Interaction with stromal cells influences tumor growth, metastasis in pancreatic cancer

A study from researchers at the Massachusetts General Hospital (MGH) Cancer Center has demonstrated how the response to pancreatic cancer cells of normal tissue – called the stroma – within tumors can influence the ability of individual cancer cells to proliferate and metastasize. Their report, which details how differences in the relative amounts of tumor cells and stromal cells alter patterns of gene expression within individual tumor cells, is being published in Cell and may lead to improved therapies for this difficult-to-treat cancer.

“Our finding that pancreatic cancer cells can behave differently based on the types of cells that are around them may explain why some cells respond to chemotherapy and radiation and some do not,” says David Ting, MD, of the Tucker Gosnell Center for Gastrointestinal Malignancies in the MGH Cancer Center, co-senior author of the report. “We also identified a unique cell type that has the ability to replicate and to move at the same time, activates both the MAPK and STAT3 signaling pathways and is killed by combined use of MAPK and STAT3 inhibitors, suggesting a potential therapeutic strategy.”

The stroma of pancreatic tumors largely consists of connective tissue cells called cancer-associated fibroblasts (CAFs), along with immune cells and endothelial cells. While some studies have suggested that pancreatic CAFs contribute to the growth and spread of cancer, others have found that reducing CAFs led to more aggressive tumor behavior. These findings, along with the variability of stromal content within pancreatic tumors, suggested that interactions between CAFs and tumor cells are complex.

Recent studies by the MGH team found significant differences in gene expression between pancreatic cancer cells in the primary tumor and those circulating in the bloodstream, with some expressing signatures indicating proliferative features and others more metastatic potential. Subpopulations of cancers cells at the interface between tumor and stroma also expressed these differing genetic signatures, suggesting that they might be influenced by CAFs in the stroma.

The team’s current experiments revealed that:

• Culturing pancreatic tumor cells (PDACs) with CAFs led to changes in gene expression within cancer cells based on the relative proportions of the two types of cells within the culture. These differences allowed PDACs to be grouped into classes expressing either proliferative or metastatic/invasive signatures, and a subpopulation of “double-positive” cells simultaneously expressing both signatures was primarily seen in cultures with the highest proportion of CAFs.
• Tumors with different PDAC:CAF ratios implanted into immunodeficient mice led to changes in tumor growth and the distant spread of tumor cells, implying that stromal differences modulate the gene signatures and the proliferative and metastatic capabilities of pancreatic cancer cells.
• CAFs activate the MAPK and STAT3 signaling pathways in double-positive pancreatic cancer cells, and inhibitors of those pathways were more effective in cultures with high proportions of CAFs, with the greatest effects being produced by combining inhibitors of both pathways.
• Secretion of TGF-β by CAFs was found to drive the generation of double-positive PDACs, which provides a rationale for therapeutic agents that target TGF-β.
• Discrete tumor “glands,” comprised of clusters of PDACs, were more useful in predicting treatment outcomes than were individual cells, with glands consisting primarily of double-positive and metastatic/invasive cells associated with treatment resistance and poor patient survival. The prevalence of specific types of PDACs within tumor glands was influenced by the proportions of stromal to tumor cells within glands.

“The assay we developed to identify these different tumor glands provides a strategy to use it as a biomarker to select personalize therapy based on the response of normal cells to the cancer,” says Ting, who is an assistant professor of Medicine at Harvard Medical School. “The identification of the roles of both MAPK and STAT3 signaling in generating the different classes of PDACs and the role of CAF-secreted TGF-β in that signaling suggests the importance of investigating how different stromal compositions may determine the optimal drug combinations.”

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Martin Aryee, PhD, of the MGH Department of Pathology is co-senior author of the Cell paper, and the co-lead authors are Matteo Ligorio, MD, PhD, and Srinjoy Sil, MGH Cancer Center. Support for the study includes grants from Stand Up 2 Cancer, the Lustgarten Foundation, the National Science Foundation, the Hirshberg Foundation, and the American-Italian Cancer Foundation.

Massachusetts General Hospital, founded in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH Research Institute conducts the largest hospital-based research program in the nation, with an annual research budget of more than $925 million and major research centers in HIV/AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, genomic medicine, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, photomedicine and transplantation biology. The MGH topped the 2015 Nature Index list of health care organizations publishing in leading scientific journals and earned the prestigious 2015 Foster G. McGaw Prize for Excellence in Community Service. In August 2018 the MGH was once again named to the Honor Roll in the U.S. News & World Report list of “America’s Best Hospitals.”