How cancer abducts your immune cells 鈥� and what we can do about it
, Reader in Cancer Biology writing in . Read the fully illustrated .
Cancer cells play it dirty to get what they want. They are survival artists with a strong criminal streak. They surround themselves with a protective shield of extra-cellular material and then secure supply lines by attracting new blood vessels.
To achieve both of these aims, they set immune cells a honey trap by releasing attractants in the form of which lure immune cells to growing tumours. At the cancer site, the abducted immune cells release growth hormones to guide new blood vessels to the tumour and help build a protective shield.
Since immune cells are hard to come by, cancer cells benefit from sites of chronic inflammation or larger wounds in their close vicinity as both attract them. This explains why are linked to chronic inflammation. Two associations include chronic inflammation of the liver or the bacterial infection of the stomach by Heliobacter pylori. How cancer cells pull off this trick is, however, largely unknown.
A social network
A fascinating insight into the intricate social network of cancer cells in The EMBO Journal. Two British research teams based in Bristol and Edinburgh, and one Danish team based in Aarhus, report that pre-cancerous cells redirect immune cells from nearby wounds to help them grow. Cancer cells mimic the signals, which are normally released at sites of tissue damage, to pinch from inflamed wounds. Neutrophils are the most abundant (40% to 75%) and the first-responders at sites of tissue damage.
Nicole Antonio, Marie B酶nnelykke-Behrndtz and Laura Ward took advantage of the translucent stage of young zebrafish (a model organism in animal research) to capture videos of moving neutrophiles. To initiate this movement they induced clones of cancerous cells to grow in the zebrafish and then inflicted laser wounds adjacent to them. In the absence of cancer cells, the rapidly recruited neutrophils remained for up to four hours at the damaged site. However in the presence of cancer cells, they became distracted from the wound and visited the nearby clones.
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The team also provided evidence for a direct interaction between the abducted neutrophils and the malignant cells. During their 鈥渃hat鈥�, which lasted up to 90 minutes, the immune cells released a chemical known as prostaglandin E2 to stimulate growth of the nearby cancer colonies.
What of human risk
Their ground-breaking work raises, of course, the important question of whether human cancer cells pull off the same dirty trick.
It has that the ulceration of melanoma, the rarest but most deadliest form of skin cancer, is a bad prognostic indicator. So the teams then analysed human melanoma samples taken from patients with different degrees of ulceration. They found a 15-fold increase in neutrophils from samples taken from non-inflamed melanomas to moderately ulcerated lesions, and a 100-fold increase from non-inflamed to excessively ulcerated lesions.
This shows that some human cancer cells share the ability to abduct and misuse immune cells to their advantage. It also poses the question of whether cancer surgery could enable malignant cells to survive when wounds become inflamed. A indeed suggested that the use of anti-inflammatory drugs such as ketorolac given to patients before and after surgery leads to a lower recurrence of their breast tumours. Their exciting findings may also explain why , which blocks the production of prostaglandin E2 so efficiently, of developing several types of cancer.
The new observations could pave the way for new anti-cancer therapies if it were to be possible to turn the abducted neutrophils into a trojan horse which would kill pre-malignant cells. The high impact of their work illustrates also the power of international collaborations which are much more powerful than the sum of of individual contribution in science and cancer research.
Publication date: 1 July 2015