HMN 2025: How Tumor cells can exploit damaged tissue in the pancreas to create new environments for growth

Pancreatic cancer is an aggressive disease, and unlike many other cancers, survival rates have barely improved. Researchers at Karolinska Institutet, in collaboration with the Department of Pathology at Karolinska University Hospital, have now shown that pancreatic tumor cells not only spread in the connective tissue–rich environment that is a well-known characteristic of pancreatic cancer but also grow into damaged parts of normal pancreatic tissue. There, the cancer can create its own environment.

The study, published in Nature Communications, is based on samples from 108 patients who underwent surgery at Karolinska University Hospital. In almost all cancers, tumor cells were found in the tissue that produces digestive enzymes, but it is damaged when tumor cells grow into it.

“We see that the tumor cells adapt to the environment they find themselves in. In damaged areas of normal pancreatic tissue, they exhibit different characteristics than in the connective tissue-rich part of the tumor,” says Marco Gerling, a researcher at the Department of Clinical Science, Intervention and Technology, Karolinska Institutet, who led the study together with pathologist Carlos Fernández Moro.

May affect treatment response

The researchers also observed that tumor cells in the damaged areas more often had a so-called “classical” tumor profile, while cells in the connective tissue-rich part had a more aggressive profile. The damaged areas contained support cells that express a specific protein, NGFR, which has previously been linked to the healing process of damaged tissue.

“This type of damaged tissue may play a role in how the tumor develops and responds to treatment,” concludes Gerling.

The study was done in collaboration with doctors at Karolinska University Hospital and researchers at Uppsala University, SciLifeLab, and the University of Bergen.

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