Pancreatic cancer is the third leading cause of cancer-related mortality in the United States, accounting for more than 47,000 deaths annually. Only one in 10 people diagnosed with this particularly aggressive disease live beyond five years, and most therapies -- including conventional chemotherapies, targeted therapies and immunotherapies -- are largely unsuccessful in treating it, doctors say.
"Pancreatic cancer is one of the most challenging cancers to treat,'' said Dr. Caius Radu, a professor of molecular and medical pharmacology at the David Geffen School of Medicine at UCLA. "The lack of effective treatments suggests there is an inadequate understanding of the biologic complexity of the disease and the mechanisms behind its resistance to therapies that work in treating other types of cancers.''
The two grant-supported projects, which will be co-led by Radu and Dr. Timothy Donahue, a professor of surgery and chief of surgical oncology at the Geffen School of Medicine, aim to untangle those complexities and to identify potential new immunotherapeutic approaches.
The first grant project will focus on mutations to the KRAS gene, which are implicated in nearly all pancreatic cancer cases. Mutated KRAS genes drive tumor growth in the pancreas in much the same way mutations to BRCA genes drive the development of breast cancer.
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"Immunotherapy has revolutionized the way we treat a number of malignancies, but to date, its impact in pancreatic cancer has been disappointing,'' said Donahue, who is also the surgical director of the UCLA Agi Hirshberg Center for Pancreatic Diseases. "Conventional immune checkpoint inhibitors approved for use in melanoma, lung cancer and other solid tumors show little or no benefit for the vast majority of pancreatic cancer patients, indicating that additional priming of the immune system will be absolutely necessary to overcome the intrinsic resistance of pancreatic tumors to immunotherapy.''
The second project will focus on interferon signaling in pancreatic cancer. The team will seek to identify vulnerabilities in tumor cells' interferon signaling process that can be leveraged for effective therapeutic strategies.
The researchers have already identified that interferon signaling is upregulated in a subset of human pancreatic cancer cells and functions to deplete nucleotides, which are essential for DNA replication and repair.
They will continue to examine the mechanisms these tumor cells have in place to counterbalance the nucleotide-depleting and potentially deleterious effects of interferon signaling and will explore the potential therapeutic benefits of inhibiting the signaling process.