Cold Spring Harbor, NY — Scientists at Cold Spring Harbor Laboratory (CSHL) have solved a mystery about how pancreatic cancer spreads following surgery in patients whose tumor is successfully removed.
After surgery, patients typically experience a two-week period during which their immune system is depleted as a result of a surge in post-operative stress hormone (cortisol) levels. With killer T-cell levels sagging, isolated, dormant cancer cells that have already traveled to the liver and possibly other organs via the bloodstream begin to grow or metastasize.
This post-operative period, suggests CSHL Professor Douglas Fearon, “offers a window during which efforts might be made to keep cortisol levels down and T cells strong so the patient’s own immune system can kill the cancer cells that have made their way to other parts of the body but until this point have been dormant.”
Surgery is usually not an option for pancreas cancer patients, since most are diagnosed after the primary tumor has metastasized. This helps explain why only 8 percent of those diagnosed are still alive after 5 years. But doctors have been puzzled by the poor outcome in patients who should do better: the minority whose tumor seems confined to the pancreas at the time of diagnosis, and thus qualify for surgery. In many such patients, the liver, inspected during the operation, appears cancer-free. Yet within two years, most of these patients develop lethal metastatic cancer, often in the liver.
Today in Science a team led by Fearon and Dr. Arnaud Pommier in his lab, explains that dormant cancer cells are already in the liver well before patients have their primary tumor removed. They are likely carried there by the bloodstream, having been shed by the primary tumor. Fearon estimates that in a typical patient, 14 million cancer cells pass through the liver every day.
The immune system can kill most of the cancer cells deposited in the liver, but often it isn’t completely effective. Fearon and others have discovered in recent years how the immune system can be tricked or hijacked by cancer cells. The new discovery is one example.
The immune system seeks out and destroys cancer cells by sensing proteins called MHC1 and CK19 that are present on the outer membrane of the cancer cells. Fearon’s team found that the cancer cells that have been lying dormant in the liver of pancreatic cancer patients don’t express these proteins, so killer T cells can’t find them. In situations such as post-operative surgical stress, where T cells in the liver are depleted, the dormant cancer cells start to express MHC1 and CK19 surface markers again and begin to divide, becoming seeds of metastatic lesions.
Lustgarten Foundation; Cedar Hill Foundation; NIH-National Cancer Institute; Philippe Foundation.
Pommier A et al, “Unresolved endoplasmic reticulum stress engenders immune-resistant, latent pancreatic cancer metastases” appears in Science May 17, 2018.
Founded in 1890, Cold Spring Harbor Laboratory has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. Home to eight Nobel Prize winners, the private, not-for-profit Laboratory employs 1,100 people including 600 scientists, students and technicians. The Meetings & Courses Program annually hosts more than 12,000 scientists. The Laboratory’s education arm also includes an academic publishing house, a graduate school and the DNA Learning Center with programs for middle and high school students and teachers. For more information, visit www.cshl.edu
Cancer Center Member
M.D., Johns Hopkins University School of Medicine, 1968