Scientists at the Ovarian Cancer Action Research Centre at Imperial College London have discovered a mechanism that deactivates ovarian cancer cells.

The findings, published in EMBO Reports, could lead to better treatments for women with ovarian cancer.

The research has found a new mechanism for a protein named OPCML. This protein is known as a tumor suppressor, as it prevents cells turning cancerous.

However OPCML is usually lost in cancer patients. Scientists have now found that when OPCML is put back into cancer cells, it cleverly deactivates a type of protein called AXL.

Previous research has shown the AXL protein accelerates the growth and spread of ovarian cancer cells. Clinical trials are already underway for treatments that block AXL, called AXL inhibitors.

But this new early-stage research demonstrates potential for minimizing treatment with AXL inhibitors, and in turn reducing side effects for women being treated for ovarian cancer.

When AXL becomes activated, it renders cancer cells more aggressive, increasing their ability to move and spread to other parts of the body.

However, it also reveals itself to OPCML, which then drags the bound molecules into a specific region of the cell where AXL is deactivated.

The research was funded by medical research charity Ovarian Cancer Action and carried out at the Ovarian Cancer Action Research Centre at Imperial College London.

The study, coauthored by Dr. Chiara Recchi and Professor Hani Gabra, found that since OPCML already blocks most of AXL, much less AXL inhibitor is required to deactivate the ovarian cancer cells.

Since inhibitors always present a certain degree of toxicity, if the dose of the inhibitor could be reduced, the patients should suffer fewer side effects.

The next stage is to develop OPCML as a therapeutic agent.

Since OPCML acts on the external part of the cells, delivering it on the surface of cancer cells could represent an efficient therapeutic strategy.

Also, OPCML is a “natural” protein present in most of the cells of our bodies, so it should have minimal toxicity.