Tara Mastren, center, and Aidan Bender, right. Mastren鈥檚 lab at the University of Utah has published new research that shows promise for developing targeted alpha therapies for Alzheimer鈥檚. Also pictured is former graduate student Connor Holiski.
News — Alzheimer’s disease, a debilitating brain disorder with limited treatment options, has long challenged researchers. Specifically, researchers have struggled with slowing the buildup of , harmful clumps of proteins that exacerbate the disease by damaging brain cells and causing memory loss.
Led by the John and Marcia Price , University of Utah researchers have developed a groundbreaking approach to tackle these plaques and possibly slow this devastating neurodegenerative disease.
Inspired by targeted cancer treatment methods, their technique utilizes a form of radiation known as alpha particles to break down chemical bonds in amyloid beta plaques. Targeted Alpha Therapy (TAT) delivers these particles directly to the harmful plaques on the brain while aiming to minimize damage to healthy tissues.
, a former graduate student in the college’s , spearheaded this in the Journal of Nuclear Medicine, the premier journal in the field. Co-authors included researchers from the Utah's departments of Radiology and Chemistry.
“Aidan excelled in research and developed many skills and techniques needed to tackle this study,” said the study’s senior author , an assistant professor of civil & environmental engineering whose focuses on developing . “The research from his publication is the first step in determining if this treatment method is feasible and has allowed us to move into testing in vivo models.”
New hope for Alzheimer’s patients
is a leading cause of dementia in the United States, resulting in more than $200 billion in medical expenses a year. The number of cases is expected to double by 2050, but the disorder’s impact could be lessened if treatments can be developed to slow its progress.
The Utah researchers turned to theoretical nuclear medicine in search of answers.
Under Mastren’s supervision, Bender’s team started by developing a chemical compound, called BiBPy, that can latch onto to the harmful amyloid beta plaques.
They attached a small amount of a radioactive isotope, bismuth-213, enabling the compound to emit alpha particles. This new compound, [213Bi]-BiBPy, was applied to the brain tissue of mice that were genetically modified to develop amyloid plaques similar to those in Alzheimer’s patients.
The compound, when combined with bismuth-213, demonstrated properties that made it effective at binding to the mice’s amyloid plaques.
Measured using two types of tests for the presence of amyloid beta, the treated brain tissues showed a significant reduction in amyloid beta concentration. that the compound may be effectively applied as a potential TAT treatment for Alzheimer’s and other neurodegenerative diseases, paving the way for further tests in live animals and eventually in humans.
Since earning his doctorate, Bender has joined the at Huntsman Cancer Institute where he works on radiopharmaceutical development for cancer imaging and therapy. By harnessing cyclotron-produced therapeutic radionuclides, auger electron therapy, and PET radiometals, his research may lead to new tools for detecting, diagnosing and treating cancer.
This research was supported the university’s , which aims to bring together researchers from health sciences and the main campus to broaden the societal impact of the university’s research. Engineering faculty worked in collaboration with , an associate professor of chemistry, and his graduate student Emily Kirkeby, and and of the Department of Radiology.
The study, titled “Development of a Bismuth-213 Labeled Pyridyl Benzofuran for Targeted α-Therapy of Amyloid-β Aggregates,” was published July 25 online by the . Funding came from the National Cancer Institute, University of Utah and the NRC Graduate Research Fellowship program.
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