BGU scientists discover genetic link between aging brain and cancers

Studying cancer teaches us about aging and vice versa," said Dr. Rotblat.

Ben-Gurion University of the Negev. (photo credit: ISRAEL'S FOREIGN AFFAIRS MINISTRY)
Ben-Gurion University of the Negev.
(photo credit: ISRAEL'S FOREIGN AFFAIRS MINISTRY)

Researchers from Ben-Gurion University (BGU) have identified a gene responsible for activating glioblastoma, a type of brain cancer, which is also partly responsible for aging in our brain.

The study, led by Dr. Barak Rotblat of BGU's Department of Life Sciences in the Faculty of Natural Sciences and of the National Institute for Biotechnology in the Negev (NIBN), was published in the peer-reviewed journal Aging late last week.

The same genes that make glioblastoma resistant to chemotherapy are activated in an aging brain, according to the research. And these genes were unknown before the study. "Studying cancer teaches us about aging and vice versa," Rotblat said.

Rotblat's research has focused on a new class of genes coding for long noncoding RNA. Indeed, gene products are usually RNA that code for proteins, but, while there are 20,000 “classic” protein-coding genes, we now know that there are at least 20,000 genes whose products are long noncoding RNA.

“For the past few years, we have been studying one of these genes, TP73-AS1, and found that it is highly active in both pediatric (medulloblastoma) and adult (glioblastoma) brain cancers," explained Rotblat. "Importantly, not only is this gene highly active in brain cancer, but it also contributes to the aggressiveness of the disease. In glioblastoma, high levels of TP73-AS1 in tumor cells provide protection against chemotherapy.”

Using computational and cell biology techniques, such as CRISPR, the Rotblat lab identified a protein increasing TP73-AS1 gene activity in response to chemotherapy and realized that this protein, known as YY1, is also known to activate many genes in the aging brain. Interestingly, aging and glioblastoma are also known to be linked, because glioblastoma is more aggressive in older people.

“Once we found that YY1 increases the activity of TP73-AS1, we asked if, like YY1, TP73-AS1 is also active in the aging brain and found that this is indeed the case. Now, we are excited by the prospect that by studying TP73-AS1 and the molecular pathways it interacts with, we can learn about cancer and aging in the brain,” he says about directions for future studies.

The research was supported by the Israel Science Foundation, the Israeli Cancer Association, NIBN, the David and Inez Myers foundation and the Science and Technology Ministry.