The team presented their findings about the agent, CM101 (also known as BK40143), in an oral presentation at the annual meeting of the Society for Neuroscience in Chicago on Oct. 22.
CM101 works by turning on a neuron’s “garbage disposal” system that is designed to eliminate unwanted and toxic proteins, such as tau and amyloid-beta 42, among other compounds, often found in Alzheimer’s disease, and alpha-synuclein, often found in Parkinson’s disease.
“A very low dose of CM101 flips on the garbage disposal in brain neurons for a few hours a day, just enough to provide a little feast on the neurotoxic proteins in the cells. Over time, this buildup in neurons starts to clear away,” says Georgetown Neurology Associate Professor Charbel Moussa, MBBS, PhD, the senior author of the study and director of the GUMC Translational Neurotherapeutics Program.
This work is a continuation of Moussa’s research into how agents known as tyrosine kinase inhibitors can produce this reaction and potentially halt neurodegenerative diseases. His work has led to clinical trials with two repurposed cancer drugs that are tyrosine kinase inhibitors — nilotinib and bosutinib.
These two drugs are given in doses that are up to 10 times higher to treat leukemia and other blood cancers than what is needed to trigger the clean out of protein buildup in neurons.
“The idea with these frequent high doses is that controlling cell division or proliferation while keeping the garbage disposal working overtime will incinerate cells that are rapidly dividing. These cancer cells will cannibalize themselves,” says Alan Fowler, the study’s first author and a PhD candidate in Moussa’s lab.
The new advance with CM101 reflects research in the Moussa lab that has teased apart the different pathways affected by different tyrosine kinase (TK) inhibitors.
TK enzymes are found in most cell types and have many functions, including cell signaling, growth and division.
The researchers discovered that nilotinib and bosutinib inhibit a number of different TKs, including Abelson (Abl) and Discoidin Domain Receptors 1 and 2 (DDR). However, more in-depth tests show that DDRs may be the master keys to switching on the garbage disposal in brain cells affected by neurodegeneration, Fowler explains.
The new compound, CM101, designed and synthesized in collaboration with chemistry professor Christian Wolf and his team at Georgetown’s Medicinal Chemistry Shared Resource Center, focuses specifically on inhibiting DDR1 and 2.
“We are repurposing TK inhibitor drugs toward neurodegenerative disorders — the vast majority of which feature toxic buildup in brain cells,” Moussa says. “Our studies suggest this strategy works in neurons that are diseased but remain vital enough to be reprogrammed.”
Both nilotinib and bosutinib are being studied in clinical trials for people with neurodegenerative diseases.
“This agent has undergone extensive testing in several animal models of neurodegeneration, and it represents a good candidate that should be investigated in first-in-human trials. We have so far shown that this agent has a superior efficacy to clear neurotoxic proteins in animals compared to similar agents, and we identified DDRs as a preferential and optimal drug target. The next step is to investigate drug toxicity in order to obtain regulatory permission for human application,” Moussa added.
In addition to Fowler and Moussa, authors include Michaeline Hebron, MS, Alexander A. Missner, Jonathan Greenzaid, Xiaoguang Liu, MD, PhD, Kaluvu Balaraman, PhD and Christian Wolf, PhD, all of Georgetown University.
This work was funded by the Laboratory for Dementia and Parkinsonism. Georgetown has filed a patent application related to use of certain DDR inhibitors for the treatment of neurodegenerative diseases. Moussa is the named inventor of the intellectual property protected. The other authors report no potential financial interest.
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