News Release

Drugs in development for cancer may also fight brain diseases, including ALS

PARP inhibitors show promise in preventing toxic accumulations of brain disease proteins in Penn research study

Peer-Reviewed Publication

University of Pennsylvania School of Medicine

Under Stress

image: In cells under duress, stress granules (in magenta) form outside of the nucleus (in blue). TDP-43 protein in green (arrow) that cannot bind to PolyADP ribose (PAR) builds up in large clumps distinct from stress granules. view more 

Credit: Leeanne McGurk, University of Pennsylvania; <em>Molecular Cell</em>

PHILADELPHIA - A class of cancer drugs called PARP inhibitors could be useful for treating and preventing brain disorders, including amyotrophic lateral sclerosis (ALS), also called Lou Gehrig's disease, and some forms of frontotemporal degeneration (FTD), by halting the misplacement of specific proteins that affect nerve cells, according to a study published in Molecular Cell by researchers in the the School of Arts and Sciences and the Perelman School of Medicine at the University of Pennsylvania.

The protein TDP-43, when mistakenly outside the nucleus, forms clumps in brain cells that are affected in ALS and FTD. When out-of-place TDP-43 binds to another molecule, PAR, it amasses in cellular structures called stress granules. While this initial accumulation does not cause imminent harm to a cell, after a prolonged period, TDP-43 changes into structures that are observed in brain diseases. Now, a team led by Nancy Bonini, PhD, a professor of Biology, and James Shorter, PhD, a professor of Biochemistry and Biophysics, have found that PARP inhibitors, which stop PAR from being generated, reduced the amount of harmful TDP-43 structures in cells under stress.

Diseases like ALS and FTD-TDP-43 are devastating both for the patient and family and there are limited treatment options. "What excited me about pursuing this pathway was the promise of small molecules that attack the disease process of TDP-43," said lead author Leeanne McGurk, PhD, a research associate in Bonini's lab. "When I tested them on cultured cells, I found they could alleviate the buildup of TDP-43 that mirrors the abnormal protein clumps we see in disease."

In test-tube experiments, the team found that TDP-43 can change from a soluble form to a condensed liquid form by interacting with other TDP-43 molecules and macromolecules like PAR. "The liquid form of TDP-43 is representive of a stress granule and is likely beneficial," Shorter said; however, he noted that if these liquid forms of TDP-43 solidify with time they can be difficult to remove.

This study's promise is that a drug in development as a cancer therapeutic could be used to prevent the formation of harmful TDP-43 clumps in cells. "The PARP inhibitors we tested that antagonized the cytoplasmic accumulation of TDP-43 may one day be optimized as valuable therapeutics for brain diseases," said coauthor Edward Gomes, MS, a research specialist Shorter's lab.

While this work is still being done in the lab, the team's findings provide the next step for neurologists looking for new ways to fight neurodegenerative disorders. "Given the lack of treatment options, we are excited by these experiments that help elucidate molecular events that could lead to new therapeutics," said Bonini

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This research funded by these sources: Ellison Medical Foundation, American Federation for Aging Research, Alzheimer's Association, Life Extension Foundation, ALS Association, Target ALS, Glenn Foundation (NMB), Robert Packard Center for ALS Research at Johns Hopkins, and the National Institute of Health (R01 NS095746-01, R21NS093439, 5R21NS087077-02, R01GM099836, R21NS090205, 5R01NS073660, R35NS097275).

Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $7.8 billion enterprise.

The Perelman School of Medicine has been ranked among the top medical schools in the United States for more than 20 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $405 million awarded in the 2017 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania and Penn Presbyterian Medical Center -- which are recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report -- Chester County Hospital; Lancaster General Health; Penn Medicine Princeton Health; Penn Wissahickon Hospice; and Pennsylvania Hospital - the nation's first hospital, founded in 1751. Additional affiliated inpatient care facilities and services throughout the Philadelphia region include Good Shepherd Penn Partners, a partnership between Good Shepherd Rehabilitation Network and Penn Medicine, and Princeton House Behavioral Health, a leading provider of highly skilled and compassionate behavioral healthcare.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2017, Penn Medicine provided $500 million to benefit our community.


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