Researchers have unraveled how a cancer-critical enzyme sits on cell surfaces.
The enzyme enables tumor cells to tunnel through collagen, creating a convenient path for tumors to spread cancer throughout the body. The finding is an important step toward the development of pharmaceuticals that can prevent and treat the spreading of cancers in the body.
In order to spread cancer, tumor cells must make their way through collagen, which is the most abundant protein in the human body and provides structural strength to bones and tissue. One enzyme, which scientists have dubbed MT1-MMP, can “sit” on the surface of a tumor cell and digest the collagen in its path, opening a tunnel for tumor cells to spread.
The new results suggest that it may be possible to disrupt how this enzyme sits on a tumor cell, potentially blocking its ability to digest collagen and hindering the spread of cancer.
“The MT1-MMP enzyme has four ‘blades,’ like the blades on a propeller. Our study shows that two of the blades stick to tumor cells,” says Steven Van Doren, a professor of biochemistry in the College of Agriculture, Food and Natural Resources at the University of Missouri. “Because there are two blades, the enzyme can stick to the cell in two different ways. We found that one orientation allows the enzyme to digest the collagen while the other probably interferes with that process.”
Van Doren and his colleagues used an 800 MHz nuclear magnetic resonance spectrometer, the most powerful NMR spectrometer in the state of Missouri, to observe how the MT1-MMP enzyme bound itself to tumor cells. The spectrometer used radio waves to track the relevant molecules, allowing the researchers to identify the specific “blades” that are critical for binding to cells and digesting collagen.
Interfering in this enzyme’s digestion of collagen could close an important avenue for the spread of cancer through the body.
The researchers corroborated the conclusions with other measurements using fluorescent light. By shedding light on the specific positioning of these blades and the corresponding interactions with collagen, researchers have opened the door to interfering in this enzyme’s digestion of collagen, a strategy that could close an important avenue for the spread of cancer through the body.
“We now understand the importance of targeting enzymes like this one selectively,” Van Doren says. “This class of enzyme—metalloproteinases—had been studied decades ago, but the focus was too broad. As a result, the studies failed and these enzymes were neglected. Focusing specifically on the MT1-MMP enzyme allowed us to gather specific results that have practical applications for potential pharmaceuticals and further research.”
Van Doren says the next stage of research will be to identify compounds that can influence the positioning of the enzyme and block collagen digestion. Now that researchers better understand the enzyme, there are numerous potential applications not only for cancer research, but also for the treatment of arthritis to decrease joint damage and to decrease lung damage from the flu, according to Van Doren.
The study appears in Structure. Additional researchers who contributed to the work are from the University of Missouri, Tufts University, and Florida Atlantic University.
The National Institutes of Health provided funding for the study. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.
Source: University of Missouri
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