UC research points to potential new treatment for pancreatic cancer

Study looks at a combination treatment that could help patients with pancreatic cancer

As the next step in finding a potential targeted treatment for pancreatic cancer, researchers at the University of Cincinnati have published a new study revealing how a combination therapy may improve outcomes for patients with this disease.

The study, led by graduate research assistant Kombo N'Guessan, PhD, and Xiaoyang Qi, PhD, professor in the Division of Hematology Oncology at the UC College of Medicine, is published in the journal Molecular Therapy.

“These research findings will help us lead a clinical trial with a combination therapeutic approach to treat pancreatic cancer patients,” says Qi, corresponding author on the paper and a member of the UC Cancer Center.

Dr. Xiaoyang Qi in lab.

Xiaoyang Qi, PhD, says his latest research findings will help physicians lead a clinical trial with a combination therapeutic approach to treat pancreatic cancer patients. Photo credit/Colleen Kelley/UC Creative + Brand

Researchers in this study have found that using a therapeutic compound, called SapC-DOPS, a nanovesicle (or a nanotechnology drug delivery system) made of microscopic components of a cell, to deliver a combined biomarker target therapy and standard chemotherapy for pancreatic cancer may show benefit to patients.

"Only a small number of promising drugs target pancreatic cancer, which is the fourth-leading cause of cancer deaths, with a five-year survival of less than six percent," Qi says. "Pancreatic cancer is usually asymptomatic in the early stages, while frequently invading lymph nodes and the liver, and less often the lungs and visceral organs. Current treatments, including surgery, chemotherapy and radiation therapy, have failed to improve long-term survival.

pancreatic cancer cells

Pancreatic cancer cells. Courtesy of the National Institutes of Health. Credit/Min Yu/Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC

“We’ve discovered a drug-targetable biomarker (phosphatidylserine) for pancreatic cancer cells in previous studies, and one of the first line treatments for advanced pancreatic cancer is chemotherapy, but it only provides marginal improvements for patients. We wanted to see if we could use the current first line treatment in combination with the novel nanovesicle drug delivery to improve outcomes.” 

In the early 2000s, Qi developed SapC-DOPS, a combination of a cell protein, SapC, and a phospholipid, DOPS, that assembled into tiny cavities can selectively target cells and deliver therapies while sparing all other unaffected cells and tissues. In the past, he has studied that nanovesicle in cancer animal models looking at brain, lung, skin, prostate, blood, breast and pancreatic cancers. It is currently being studied in clinical trials for brain cancers.

In this study, researchers used both animal models and human cancer cells to test this theory and found that the combination of these therapies together helped to target the biomarker on cancer cell surface at various points in their life cycle, ultimately inhibiting tumor growth and potentially increasing survival, in comparison to the treatments alone.

“This study shows that the combination treatment using the nanovesicles and a standard chemotherapy could be beneficial for patients with pancreatic cancer, possibly extending lives and helping a subset of patients with cancer that don’t have many options,” Qi says.

Featured image at top: Xiaoyang Qi, PhD, working in his lab in the Vontz Center for Molecular Studies. Photo/Colleen Kelley/UC Creative + Brand

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The University of Cincinnati is classified as a Research 1 institution by the Carnegie Commission and is ranked in the National Science Foundation's Top-35 public research universities. UC's graduate students and faculty investigate problems and innovate solutions with real-world impact. Next Lives Here.

This research was funded by the Give Hope Foundation and Bearcats Against Cancer as well as the UC College of Medicine. Partial support was provided by the National Institutes of Health (R01CA190717 and T32CA236764).

Qi is listed as an inventor on the patent for SapC-DOPS technology that is the subject of this research. The development and commercialization of this technology has been licensed to Bexion Pharmaceuticals in which Qi holds a minor (less than 5%) equity interest.

Bexion was not involved in this research.

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