“This is a new finding that extends previous knowledge in this field,” Dr. Korc said. “The key new feature here is that there is a panel of microRNAs that can be measured accurately in the plasma component of blood to determine if a patient has pancreatic cancer.”
Specifically, the IU research team found that an increased expression of miRNA-10b, -155, and -106b in plasma appears highly accurate in diagnosing pancreatic ductal adenocarcinoma. Pancreatic ductal adenocarcinoma is by far the most common type of pancreatic malignancy.
Dr. Korc and colleagues made the discovery by examining plasma, bile, pancreatic juice or a combination, which had been collected from 215 patients either immediately before or during an endoscopy.
Dr. Korc pointed out that additional studies are needed to confirm that a blood test could be an effective method of diagnosing pancreatic cancer.
“It may be possible to use a blood test to screen individuals who are at high risk for developing pancreatic cancer,” Dr. Korc said. “We are planning to conduct such studies. It will be important to identify additional markers and to assess how useful a panel of such markers would be for the early diagnosis of this cancer. Based on our findings, this test could also be useful to differentiate between pancreatic cancer and chronic pancreatitis.”
Such a marker would be an advance against metastatic pancreatic cancer because current treatments typically extend a person’s life for only six to 16 weeks. Pancreatic cancer is difficult to detect and diagnose because there are no noticeable signs or symptoms in the early stages and because the pancreas is hidden behind other organs such as the stomach, small intestine, liver, gallbladder, spleen and bile ducts.
Only 6 percent of people with the disease survive more than five years after diagnosis. According to the National Cancer Institute, there will be an estimated 46,420 new cases of pancreatic cancer and 39,590 deaths from the disease in 2014.
This research was funded, in part, by NIH grants R37-CA-075059 and 5K23DK095148.
Contributing to the study were IU School of Medicine researchers Gregory A. Cote, M.D., M.S.; A. Jesse Gore, Ph.D.; Samantha D. McElyea, M.S.; Laura E. Heathers, B.A.; Huiping Xu, Ph.D.; and Stuart Sherman, M.D.
Dr. Korc was named the inaugural Myles Brand Professor of Cancer Research in October 2011. The professorship was created to help physicians and scientists at the IU Simon Cancer Center to continue investigating devastating malignancies, such as pancreatic cancer, which claimed the life of Brand, the 16th president of Indiana University. Brand served as IU’s president from 1994 to 2002.
He is also director of the Center for Pancreatic Cancer Research. The center brings together nearly 50 basic scientists and clinicians who work to improve outcomes for pancreatic cancer patients.
Dr. Korc’s focus is on aberrant growth-factor signaling in pancreatic cancer and genetic mouse models of pancreatic cancer, with the goal of designing novel therapeutic strategies. He has published more than 280 peer-reviewed manuscripts, and he is internationally recognized for his seminal contributions to the understanding of the role of the epidermal growth factor receptor and transforming growth factor-beta in pancreatic cancer, work for which he earned a National Institutes of Health MERIT Award. The highly-selective MERIT Awards are presented to researchers who demonstrate superior competence and outstanding productivity in research endeavors.