What makes pancreatic cancer so aggressive? New study sheds light
Media contact: Nicole Fawcett, 734-764-2220 | Patients may contact Cancer AnswerLine™, 800-865-1125
ANN ARBOR, Mich. – New research from the University of Michigan Comprehensive Cancer Center helps explain why pancreatic cancer is so lethal, with fewer than a third of patients surviving even early stage disease.
The researchers found a gene known to be involved in nearly 90 percent of pancreatic cancers promotes cancer growth and spread. The gene, ATDC, plays a key role in how a tumor progresses from a preinvasive state to an invasive cancer to metastatic cancer.
“We know that patients with the earliest stage of pancreatic cancer have a survival rate of only 30 percent. This suggests that even in that very early stage of invasive cancer there are already cells that have spread to distant parts of the body,” says study author Diane M. Simeone, M.D., director of the Pancreatic Cancer Center at the University of Michigan Comprehensive Cancer Center.
“This study sheds important light on what it is about pancreatic cancer that makes it so aggressive early in the game,” she adds. The study appears Jan. 15 in Genes and Development.
Researchers used a mouse model to replicate pancreatic cancer as it appears in humans. They also studied pancreatic cancer tissue samples and samples of pre-invasive pancreatic lesions. They found ATDC was expressed in a subset of the pre-invasive cells and played a role in the development of pancreatic cancer stem cells, the small number of cells in a tumor that fuel its growth and spread. This suggests that ATDC promotes a tumor’s invasiveness and spread early in the course of disease.
The researchers suspect that ATDC may be a potent drug target. No drugs currently exist to target this pathway in part because researchers do not understand the crystal structure of the protein. Simeone’s team, working with the University of Michigan Center for Structural Biology has made crystals of the protein and begun to create a three-dimensional structure that they can use as a model for drug development.
Preliminary data suggests that ATDC may also play a role in other cancer types, including bladder, ovarian, colorectal and lung cancers and multiple myeloma. But, Simeone notes, it’s particularly critical to find new treatment options for pancreatic cancer. About 46,400 Americans will be diagnosed with pancreatic cancer this year, and more than 39,000 will die of the disease. Pancreatic cancer is expected to become the second-leading cause of cancer death in the United States by 2030.
Additional authors: Lidong Wang, Huibin Yang, Ethan V. Abel, Gina M. Ney, Phillip L. Palmbos, Filip Bednar, Yaqing Zhang, Jacob Leflein, Meghna Waghray, Scott Owens, John E. Wilkinson, Jayendra Prasad, Mats Ljungman, Andrew D. Rhim, Marina Pasca di Magliano
Funding: National Cancer Institute grant R01 CA131045, Rogel Family Pancreatic Cancer Research Fund
Reference: Genes and Development, Vol. 29, No. 2, Jan. 15, 2015
Learn more about Pancreatic Cancer Treatment
- Pancreatic Cancer Center
- Pancreatic Cancer: What Are My Risks?
- Identifying a Doctor and Facility When You Have Cancer
Learn more about Pancreatic Cancer Research
- Pancreatic Cancer Research
- Pancreatic Cancer Stem Cell Research
- Cell hunters: the quest to diagnose pancreatic cancer early