Cure Alzheimer's Driving Genes to Therapies

"Our ultimate goal is to develop effective drug therapies at three different points in the pathological cascade of the disease to prevent, inhibit and cure Alzheimer’s."

Building on its enormously successful “Whole Genome Sequencing” Project, which identified nearly 1,000 new genetic mutations in more than 50 different genes, Cure Alzheimer's Fund has announced a new, even more ambitious multi year, $50 million plus program titled “Genes to Therapies” (G2T).

The mission of the Cure Alzheimer's Fund is to fund research with the highest probability of preventing, slowing, or reversing Alzheimer’s disease through venture-based philanthropy.

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Simply put, the new project’s goal is to use the most promising recent genetic discoveries to develop drugs that would stop the disease at three separate stages:

1. For healthy people who don’t yet have Alzheimer’s: to stop Alzheimer’s before it starts by inhibiting the production of the Abeta protein and/or clearing it from the brain after it forms.
2. For those exhibiting symptoms of Alzheimer’s: to stop the process early on by inhibiting the formation of tau tangles and protecting neurons from undue stress.
3. For those whose disease has progressed significantly: to reduce the Abeta and tau-provoked inflammation, slowing down or even stopping the disease process.

“This is indeed a major challenge,” said Research Consortium Chair Dr. Rudy Tanzi, “but I believe we now have the data, the technology and the funding to take it on.”

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The first step, he explained, will be to prioritize approximately 15 genes that fit key several key criteria:

1. They must have a clear impact on Alzheimer’s pathology.
2. They must be “druggable”—connected to known biological systems, producing proteins similar to those already targeted by other drugs.
3. They must impact one of the clear intervention points—Abeta/plaque production, tangle formation or neuroinflammation.

G2T will be aided significantly by the recent “Alzheimer’s-in-a-dish” breakthrough by Tanzi and Dr. Doo Kim at Massachusetts General Hospital.

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Using human brain cells generated from induced pluripotent stem (iPS) cells, Dr. Kim was—for the first time—able to create both the amyloid plaque and neurofibrillary tangle pathology of AD in a Petri dish. This technology will enable much cheaper and faster drug testing.

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“Having learned much about the pathway that leads to disease, together with the genes responsible,” said Tanzi, “we now can proceed to look for chemical compounds that correct the defects. In other words, we can try to fix what is broken.”

To ensure the success of the G2T program, Cure Alzheimer’s Fund is funding a unique research facilitation process—the “infrastructure” for the project.

Unlike most projects, which require six to nine months’ preparation time before any real research begins, our unique approach will save money and, most importantly, time, allowing our researchers to get started right away.

Working as one, our G2T Steering Committee’s ultimate goal is to develop effective drug therapies at three different points in the pathological cascade of the disease to prevent, inhibit and cure Alzheimer’s.

Click here for a quick look at each of the players.


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