Much like using dimmer switches to brighten or darken rooms, biochemists have identified a protein that can be used to slow down or speed up the growth of brain tumors in mice.
Brain and other nervous system cancers are expected to claim 14,320 lives in the United States this year.
The results of the preclinical study led by Dr. Eric Wagner and Dr. Ann-Bin Shyu, in the Department of Biochemistry and Molecular Biology, and Dr. Wei Li, of Baylor College of Medicine, appear in the Advance Online Publication of the journal Nature.
“Our work could lead to the development of a novel therapeutic target that might slow down tumor progression,” said Wagner, assistant professor.
“This link to brain tumors wasn’t previously known,” added Shyu, professor and holder of the Jesse H. Jones Chair in Molecular Biology.
Wagner, Shyu, Li and their colleagues discovered a way to slow tumor growth in a mouse model of brain cancer by altering the process by which genes are converted into proteins.
“Its role in brain tumor progression was first found through big data computational analysis, then followed by animal-based testing. This is an unusual model for biomedical research but is certainly more powerful and may lead to the discovery of more drug targets,” said Li, an associate professor in the Dan L. Duncan Cancer Center and Department of Molecular and Cellular Biology at Baylor.
Appropriately called messenger RNA for short, these molecules take the information inside genes and use it to make body tissues. While it was known that the messenger RNA molecules associated with the cancerous cells were shorter than those with healthy cells, the mechanism by which this occurred was not understood.
The research team discovered that a protein called CFIm25 is critical to keeping messenger RNA long in healthy cells and that its reduction promotes tumor growth. The key research finding in this study was that restoring CFIm25 levels in brain tumors dramatically reduced their growth.
“Understanding how messenger RNA length is regulated will allow researchers to begin to develop new strategies aimed at interfering with the process that causes unusual messenger RNA shortening during the formation of tumors,” Wagner said.
Additional preclinical tests are needed before the strategy can be evaluated in humans.
The work described in the Nature paper by Drs. Wagner and Shyu stems from a high-risk/high-impact Cancer Prevention & Research Institute of Texas (CPRIT) proposal they submitted together and received several years ago.
“Their research is of fundamental biological importance in that it seeks to understand the role of messenger RNA length regulation in gene expression,” said Dr. Rod Kellems, chair of the Department of Biochemistry and Molecular Biology. “Using a sophisticated combination of biochemistry, genetics, and bioinformatics, their research uncovered an important role for a specific protein that is linked to glioblastoma tumor suppression.”
Other UTHealth contributors include postdoctoral fellow Dr. Chioniso Masamha; research associate Todd Albrecht; and neurosurgery associate professor Dr. Min Li, along with a postdoctoral fellow in his lab, Dr. Jingxuan Yang.
“Grade IV astrocytomas (GBM) are the most frequent and malignant form of brain tumor, with a median survival time of only 14.6 months. The mechanisms underlying gliomagenesis remain largely unknown, and limited choices are available for patients with GBM,” said Min Li, director of the Cancer Research Program in the Vivian L. Smith Department of Neurosurgery and a member of the Mischer Neuroscience Institute at Memorial Hermann-Texas Medical Center.
Wagner, Shyu and Min Li are on the faculty of The University of Texas Graduate School of Biomedical Sciences at Houston. Dr. Zheng Xia, a postdoctoral in the laboratory of Wei Li, also contributed to the study.
The study titled “CFIm25 links Alternative Polyadenylation to Glioblastoma Tumour Suppression” received support from the Department of Defense (W81XWH-11-1-0304, W81XWH-12-1-0218, and W81XWH-10-1-0501), National Institutes of Health grants (GM046454, CA167752, CA166274, and HG007538), CPRIT (RP100107 and RP110471-C3), the Houston Endowment, Inc., the Marnie Rose Foundation, and the William and Ella Owens Medical Research Foundation.
-Rob Cahill, Office of Advancement, Media Relations