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3D Scaffold System May Lead to Novel Anticancer Therapies

저자:   업로드:2015-08-11  조회수:

    Scientists at Rice University and University of Texas MD Anderson Cancer Center have developed a way to mimic the conditions under which cancer tumors grow in bones. By placing cancer cells in a three-dimensional scaffold and subjecting them to the forces that push, pull, and continually flow through the body, the researchers are better able to test the efficiency of cancer-fighting drugs.


    The researchers discovered that bone tumors exposed to normal forces express more of a protein, insulin-like growth factor-1 (IGF-1), than detected in static cultures. The IGF-1 signaling pathway plays a critical role in resistance to current chemotherapy. The experiments were performed in a custom-made bioreactor by the Rice lab of bioengineer Antonios Mikos, Ph.D., in collaboration with the MD Anderson lab of Joseph Ludwig, M.D.


    The study (“Flow perfusion effects on three-dimensional culture and drug sensitivity of Ewing sarcoma”), detailed in the Proceedings of the National Academy of Sciences, shows the value of incorporating mechanical forces when modeling tumors and treatments as opposed to analyzing tumor growth statically, said lead author Marco Santoro, a chemical and biomolecular engineering graduate student of Mikos.


    "Mechanical forces are present in our bodies even though we are not always aware of them," he said. "Our cells are sensitive to the forces around them and change their behavior accordingly. Tumor cells behave the same way, changing their function depending on the forces they sense."


    Dr. Mikos and his team specialize in materials and strategies for tissue engineering and regenerative medicine. As part of that work, they have created foam-like materials that serve as scaffolds for cells to inhabit and grow into as they become new bone or tissue. That material provided an opportunity for the latest experiments at Rice's BioScience Research Collaborative on bone tumor samples called sarcomas provided by MD Anderson. Sarcoma tumors, also a focus of the Dr. Mikos lab, are most often found in the bones of adolescents and young adults.


    The researchers placed sarcoma cells in their porous, biologically inert scaffold and put the scaffold inside a flow perfusion bioreactor to mimic the stimulation those cells would experience amid the tissue inside real bone. They subjected the cells to biomechanical stimuli, including shear stress, by changing the fluid viscosity and flow rate.


    Over 10 days they found the steady flow of fluid through the scaffold prompted the sarcoma cells to proliferate throughout the structure. The higher shear stress helped the cells significantly increase their production of the IGF-1 protein and also down-regulated the production of two other cancer-related proteins, c-KIT and HER2, compared with static tests.


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