News &
Publications

Contacts

Lisa Bailey
Interim Director of Communications
Director of Social Networking
215-214-3954
215-872-5846 (cell phone)
Lisa.Bailey@fccc.edu

Diana Quattrone
Director of Media Relations
215-728-7784
215-815-7828 (cell phone)
Diana.Quattrone@fccc.edu

Communications Staff

 

News

Fox Chase Researchers Identify New Mechanism Used by Cells to Reverse Silenced Genes

Results suggest novel approach to developing targeted cancer therapies

PHILADELPHIA (June 30, 2011) – Scientists at Fox Chase Cancer Center have discovered a new mechanism used by cells in the body to turn on silenced genes. This process is critical in preventing the development of cancer—suggesting the possibility of new therapies that might target the specific changes underlying the disease. The findings will be published online in the journal Cell on June 30, 2011.

The process investigated by Alfonso Bellacosa, MD, PhD, Associate Professor at Fox Chase, and his colleagues, is called methylation, in which the cell chemically tags genes to turn them off. More specifically, the cell silences a gene by adding a chemical compound known as a methyl group; without that methyl group, the gene remains active.

It's a process of great interest to scientists, Bellacosa explains, because methylation is a key part of normal gene regulation – but, when it silences the genes that normally suppress tumors, it results in cancer. Indeed, some cancer drugs work by demethylating—meaning, removing methyl groups from DNA. But those drugs will demethylate DNA non-specifically, he says, causing side effects and other problems.

Now, Bellacosa and his team present the first direct evidence that demethylation can be, in fact, an active process, controlled by a specific protein – along with clues about how to act on it in a targeted way.

The researchers found that one protein called thymine DNA glycosylase or TDG—known to help repair DNA—is also responsible for removing methyl groups from DNA. Studies with mice that lacked TDG activity indicated the gene was needed for survival. Looking closer at the mouse embryos that didn't survive, they saw that the methylation was all awry – genes that would normally be demethylated weren't, and remained silenced.

TDG needs a second protein to demethylate DNA, says Bellacosa - so future therapies might be devised to direct this machinery to turn on specific anti-cancer genes, for instance. "Since we now know there are proteins that actively affect demethylation, then we can imagine a new type of cancer therapy that demethylates specific genes. We would have a more precise and more targeted type of therapy."

What's also exciting, explains Bellacosa, is the discovery that the cell uses tools that normally repair DNA for a very different purpose: reversal of gene silencing by demethylation. "It's a totally new concept – that DNA repair has this additional new function."

Beside cancer, this knowledge may also be applied to other diseases with alteration of methylation. He cautions, however, that scientists still have not figured out how to target therapy to specific genes, so any benefits to this discovery are years away. "This is a very fundamental study that gets at the process by which genes are turned on or turned off," he says. "We may be several years away from taking full advantage of this new knowledge. But we will get there."

Co-authors on the study include Salvatore Cortellino, Jinfei Xu, Mara Sannai, Robert Moore, Elena Caretti, Antonio Cigliano, Madeleine Le Coz, Karthik Devarajan, Maria Rosaria Bassi, Catherine Renner, and Andres J. Klein-Szanto from Fox Chase Cancer Center in Philadelphia; Andy Wessels from the Medical University of South Carolina in Charleston; Dianne Soprano from Temple University School of Medicine in Philadelphia; Lara K. Abramowitz, Marisa S. Bartolomei from University of Pennsylvania School of Medicine in Philadelphia; Florian Rambow, Christophe Alberti, and Lionel Larue from Curie Institute in France; Tiziana Bruno and Maurizio Fanciulli from Regina Elena Cancer Center in Rome; Yoshihiro Matsumoto from East Stroudsburg University in East Stroudsburg; and Dominique Kobi and Irwin Davidson from Institut de Génétique et de Biologie Moléculaire et Cellulaire in France.

The study was supported by grants from the National Institutes of Health (NIH).


Fox Chase Cancer Center, part of the Temple University Health System, is one of the leading cancer research and treatment centers in the United States. Founded in 1904 in Philadelphia as one of the nation’s first cancer hospitals, Fox Chase was also among the first institutions to be designated a National Cancer Institute Comprehensive Cancer Center in 1974. Fox Chase researchers have won the highest awards in their fields, including two Nobel Prizes. Fox Chase physicians are also routinely recognized in national rankings, and the Center’s nursing program has received the Magnet recognition for excellence four consecutive times. Today, Fox Chase conducts a broad array of nationally competitive basic, translational, and clinical research, with special programs in cancer prevention, detection, survivorship, and community outreach.  For more information, call 1-888-FOX CHASE or (1-888-369-2427).

Media inquiries only, please contact Diana Quattrone at 215-728-7784.

More 2011 News Releases »