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GEN News Highlights : Apr 19, 2013
Stem Cell Screen Reveals Promising Target for ALS
Researchers say they found a compound more effective in protecting the neurons killed in amyotrophic lateral sclerosis (ALS; Lou Gehrig’s disease) than two drugs that failed in clinical trials after hundreds of millions of dollars had been invested in them. The team, from Harvard Stem Cell Institute (HSCI), used a new stem-cell based drug screening technology that they say has the potential to reinvent and greatly reduce the cost of new pharmaceutical development. They say their technique successfully predicted that the two drugs that eventually failed in the third and final stage of human testing would, in fact, fail.
“It’s a deep, dark secret of drug discovery that very few drugs have been tested on human-diseased cells before being tested in a live person,” says Lee Rubin, Ph.D., who developed the new stem cell screening technique. Dr. Rubin is a member of HSCI’s executive committee, a professor in Harvard’s department of stem cell and regenerative biology, and head of HSCI’s program in translational medicine. “We were interested in the notion that we can use stem cells to correct that situation.”
Dr. Rubin’s model is built on an earlier proof-of-concept developed by HSCI principal faculty member Kevin Eggan, who demonstrated that it was possible to move a neuron-based disease into a laboratory dish using stem cells carrying the genes of patients with the disease. In his study, Dr. Rubin lays out how he and his colleagues applied their new method of stem cell-based drug discovery to ALS. The disease is associated with the progressive death of motor neurons. As cells die, people with ALS experience weakness in their limbs followed by rapid paralysis and respiratory failure. Ten percent of cases are genetically predisposed, but for most patients there is no known trigger.
Dr. Rubin’s lab began by first studying the disease in mice, growing billions of motor neurons from mouse embryonic stem cells, half normal and half with a genetic mutation known to cause ALS. Investigators starved the cells of nutrients and then screened 5,000 drug-like molecules to find any that would keep the motor neurons alive.
Several hits were identified, but the molecule that best prolonged the life of both normal and ALS motor neurons was kenpaullone, previously known for blocking the action of the enzyme GSK-3, which switches on and off several cellular processes including cell growth and death.
“Shockingly, this molecule keeps cells alive better than the standard culture medium that everybody keeps motor neurons in,” Dr. Rubin said.
Kenpaullone proved effective in several follow-up experiments that put mouse motor neurons in situations of certain death. Neuron survival increased in the presence of the molecule whether the cells were programmed to die or placed in a toxic environment.
Dr. Rubin’s lab then discovered that kenpaullone’s potency comes from its ability to also inhibit HGK, an enzyme that sets off a chain of reactions that leads to motor neuron death. This enzyme was not previously known to be important in motor neurons or associated with ALS, marking the discovery of a new drug target for the disease.
To find out if kenpaullone works in diseased human cells, Dr. Rubin’s lab exposed patient motor neurons and motor neurons grown from human embryonic stem cells to the molecule, as well as two drugs—olesoxime and dexpramipexole—that did well in mice but failed in Phase III clinical trials for ALS. Once again, kenpaullone increased the rate of neuron survival, while one drug saw little response, and the other drug failed to keep any cells alive.
Before kenpaullone could be used as a drug, explains Dr. Rubin, it would need a substantial molecular makeover to make it better able to target cells and find its way into the spinal cord so it can access motor neurons.
“This is kind of a proof of principle on the do-ability of the whole thing,” he said. “I think it’s possible to use this method to discover new drug targets and to prevalidate compounds on real human disease cells before putting them in the clinic.”
In the meantime, Dr. Rubin’s next steps will be to continue searching for better drug-like compounds that can inhibit HGK and thus enhance motor neuron survival. He believes that the new information that comes out of this research will be useful to academia and the pharmaceutical industry.
“I think that stem-cell screens will discover new compounds that have never been discovered before by other methods,”Dr. Rubin says. “I’m excited to think that someday one of them might actually be good enough to go into the clinic.”
The study was published yesterday in the journal Cell Stem Cell, in a paper titled “A Small Molecule Screen in Stem-Cell-Derived Motor Neurons Identifies a Kinase Inhibitor as a Candidate Therapeutic for ALS”.
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