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Cancer
Cancer
We are rapidly demystifying cancers, exposing the molecular mechanisms underlying tumors and leading the search for the next generation of targeted cancer therapies. We see a future where every cancer and every patient has a cure.

Cancer

09/2021

The Salk Institute and Sanford Burnham Prebys license ULK1/2 inhibitors to Endeavor BioMedicines for treatment of cancer

In 2015, Salk Professor Reuben Shaw and Professor Nicholas Cosford at Sanford Burnham Prebys (SBP) demonstrated that by chemically blocking the ULK1/2 protein, they could shut down the cellular recycling pathway known as autophagy that some cancer cells use to stay alive. The researchers found small molecule compounds that effectively blocked ULK1/2 and killed cancer cells, including human and mouse lung cancer cells and human pancreatic cancer cells. Now, Salk, along with SBP, has signed an exclusive licensing agreement with Endeavor BioMedicines for an intellectual property portfolio relating to cancer therapeutics and diagnostics that target ULK1/2. Endeavor plans to complete studies and advance the program into the clinic, initially in colorectal and lung cancers, in the next 18 months.

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10/2021

Salk team launches phase 1 clinical trial for Alzheimer’s therapy

In another recent advancement, the investigational Alzheimer’s drug CMS121, developed and studied at Salk over the last 15 years, has now moved into a phase 1 clinical trial to evaluate its safety in humans. Salk Research Professor Pamela Maher and Bill Raschke of Virogenics, Inc., received $4.5 million over two years from the National Institute of Aging to support the trial and expect the first doses to be administered to healthy volunteers in early 2022. In mice, CMS121 reverses signs of aging in the brain and prevents the memory loss associated with Alzheimer’s disease.

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Nature COMM
10/2021

Salk scientists reveal cancer’s most common gene mutations

Genetic mutations play a fundamental role in the development and growth of cancers. However, while many studies have identified the mutations involved in certain cancers, like breast cancer, no one had ever managed to combine the data in a way that could reveal which mutations are most common in the entire cancer patient population. Now, Assistant Professor Edward Stites and his team of computational scientists have combined gene mutation information with cancer prevalence data to reveal the genetic basis of cancer in patients across the United States. The findings could help guide genetic research to develop more effective treatments than presently available.

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