“MMP7 is known to make cancer cells more aggressive and likely to spread throughout the body,” Van Doren said. “We now understand that MMP7 signals to cancer cells to become more aggressive when the enzyme cuts off specific proteins as it binds to those cancer cells. Knowing this, we hopefully can find ways to prevent these enzymes from binding and signaling to these cancer cells in the first place. The end result could be a way to prevent cancer cells from spreading so rapidly.”
For the study, Van Doren and his research team, including lead author Stephen Prior, a postdoctoral fellow at MU, used a highly sophisticated piece of equipment called a Nuclear Magnetic Resonance (NMR) spectrometer to map the structure of assemblies containing MMP7. Functioning similarly to a magnetic resonance imaging (MRI) machine, the NMR spectrometer uses large magnets to allow scientists detect the nuclei of atoms in order to reconstruct detailed images of sub-microscopic enzymes. The researchers then study these 3D images to determine how these enzymes work within the body.
Additionally, Van Doren and his research team published a study investigating a sister enzyme, known as MMP14. In this study, Van Doren used the same NMR spectrometer to determine how MMP14 helps cancer spread throughout the body. He says this knowledge also will inform future research into ways to prevent the spread of cancer.
“MMP14 is the most important protein-cutting enzyme in terms of how cancer cells migrate throughout the body,” Van Doren said. “These enzymes essentially cut paths through the collagen meshwork of tissues in the body. By clearing paths through this collagen, the MMP14 enzyme enables tumor cells to move and spread. By understanding the structures of how these enzymes attack collagen and other proteins, we can find ways to block them from allowing cancer to spread.”