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Old chemo drug, new pancreatic cancer therapy?

image of Pancreatic ductal adenocarcinoma
Pancreatic ductal adenocarcinoma (red) resists the body’s immune response by surrounding itself with a protective lining that keeps T cells (green) at bay.

The fight against cancer is an arms race, and one of the most effective weapons in clinicians’ arsenals is immunotherapy. Immune checkpoint therapy has become the standard for treating several types of cancer. However, the Nobel Prize-winning strategy is ineffective for most pancreatic ductal adenocarcinoma (PDAC) patients.

“Immune checkpoint therapy is only an option in rare cases of PDAC,” Cold Spring Harbor Laboratory (CSHL) Professor Douglas Fearon says. “It’s only effective for patients with a specific subtype of PDAC—that’s less than 5% of all cases.”

Until recently, it was thought that PDAC didn’t trigger any kind of immune response. In 2023, Fearon and his team confirmed the opposite. Immune cells do go on the attack. But they struggle to infiltrate the deadly tumors, which allows PDAC to avoid destruction. Now, Fearon and former CSHL postdoc Jiayun Li have discovered that a common chemotherapy supplement called folinic acid weakens the cancer’s defenses in mice. They found that folinic acid elevates levels of two anti-cancer immune molecules within PDAC: natural killer T (NKT) cells and type-I interferons. In mice, this leads to a more effective immune response, slower tumor growth, and longer survival. Fearon says:

“We discovered that NKT cells enabled type-I interferon to be produced and, as a consequence, adaptive immune killing and expansion of T cells would occur. T cells respond to tumors, but they typically cannot get in there unless type-I interferon is produced. Folinic acid enhances that response.”

image of Jaiyun Li and Philip Moresco looking at slides in a lab
Former CSHL postdoc Jiayun Li (left) was lead author of the study, co-authored by CSHL Professor and Cancer Center Member Douglas Fearon and Fearon lab member Philip Moresco (right). Li is now a senior research associate at Duke University Medical Center.

PDAC resists immune cells, using a protective shield built from two proteins—CXCR4 and CXCL12. This defensive wall is virtually impenetrable. But when the team treated PDAC tumors with folinic acid, cracks were revealed. The resulting elevated levels of NKT cells and type-I interferons acted like trail markers, highlighting a way past PDAC’s defenses. Cancer-killing immune cells that had been kept outside the wall were able to slip into the tumor and start fighting back.

The Fearon lab now aims to translate its discovery into new therapeutics. They’ve recently partnered with biotech company Autobahn Labs to develop potential drugs targeting CXCR4 and CXCL12. These may one day make immune checkpoint therapy a regular option in the fight against PDAC.

“Translating observations in mice into human therapy has been difficult,” Fearon says. “But if we’re successful, immunotherapy may one day become a viable choice for all patients with PDAC—and every other solid tumor—not just in the rare cases we see today.”

Written by: Nick Wurm, Communications Specialist | wurm@cshl.edu | 516-367-5940


Funding

Lustgarten Foundation, Thompson Family Foundation, Cedar Hill Foundation, Simons Foundation, Mestag Therapeutics, National Institutes of Health, National Cancer Institute

Citation

Li, J., et al., “Intratumoral NKT cell accumulation promotes antitumor immunity in pancreatic cancer”, Proceedings of the National Academy of Sciences, July 8, 2024. DOI: 10.1073/pnas.240391712

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Principal Investigator

Douglas Fearon

Douglas Fearon

Professor
Cancer Center Member
M.D., Johns Hopkins University School of Medicine, 1968

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