New molecule may foresee the spread of breast cancer

Researchers have created a radioactive tracer molecule to identify myeloid-derived suppressor cells’ (MDSCs) accumulating in the lung before the arrival of breast cancer cells and shaping of metastases.

By using this new non-invasive imaging method, they can detect changes in the lungs that signal breast cancer may soon spread there – before any metastases are visible. If validated in humans, this approach could enable patients to be offered more intensive therapy earlier, to potentially prevent breast cancer spread. The study has been published in Theranostics, 

Previous research has shown that the gathering of a special type of immune cell MDSCs – in locations such as the lung – prepares the ground for breast cancer metastasis, by suppressing the local immune system and promoting the formation of angiogenesis.

To test this theory, they developed a tracer antibody able to attach itself to S100A8/A9, that can be detected using a special scan called SPECT (single photon emission computed tomography) – a 3D gamma-ray scanner. The tracer releases radiation which can be distinguished by the SPECT scanner, highlighting areas where S100A8/A9 molecules, and MDSCs, are accumulating. 

Previous research has shown that the gathering of a special type of immune cell called ‘myeloid-derived suppressor cells’ (MDSCs) – in locations such as the lung – prepares the ground for breast cancer metastasis, by suppressing the local immune system and promoting angiogenesis.

Currently, to assess the risk of a patient’s breast cancer spreading, doctors use tools based upon the features of the primary tumour, such as tumour size and whether it has already invaded nearby lymph nodes. With this early-stage study demonstrating the technique to be effective in mice, further studies are now required to develop a more effective ‘tracer’ molecule – better suited for use in humans – to be tested in clinical trials in future.

Dr Flores-Borja said: "By combining cell biology and imaging techniques, we have established a method to predict, at an early time-point during tumour development, whether tumour invasion will occur.  "We envision this technique being used to help select patients for either further surveillance or intensified therapy, as well as aiding cancer research. The development of a test that is able to identify an increased risk of metastasis soon after a patient is diagnosed with breast cancer, would be very useful in helping choose the best treatment for patients."

"This is a promising step towards being able to use 3D imaging to help offer more personalised therapy. Ultimately, anything that could provide patients and their doctors with a more accurate picture of whether their breast cancer may spread will help us tailor treatments to stop this from happening," she added.