Researchers have found a way to stop the spread of cancer in mice by blocking specific molecules of melanoma skin cancer.
Melanoma skin cancer tumours grow larger and are more likely to metastasize due to interactions between a pair of molecules, according to experiments in mice and human cells. These results may restore the potential for a type of cancer therapy previously abandoned in clinical trials.
Delving into the world of melanoma skin cancer
According to the American Cancer Society, melanoma accounts for about 1% of skin cancers, but causes a large majority of skin cancer deaths. Not many treatments exist to prevent melanoma from metastasizing.
A research team led by Associate Professor Beate Heissig at the University of Tokyo Institute of Medical Science, Japan, has studied tissue type plasminogen activator (tPA) for over a decade.
tPA is a protease, a small molecule that can cut proteins. tPA bonds to a larger protein that sits within the membrane barrier of animal cells, called low-density lipoprotein receptor-related protein 1 (LRP1).
Heissig’s research team proposes blocking the metastasis-promoting action of tPA by preventing it from connecting to LRP1. Mice without LRP1 had smaller tumours, even when researchers provided extra tPA.
Yousef Salama, first author of the research paper and postdoctoral researcher in Heissig’s lab explains: “The scientific community knows that tPA can interfere with the cell signals being studied for cancer immunotherapy. Blocking tPA could enhance the immune system’s action and potentially boost the effectiveness of cancer immunotherapy treatments.”
Controlling melanoma skin cancer and how much it spreads
In 2016, the research group discovered that mice given extra tPA had greater numbers of a specific type of cell. This same cell type usually increases within the melanoma tumours and can enhance tumour growth. Based on that potential connection, the current project was designed to investigate what role tPA might play in melanoma skin cancer.
When cancer cells metastasize, they use proteases to cut through the matrix of protein chains that holds healthy cells in place. When cancer cells arrive in a new part of the body and begin to form new tumours, they corrupt nearby cells to build a supportive home for themselves.
Clinical researchers have attempted to prevent metastasis by stopping proteases. However, completely blocking all proteases causes unintended side effects. No protease-based cancer therapy has succeeded in clinical trials.
Salama explains the therapy further: “Our vision is a cancer therapy that specifically prevents the interaction of LRP1 and tPA so that only the metastasis effect of the protease is stopped.
“Better understanding of the specific interactions of LRP1 and tPA will hopefully lead to protease cancer treatments that maintain the normal, healthy protease actions of tPA.”