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Direct association of high insulin levels and pancreatic cancer

Researchers at the University of British Columbia's (UBC) Faculty of Medicine has revealed a direct link between high insulin levels, common among patients with obesity and type 2 diabetes, and pancreatic cancer. According to the authors, this research the first detailed explanation of why people with obesity and type 2 diabetes are at an increased risk of pancreatic cancer. The research demonstrates that excessive insulin levels overstimulate pancreatic acinar cells, which produce digestive juices. This overstimulation leads to inflammation that converts these cells into precancerous cells.

Image legend: Pancreatic cancer cells (blue) growing as a sphere encased in membranes (red) (Credit: National Cancer Institute)

"Alongside the rapid increase in both obesity and type 2 diabetes, we're seeing an alarming rise in pancreatic cancer rates," said co-senior author of the paper, Dr James Johnson, a professor in the department of cellular and physiological sciences and interim director of the Life Sciences Institute at UBC. "These findings help us understand how this is happening, and highlights the importance of keeping insulin levels within a healthy range, which can be accomplished with diet, exercise and in some cases medications."


The study focused on pancreatic ductal adenocarcinoma (PDAC), the most prevalent pancreatic cancer, and one that is highly aggressive with a five-year survival rate of less than 10%. The incidence of pancreatic cancer is on the rise. By 2030, PDAC is expected to become the second leading cause of cancer-related deaths.


While obesity and type 2 diabetes had previously been established as risk factors for pancreatic cancer, the exact mechanisms by which this occurred remained unclear. This new study sheds light on the role of insulin and its receptors in this process.


"We found that hyperinsulinemia directly contributes to pancreatic cancer initiation through insulin receptors in acinar cells," said Dr. Anni Zhang, the study's first author from UBC. "The mechanism involves increased production of digestive enzymes, leading to heightened pancreatic inflammation."

While insulin is widely recognised for its role in regulating blood sugar levels, the study underscores its importance in pancreatic acinar cells. The findings show that insulin supports the physiological function of these cells in producing digestive enzymes that break down fat-rich foods, but at high levels, its increased action can inadvertently foster pancreatic inflammation and the development of precancerous cells.


The findings may pave the way for new cancer-prevention strategies and even therapeutic approaches that target insulin receptors in acinar cells.


"We hope this work will change clinical practice and help advance lifestyle interventions that can lower the risk of pancreatic cancer in the general population," said co-senior author, Dr Janel Kopp, assistant professor in the department of cellular and physiological sciences at UBC. "This research could also pave the way for targeted therapies that modulate insulin receptors to prevent or slow the progression of pancreatic cancer."


In collaboration with researchers at BC Cancer and the Pancreas Center BC, the team has initiated a clinical trial to help patients diagnosed with PDAC control their blood sugar and circulating insulin levels with the help of an endocrinologist.


The researchers say the findings may have implications for other cancers associated with obesity and type 2 diabetes, where elevated insulin levels may also play a contributing role in disease initiation.


"Colleagues in Toronto have shown similar connections between insulin and breast cancer," added Johnson. "In the future, we hope to determine whether and how excess insulin might contribute to other types of obesity- and diabetes-driven cancers."


The findings were published in the paper, ‘Hyperinsulinemia acts via acinar insulin receptors to initiate pancreatic cancer by increasing digestive enzyme production and inflammation’, published in Cell Metabolism.

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