Biomaterials bolster the battle against cancer

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Biomaterials bolster the battle against cancer

ASU research first to modulate immune system metabolism during chemotherapy

graphic illustration showing how a cancer vaccine at work

Above: ASU Assistant Professor Abhinav Acharya is developing technologies that will permit the simultaneous use of cancer vaccines and chemotherapy treatments. The new biomaterials-based microparticles and nanoparticles, represented at the center, are formulated to restore the metabolic chain or pathway that enables the body's dendritic cells, represented at left, to boost the immune system. They also act to break the metabolic chain that feeds the proliferation of cancer cells. Graphic by Rhonda Hitchcock-Mast/ASU

“A single form of treatment is often not sufficient to defeat a given form of cancer,” says Abhinav Acharya, an assistant professor of chemical engineering at Arizona State University. “We need a combinatorial approach, meaning the use of two or more therapies together.”

For example, the tandem application of chemotherapy with immunotherapy or vaccine use could be much more effective than either measure alone. But the problem, Acharya says, is that each of these therapies is so taxing on the human immune system that they can’t be deployed simultaneously with a patient.

Solving this problem is the focus of a new project that Acharya is leading with the support of a grant from the National Institutes of Health. He is developing the first biomaterials-based technologies to modulate the functions of immune system cells in a way that can enable safe and effective combinations of clinical treatments to battle melanoma, ovarian cancer and potentially many other ailments.

Acharya works at the interface of materials science and immunology in the School for Engineering of Matter, Transport and Energy, one of the six Ira A. Fulton Schools of Engineering at ASU. His research for this NIH project focuses on cancer vaccines and applying the functions of their two major components: antigens and adjuvants.

Antigens trigger the immune system to create antibodies that attack a specific pathogen or toxin. These substances might take the form of inactive components from the targeted pathogen itself or, in the case of Acharya’s work, drugs tailored to induce a desired defense response.

Adjuvants are salt- or emulsion-based vaccine components that stimulate and amplify the immune system’s response to the particular pathogen targeted by the antigens. In other words, antigens identify the foe and adjuvants fuel the fight.

Part of Acharya’s work is developing novel adjuvants based on polymeric biomaterials generated from central carbon metabolites. The resulting polymers act as a source of cellular nutrients, and they can be fabricated either as microparticles or nanoparticles depending on their purpose.

“If the particles are micron-sized, they mimic the size of bacteria. If they are nanoparticles, they mimic the size of viruses,” Acharya says. “In either case, the immune system sees this foreign material as a threat and tries to digest it.”

This act of consumption is the key to delivering biomaterial-based nutrients to the body’s immune system when it is dampened during chemotherapy treatment. These nutrients can restore the chemo-suppressed metabolic pathways that enable sentinel-like dendritic cells to sound the alarm and prompt T-cells, a form of white blood cells, to fight the cancer.

Alongside rescuing the metabolic processes that help boost the body’s defenses, another goal is to disrupt the equivalent pathways that feed cancer cells. This latter task shapes three aims of this project, which specifically seeks to improve skin cancer treatment.

The first aim is to formulate and deliver a drug that disrupts a particular enzyme in the metabolic pathway of cancer cell glycolysis, which is the conversion of glucose into adenosine triphosphate, or ATP, a key fuel for cellular life. Halting this energy production pathway starves the cancer of the energy it needs to proliferate.

The second aim is similarly to formulate and deliver a drug targeting an enzyme in the metabolic pathway of cancer cell glutaminolysis, which is another means to generate ATP and other cancer-sustaining molecules within a tumor.

“And the third aim is to demonstrate that we can achieve these formulations at a scale to permit production for clinical use,” Acharya says.

Challenges to this work include generating a T-cell response that is robust enough to operate effectively in the context of both chemotherapy and the nutrient-deficient environment that the enzyme-targeting technology is creating in and around a tumor. But Acharya is confident of success after positive initial tests with cancerous human tissue in a laboratory setting.

Additionally, his interdisciplinary view of research already points to other applications for the innovations emerging from the NIH project.

“This is really a platform technology, so we can develop metabolic-modifying biomaterials for many purposes,” he says. “We are working right now with Dr. Marion Curtis, an immunologist with the Mayo Clinic, to determine how to deploy this new technology against other types of cancers. As well, there may be new remedies for traumatic brain injuries and opportunities to better combat autoimmune diseases, rheumatoid arthritis, multiple sclerosis and so much more. The potential is very exciting.”

About The Author

Gary Werner

Gary Werner is a science writer for the Ira A. Fulton Schools of Engineering. Prior to joining Arizona State University, Gary served as communications director for a Washington state government agency, as a senior nonfiction editor for Penguin Books, and as a newspaper and magazine journalist. Gary earned bachelor’s degrees in journalism and in international affairs from the University of Colorado at Boulder, as well as a master’s degree in education from Northwest University. At the beginning of his career, Gary served for six years in the U.S. Navy’s Atlantic submarine fleet. Media Contact: gary.werner@asu.edu | (480) 727-5622 | Ira A. Fulton Schools of Engineering

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