- Posted Wednesday January 13, 2016
TGen study published today targets SGEF protein in treating glioblastoma brain tumors
Study funded by Ivy Foundation shows SGEF plays roles in how cancer cells survive and invade brain tissue
PHOENIX, Ariz. - Jan. 13, 2016 - TheTranslational
Genomics Research Institute (TGen) has identified a protein
called SGEF that promotes the survival of glioblastoma tumor cells
and helps the cancer invade brain tissue.
TGen researchers identified SGEF as a target for new brain cancer therapies in a study published today by Molecular Cancer Research, a journal of the American Association for Cancer Research, the world's largest professional organization dedicated to advancing cancer research.
Glioblastoma multiforme, or GBM, is the most common primary tumor of the brain and central nervous system. One of the primary treatments for glioblastoma is surgical removal of the tumor. However, because of the aggressive way glioblastomas invade surrounding brain tissue, it is impossible to remove all parts of the tumors, and the cancer eventually returns and spreads.
This study found that SGEF also plays a role in how glioblastoma tumors develop resistance to treatment. Following surgery, GBM is treated with radiation and the standard-of-care chemotherapy drug called temozolomide (TMZ),
"We need to identify the genetic and cellular-pathway signaling mechanisms that make brain tumors resistant to treatment," said Dr. Nhan Tran, Associate Professor and head of TGen's Central Nervous System Tumor Research Lab. "And the role of SGEF in promoting chemotherapeutic resistance highlights this previously unappreciated protein. Importantly, this also suggests that SGEF could be a new candidate for development of targeted therapeutics," said Dr. Tran, the study's senior author.
This study was funded, in part, by The Ben & Catherine Ivy Foundation.
"Contributing to the progress, TGen studies are helping uncover the mysteries behind glioblastoma," said Catherine (Bracken) Ivy, founder and president of the Arizona-based Ben & Catherine Ivy Foundation. "This research is fundamental to helping patients survive longer and critical to our goal of improving treatments, and eventually finding a cure."
The ability of cancer cells to survive is influenced by the proteins that regulate cellular pathways involved in promoting how cells grow, replicate and spread, as well as whether cells will die when exposed to anti-cancer drugs. Radiation and drug treatment of GBM can lead to DNA damage. This study shows that SGEF promotes cancer cell survival in response to TMZ treatmentbyallowingtumor cells to rapidly repair the damaged DNA that otherwise would lead to cell death.
"Our study shows that SGEF may have an important role in helping cells survive injury - known as the pro-survival cellular signaling response - including injury to common drugs used to treat brain cancer such as TMZ," said Dr. Shannon Fortin Ensign, the study's lead author.
"The roles of invasion and survival are interconnected in the promotion of disease progression," said Dr. Fortin Ensign, a former researcher at TGen who now is a resident in Internal Medicine at Scripps Green Hospital in La Jolla, Calif. "SGEF presents a novel hub in the interrelated axes of tumor cell invasion and survival."
The study, SGEF is Regulated via TWEAK/Fn14/NF-κB Signaling and Promotes Survival by Modulation of the DNA Repair Response to Temozolomide, was published online today by AACR's Molecular Cancer Research.
Founded in 1907, AACR is the world's oldest and largest professional organization dedicated to advancing cancer research and its mission to prevent and cure cancer. AACR membership includes more than 35,000 laboratory, translational and clinical researchers; population scientists; other health care professionals; and cancer advocates in 97 countries.
This study was funded by: the National Institutes of Health under grant number R01 CA130940; by the ARCS Foundation Eller Scholarship and Science Foundation Arizona Fellowship; and by The Ben & Catherine Ivy Foundation.
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About The Ben & Catherine Ivy Foundation
The Ben & Catherine Ivy Foundation, based in Scottsdale, Ariz., was formed in 2005, when Ben Ivy lost his battle with glioblastoma multiforme (GBM). Since then, the Foundation has contributed more than $50 million to research in gliomas within the United States and Canada, with the goal of better diagnostics and treatments that offer long-term survival and a high quality of life for patients with brain tumors. The Ben & Catherine Ivy Foundation is the largest privately funded foundation of its kind in the United States. For more information, visit www.ivyfoundation.org.
The McRae Agency
Translational Genomics Research Institute (TGen) is a Phoenix, Arizona-based non-profit organization dedicated to conducting groundbreaking research with life changing results. TGen is focused on helping patients with neurological disorders, cancer, and diabetes, through cutting edge translational research (the process of rapidly moving research towards patient benefit). TGen physicians and scientists work to unravel the genetic components of both common and rare complex diseases in adults and children. Working with collaborators in the scientific and medical communities literally worldwide, TGen makes a substantial contribution to help our patients through efficiency and effectiveness of the translational process. For more information, visit:www.tgen.org. Follow TGen onFacebook,LinkedInandTwitter @TGen.
TGen Senior Science Writer