Researchers from the UCLA School of Dentistry have discovered a key molecule that allows cancer stem cells to bypass the body's natural immune defences, spurring the growth and spread of head and neck squamous cell cancers.

Their study, conducted in mice, also demonstrates that inhibiting this molecule derails cancer progression and helps eliminate these stem cells.

Published in the journal Cell Stem Cell, the findings could help pave the way for more effective targeted treatments for this highly invasive type of cancer, which is characterised by frequent resistance to therapies, rapid metastasis and a high mortality rate.

Cancer stem cells, also known as tumour-initiating cells, are considered to be the source of cancerous tissues -- the cells that give rise to all other cancer cells.

Their ability to survive and proliferate in the early stages of cancer development, as well as during tumour growth and metastasis, suggests they have an intrinsic ability to evade detection by the body's immune surveillance system.

The researchers set out to better understand how and why this happens.

When the immune system is functioning properly, the body's natural infection-fighting T cells help to identify and ward off carcinogenic cells, foreign viruses and other invaders. However, it is known that some cancer cells elude this immune response using protein molecules on their surface known as "checkpoints," which bind to similar molecules on the T cells, essentially nullifying the immune cells' cancer-killing capabilities.

To help rectify this, immunotherapy drugs called checkpoint inhibitors can be administered; these drugs turn off the cancer cells' checkpoint receptors, allowing T cells to perform their normal job.

In several types of cancer, including melanoma and non-small cell lung cancer, this approach has proven effective, decreasing the size of tumours and slowing their spread.

Yet results for head and neck squamous cell carcinomas have been mixed, indicating that something else may be occurring that mutes the immune system's response.
To begin the study, the researchers tested a common checkpoint inhibitor that uses anti-PD1 antibodies on a well-defined mouse model of head and neck squamous cell carcinoma.

The drug, they found, did very little to slow the spread of cancer.

At the same time, they discovered that cancer stem cells in head and neck tumours had a notably elevated expression of the gene CD276, which encodes a protein molecule on the cell surface.

They also found that CD276 expression was highest along the outer layers of tumours, suggesting that the CD276 molecule functions as a checkpoint that shields both the stem cells and cells in the interior of the tumour from the body's T cell response to cancer.

Similar to the use of checkpoint inhibitors, the researchers next administered anti-CD276 antibodies to a mouse model of the disease to see if this treatment could turn off the checkpoint and inhibit the growth and spread of cancer.

After a month, they witnessed a significant decrease in the number of cancerous lesions and cancer stem cells.

"Not only did we see a reduction in cancer stem cells and tumours in our model when we introduced the CD276 antibodies, but we also noticed that the total number of tumours that metastasised to the lymph nodes was significantly reduced," said Dr Cun-Yu Wang, the study's corresponding author and a professor of oral biology and medicine.

"We were able to show that by blocking the gene CD276, we could effectively stop the growth of tumours derived from cancer stem cells."

Dr Paul Krebsbach, dean of the UCLA School of Dentistry and a study co-author said, "These findings suggest that by focusing our attention on the CD276 gene and the immune response process, there is the potential for promising preventive therapeutic approaches against head and neck squamous cell carcinoma."

Source: University of California- Los Angeles