Harold C. Simmons Comprehensive Cancer Center.
“The challenge facing us now is to define which patients may benefit from having this pathway stimulated and which patients will benefit from having this pathway inhibited. Preclinical studies of this nature are essential for informing the pharmaceutical and federal health oversight agencies about potential benefits as well as potential harms that may result from use of compounds that affect this key signaling pathway,” said Dr. Garcia.
Other researchers involved in the work include Dr. Robert D. Gerard, Associate Professor of Molecular Biology; Min Xu, Research Scientist; Jason Nagati, Research Assistant; researchers Alok Das and Richard Hogg; and Dr. Rui Chen, former Assistant Professor of Internal Medicine.
The research was supported by funds provided by the Department of Veterans Affairs and the National Institutes of Health.