Scientists at Queen Mary University of London have discovered molecules in mice that reprogram healthy immune cells causing skin cancer to spread.
31 January 2019
The molecules, released by invasive skin cancer, could be targeted with inhibiting drugs to prevent this aggressive skin cancer coming back after treatment.
The findings of the Cancer Research UK-funded study are published in Cell, today (Thursday).
Professor Vicky Sanz-Moreno, lead author from Barts Cancer Institute, Queen Mary University of London, said: “This study highlights how cancer cells interact with and influence their surrounding environment to grow and spread. Developing treatments that target the chemicals that alter the immune system could help to prevent the spread of the disease.”
Researchers from Queen Mary looked at cells from the edges of invasive melanomas in mice and human tumour samples, to investigate the effects of a protein they produce - called Myosin II.
They found that high levels of Myosin II in these cells not only makes them more mobile, but also triggers the release of chemicals that reprogram the immune system.
These chemicals affect the surrounding healthy immune cells, called macrophages, and hijack their natural cancer-killing abilities. This means that instead of attacking the cancer cells, they end up helping them to survive.
Some of these chemicals also make tiny holes in the blood vessels, allowing cancer cells to escape into the bloodstream and to new areas of the body.
Researchers also found that one of the chemicals released by Myosin II-rich cells, called interleukin 1A, was key for making cancer cells more invasive. By blocking Myosin II activity with different drugs, they reduced the amount of interleukin 1A produced by melanoma cells in mice and human tumour samples.
Professor Sanz-Moreno explains: “By using therapeutic drugs that block either Myosin II activity or the release of interleukin 1A, we can make the tumour less invasive and slow its growth, making it easier to treat.”
Drugs that block Myosin II activity are already being used to treat diseases such as glaucoma, a progressive disease of the eye. Researchers are planning further lab studies to investigate whether drugs that block Myosin II could be combined with existing melanoma treatments.
Professor Richard Marais, director of the Cancer Research UK Manchester Institute, said: “These exciting findings show how the basic research that Cancer Research UK funds is helping us to understand cancer biology and develop effective treatments for cancer patients.
“When melanoma is removed, there’s always a chance that some cells could remain. What this study shows is that we may be able to develop treatments to stop those remaining cells from spreading after surgery, helping patients to survive for longer.”
Regional Activation of Myosin II in Cancer Cells Drives Tumor Progression via a Secretory Cross-Talk with the Immune Microenvironment, Cell
For media information, contact:Joel Winston