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Let鈥檚 get on pancreatic cancer鈥檚 nerves

Microscopic view of neural networks in tissue, highlighted in bright magenta and cyan on a black background.
Stress signals redesign tissues during inflammation and cancer. Left: Normal tissue maintenance. Right: Stress signals 鈥渟witch on鈥 fibroblasts, turning them into myCAFs (purple) that actively recruit nerves (cyan) into the pancreas.

Pancreatic cancer has a lot of nerve. Notoriously tricky to detect, the disease also often resists traditional therapy. So, researchers are urgently looking for new ways to disrupt tumor formation. Though scientists know that the nervous system can help cancer spread, its role in the disease鈥檚 earliest stages remains unclear. 鈥淥ne phenomenon that is known is called perineural invasion,鈥 says Jeremy Nigri, a postdoc in Professor David Tuveson鈥檚 lab at 黑料吃瓜资源 (CSHL). 鈥淭his means cancer cells will migrate within the nerve and use the nerve as a way to metastasize.鈥

Now, Nigri and his colleagues at CSHL have discovered that the nervous system plays an active part in pancreatic cancer development, even before tumors form. Using 3D imaging, they found that tumor-promoting fibroblasts called myCAFs send out signals to attract nerve fibers. The myCAFs and nerve cells then work together within pancreatic lesions to create a favorable environment for cancer to grow. The findings are reported in Cancer Discovery, a journal of the American Association for Cancer Research.

A technique called whole-mount immunofluorescence enabled Tuveson鈥檚 team to take 3D photographs of the lesions and surrounding cells. Where standard 2D images show thin nerve fibers as scattered tiny dots, the 3D images reveal a dense network of nerves snaking through and around the myCAFs and lesions. 鈥淲hen we first saw this picture, I was shocked,鈥 Nigri says. 鈥淚 couldn鈥檛 even imagine the lesion like this. I鈥檇 only ever seen it in 2D.鈥

3D images reveal the highly innervated microenvironment of pre-cancerous pancreatic lesions, seen here as red bubbles. Note the network of nerves in cyan and myCAFs in white.

Nigri and his colleagues ran a series of experiments on mice and human cells that uncovered a vicious cycle between myCAFs and nerves. They found myCAFs give off signals that attract nerve fibers from the sympathetic nervous system, which is responsible for our fight-or-flight response. These nerve fibers release the neurotransmitter norepinephrine, which binds to the fibroblasts and triggers a calcium spike that further activates myCAFs. This spike not only promotes pre-cancerous growth, but also pulls in even more nerve fibers, locking the system into a dangerous self-reinforcing loop.

鈥淚n one experiment, we use a neurotoxin to disable the sympathetic nervous system,鈥 Nigri says. 鈥淲e show reduced fibroblast activation and a nearly 50% reduction in tumor growth.鈥

Because the myCAF-nerve loop happens so early, disrupting this cycle could lead to potential new therapies. The findings suggest that clinically available drugs, including doxazosin, may be effective when combined with standard treatments like chemotherapy or immunotherapy. 鈥淭丑别 next step will be to study this more in detail and try to find a way to block the crosstalk between fibroblasts and nerves,鈥 Nigri says. 鈥淲ith support from groups like the Lustgarten Foundation and Pancreatic Cancer Action Network, we hope to one day help improve patient outcomes.鈥

Written by: Margaret Osborne, Science Writer | [email protected] | 516-367-8455


Funding

National Institutes of Health, Defense Health Agency, Lustgarten Foundation, Thompson Foundation, Pershing Square Foundation, Simons Foundation, CSHL-Northwell Health Affiliation, 黑料吃瓜资源 Association, U.S. Department of Defense, Pancreatic Cancer Action Network, National Cancer Institute, Donaldson Foundation, Northwell Health Cancer Institute

Citation

Nigri, J., et al., 鈥淢yofibroblasts induce neuroplasticity to promote pancreatic inflammation and cancer progression鈥, Cancer Discovery, February 9, 2026. DOI:

Core Facilites

Animal Facility 鈥淭丑别 Animal Shared Resource houses and cares for the animals essential for scientific research. Our staff perform all aspects of animal husbandry, ensure humane care, and assist researchers with highly technical procedures and protocol design and development.鈥 鈥 Animal Facility Director and Attending Veterinarian Rachel Rubino, DVM

鈥淭丑别 Flow Cytometry Shared Resource offers researchers equipment, training, and assistance with cellular analysis for a variety of applications as well as cell sorting. Our staff oversees equipment maintenance and quality control, trains new users on instrument operation, and assists with assay development and data analysis. We also provide tissue culture facilities for sample preparation and cell maintenance during ongoing flow cytometry experiments.鈥 鈥 Director Pamela Moody

image of the microscopy core facility icon 鈥淭丑别 Microscopy Core Facility provides training, consultation, experimental design and technical assistance to investigators at CSHL in widefield, spinning disk laser scanning or point laser scanning confocal fluorescence microscopy, and super-resolution microscopy. In addition, the Microscopy Shared Resource provides customized state-of-the-art optical imaging and quantitative image analysis applications to support a wide range of scientific endeavors.鈥 鈥 Director Erika Wee, Ph.D.

Neuroimaging and Behavior icon 鈥淭丑别 Neuro-Imaging and Behavior Core Facility helps bridge the gap between recent innovations in optical or ultrasound imaging and the state-of-the-art rodent behavioral and neural circuit models and technologies at CSHL. We bring together state-of-the-art imaging and photo-stimulation solutions for neuroscience research in rodent models.鈥 鈥 Director Sanjeev Kaushalya

image of single-cell biology icon 鈥淭丑别 Single Cell Genomics Core Facility brings cutting-edge single-cell technologies to collaborators both inside and outside of the Laboratory. We currently specialize in single-cell transcriptomics and offer assistance in a variety of gene expression workflows, including the latest in spatial gene expression profiling technologies.鈥 鈥 Director Jon Preall, Ph.D.

Animal Tissue Imaging 鈥淭丑别 Tissue Imaging Shared Resource provides a spectrum of on-demand and researcher-tailored histopathological services, including tissue sampling, processing, embedding, and sectioning, as well as H&E, special, and immunohistochemistry staining. We not only support laser-capture microdissection and whole-slide scanning, but also offer histopathology consultation and instrument training.鈥 鈥 Manager Kristin Milicich

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Principal Investigator

David Tuveson

David Tuveson

Professor
Roy J. Zuckerberg Professor of Cancer Research
Cancer Center Director
M.D., Ph.D., Johns Hopkins University, 1994

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