Pancreatic cancer cells (nuclei in blue) are shown growing as a sphere encased in membranes (red).
Newswise — Pancreatic cancer is the third deadliest cancer in the United States, after lung and colorectal, though far less common. It is also among the hardest to effectively treat, with pancreatic cancer stem cells quickly developing resistance to conventional and targeted treatments, such as chemotherapy and emerging immunotherapies. As a result, the 5-year survival rate for people diagnosed with pancreatic cancer is just 10%.
In a new paper, published January 18, 2023 in Nature Communications, an international team of scientists, led by researchers at University of California San Diego School of Medicine and the Sanford Consortium for Regenerative Medicine, reveal another way in which the most-resistant pancreatic cancer cells defy treatment by leveraging a member of a group of proteins that ordinarily might suppress tumors to instead help cancer cells evade therapy and grow more quickly.
Previous research has shown that pancreatic cancer treatment resistance is caused by differing responses to conventional agents, fueled by the heterogeneity (diversity) of tumor cells — and in particular, stem cell characteristics that encourage therapy resistance.
In the new study, senior author Tannishtha Reya, PhD, formerly a professor of Pharmacology and Medicine and director of the Division of Cancer Biology at UC San Diego School of Medicine, and colleagues investigated how shifting epigenomics (the multitude of proteins that tell the genome what to do) rather than genomic changes (specific to the genes themselves) might be driving resistance.
“Pancreatic cancer stem cells, which are aggressive cancer cells that can resist conventional therapies and drive tumor relapse, rely upon epigenetic regulation to protect themselves and promote survival and growth,” said Reya, now a professor of Physiology and Cellular Biophysics at Columbia University and associate director of translational research at the Herbert Irving Comprehensive Cancer Center.
“We wanted to identify the underlying tools and mechanisms that cancer stem cells use to better understand treatment resistance — and perhaps how they might be circumvented.”
Reya and colleagues zeroed in on SMARCD3, a member of the SWI/SNF family of proteins that regulate chromatin, a mixture of DNA and proteins that form chromosomes and are required for stem cell function in development.
But while SWI-SNF subunits often act as tumor suppressors, the researchers found that SMARCD3 was amplified in cancer, notably abundant in pancreatic cancer stem cells and upregulated or increased in the human disease.
And when researchers deleted SMARCD3 in models of pancreatic cancer, the loss of the protein reduced the growth of tumors and improved survival, especially in the context of chemotherapy.
“Importantly, we found that SMARCD3 helps control lipid and fatty acid metabolism, which are associated with therapy resistance and poor prognosis in cancer,” said Reya.
“Our data suggest that therapy resistant pancreatic cancer cells depend upon SMARCD3 to help ensure a metabolic landscape in which they can avoid anti-cancer treatments and grow aggressively. That makes SMARCD3 an exciting new target for potential therapies.”
Co-authors include: L. Paige Ferguson, Matthew L. McDermott, Mari Nakamura, Kendall Chambers, Nirakar Rajbhandari and Michael Hamilton, all at UC San Diego and Sanford Consortium for Regenerative Medicine; Jovylyn Gatchalian, Nikki K. Lytle and Diana C. Hargreaves, Salk Institute for Biological Studies; Sara Brin Rosenthal and Vera Vavinskaya, UC San Diego; Sonia Albini, Université Paris-Saclay, Univ Evry, Inserm, Genethon, Integrare; Martin Wartenberg, Inti Zlobec and José A. Galván, Eva Karamitopoulou, all at University of Bern, Switzerland; Alexis Wascher and Andrew M. Lowy, UC San Diego and Moores Cancer Center; Christian M. Schürch, University Hospital and Comprehensive Cancer Center Tübingen, Germany; Pier Lorenzo Puri, Sanford Burnham Prebys Medical Discovery Institute; and Benoit G. Bruneau, UC San Francisco.
Funding for this research came, in part, from the National Institutes of Health (grants T32 GM007752, T32 GM007752, T32 HL086344, T32 CA009370 R01 CA186043 and R35 CA197699 ), Ruth L. Kirschstein National Research Service Awards (F31 CA247489 and F32 GM128377), the Tobacco-Related Disease Research Program (grants T29FT0280 and T32FT5133), an AACR-Bayer START Award (20-40-44-NAKA), an American Cancer Society Scholar Award, the Pew-Stewart Scholars Program for Cancer Research and a SU2C–CRUK–Lustgarten Foundation Pancreatic Cancer Dream Team Research Grant (SU2C-AACR-DT-20-16).
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