A double edged sword, gene variants may promote overall health while increasing risk of gliomas.
New genomic research led by UC San Francisco scientists reveals that two common gene variants that lead to longer telomeres, the caps on chromosome ends thought by many scientists to confer health by protecting cells from aging, also significantly increase the risk of developing the deadly brain cancers known as gliomas.
The genetic variants, in two telomere-related genes known as TERT and TERC, are respectively carried by 51 percent and 72 percent of the general population. Because it is somewhat unusual for such risk-conferring variants to be carried by a majority of people, the researchers propose that in these carriers the overall cellular robustness afforded by longer telomeres trumps the increased risk of high-grade gliomas, which are invariably fatal but relatively rare cancers.
The research was published online in Nature Genetics on June 8, 2014.
“There are clearly high barriers to developing gliomas, perhaps because the brain has special protection,” said Margaret Wrensch, MPH, PhD, the Stanley D. Lewis and Virginia S. Lewis Endowed Chair in Brain Tumor Research at UCSF and senior author of the new study. “It’s not uncommon for people diagnosed with glioma to comment, ‘I’ve never been sick in my life.’”
In a possible example of this genetic balancing act between risks and benefits of telomere length, in one dataset employed in the current study—a massive genomic analysis of telomere length in nearly 40,000 individuals conducted at the University of Leicester in the United Kingdom—shorter telomeres were associated with a significantly increased risk of cardiovascular disease.
“Though longer telomeres might be good for you as a whole person, reducing many health risks and slowing aging, they might also cause some cells to live longer than they’re supposed to, which is one of the hallmarks of cancer,” said lead author Kyle M. Walsh, PhD, assistant professor of neurological surgery and a member of the Program in Cancer Genetics at UCSF’s Helen Diller Family Comprehensive Cancer Center.
In the first phase of the new study, researchers at UCSF and The Mayo Clinic College of Medicine analyzed genome-wide data from 1,644 glioma patients and 7,736 healthy control individuals, including some who took part in The Cancer Genome Atlas project sponsored by the National Cancer Institute and National Human Genome Research Institute. This work confirmed a link between TERT and gliomas that had been made in previous UCSF research, and also identified TERC as a glioma risk factor for the first time.
Since both genes have known roles in regulating the action of telomerase, the enzyme that maintains telomere length, the research team combed the University of Leicester data, and they found that the same TERT and TERC variants associated with glioma risk were also associated with greater telomere length.
UCSF’s Elizabeth Blackburn, PhD, shared the 2009 Nobel Prize in Physiology or Medicine for her pioneering work on telomeres and telomerase, an area of research she began in the mid-1970s. In the ensuing decades, untangling the relationships between telomere length and disease has proved to be complex.
In much research, longer telomeres have been considered a sign of health—for example, Blackburn and others have shown that individuals exposed to chronic stressful experiences have shortened telomeres. But because cancer cells promote their own longevity by maintaining telomere length, drug companies have searched for drugs to specifically target and block telomerase in tumors in the hopes that cancer cells will accumulate genetic damage and die.
Walsh said the relevance of the new research should extend beyond gliomas, since TERT variants have also been implicated in lung, prostate, testicular and breast cancers, and TERC variants in leukemia, colon cancer and multiple myeloma. Variants in both TERT and TERC have been found to increase risk of idiopathic pulmonary fibrosis, a progressive disease of the lungs.
In some of these cases, the disease-associated variants promote longer telomeres, and in others shorter telomeres, suggesting that “both longer and shorter telomere length may be pathogenic, depending on the disease under consideration,” the authors write.
Notes about this neurology and brain cancer research
In addition to the Mayo Clinic and Leicester University teams, Wrensch and Walsh were joined by colleagues from University Medical Center Groningen in Germany. Other UCSF authors include Ivan V. Smirnov, PhD; Terri Rice, MPH; Helen M. Hansen; Annette M. Molinaro, PhD; Lucie S. McCoy, MPH; Paige M. Bracci, PhD, MPH; Belinda S. Cabriga; Melike Pekmezci, MD; Shichun Zheng, MD; Joseph L. Wiemels, PhD; Tarik Tihan, MD, PhD; Mitchel S. Berger, MD; Susan M. Chang, MD; Michael D. Prados, MD; and John K. Wiencke, PhD. Alexander R. Pico, PhD, of the Gladstone Institutes also took part in the research, as did members of the ENGAGE Consortium Telomere Group.
Research conducted at UCSF was supported by the National Institutes of Health; the National Brain Tumor Foundation; the UCSF Lewis Chair in Brain Tumor Research; the UCSF Robert Magnin Newman chair in Neuro-Oncology; and by donations from families and friends of John Berardi, Helen Glaser, Elvera Olsen, Raymond E. Cooper and William Martinusen.
Contact: Pete Farley – UCSF Source:UCSF press release Image Source: The image is credited to Nevit Dilmen and is licensed Creative Commons Attribution Share Alike 3.0 Unported Original Research:Abstract for “Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk” by Kyle M Walsh, Veryan Codd, Ivan V Smirnov, Terri Rice, Paul A Decker, Helen M Hansen, Thomas Kollmeyer, Matthew L Kosel, Annette M Molinaro, Lucie S McCoy, Paige M Bracci, Belinda S Cabriga, Melike Pekmezci, Shichun Zheng, Joseph L Wiemels, Alexander R Pico, Tarik Tihan, Mitchell S Berger, Susan M Chang, Michael D Prados, Daniel H Lachance, Brian Patrick O’Neill, Hugues Sicotte, Jeanette E Eckel-Passow, Pim van der Harst, John K Wiencke, Nilesh J Samani, Robert B Jenkins and Margaret R Wrensch in Nature Genetics. Published online June 8 2014 doi:10.1038/ng.3004