Low Doses of Radiation Promote Cancer-Capable Cells
Low doses of radiation equivalent to three CT scans, which are considered safe, give cancer-capable cells a competitive advantage over normal cells in healthy tissue, scientists have discovered. Researchers at the Wellcome Sanger Institute and the University of Cambridge studied the effects of low doses of radiation in the oesophagus of mice.
p53 mutant cell expansion in mouse oseophageal tissue (mutant cells in red and green).
The results, published today (18 July) in Cell Stem Cell show that low doses of radiation promote the spread of cancer-capable cells in healthy tissue. Researchers recommend that this risk should be considered in assessing radiation safety. The study also offers the possibility of developing non-toxic preventative measures to cut the risk of developing cancer by bolstering our healthy cells to outcompete and eradicate cancer-capable cells.
Every day we are exposed to various sources of ionising radiation, including natural radiation in soil and rock, and important medical procedures like CT scans and x-rays.
Low doses of radiation, such as the exposure from medical imaging, are considered safe as they cause little DNA damage and apparently minimal effect on long-term health. Until now, other effects of exposure to low levels of radiation have remained hidden, meaning understanding the true risk associated with low doses of radiation has been difficult.
Researchers have previously shown that our normal tissues, like skin, are battlefields where mutant cells compete for space against healthy cells. We all have cancer-capable mutant cells in healthy tissues, including those with p53 mutations, which increase in number as we age, yet very few eventually go on to form cancer.
In this new study, researchers show that low doses of radiation weigh the odds in favour of cancer-capable mutant cells in the oesophagus. The Sanger Institute researchers and their collaborators gave mice a 50 milligram dose of radiation, equivalent to three or four CT scans. As a result, the p53 mutant cells spread and outcompeted healthy cells.
“Our bodies are the set of ‘Game of Clones’ – a continuous battle for space between normal and mutant cells. We show that even low doses of radiation, similar to three CT scans’ worth, can weigh the odds in favour of cancer-capable mutant cells. We’ve uncovered an additional potential cancer risk as a result of radiation that needs to be recognised.” said Dr David Fernandez-Antoran, first author from the Wellcome Sanger Institute
Researchers then gave the mice an over-the-counter antioxidant – N-Acetyl Cysteine (NAC) – before exposure to the same level of radiation. The team discovered that the antioxidant gave normal cells the boost needed to outcompete and eradicate the p53 mutant cells.
However, the antioxidant alone without exposure to radiation did not help normal cells battle the mutant clones.
“Giving mice an antioxidant before exposing them to low doses of radiation gave healthy cells the extra boost needed to fight against the mutant cells in the oesophagus and make them disappear. However, we don’t know the effect this therapy would have in other tissues – it could help cancer-capable cells elsewhere become stronger. What we do know is that long term use of antioxidants alone is not effective in preventing cancer in people, according to other studies.” said Dr Kasumi Murai, an author from the Wellcome Sanger Institute
“Medical imaging procedures using radiation, such as CT scans and x-rays, have a very low level of risk – so low that it’s hard to measure. This research is helping us understand more about the effects of low doses of radiation and the risks it may carry. More research is needed to understand the effects in people.” saidProfessor Phil Jones, lead author from the Wellcome Sanger Institute and MRC Cancer Unit, University of Cambridge
The team suggests this research also highlights the possibility of developing therapies to prevent cancer. By making healthy cells fitter they naturally push out cancer-capable cells, without any toxic side effects for the patient.
Contacts and sources:
Dr Samantha Wynne
David Fernandez-Antoran, Gabriel Piedrafita, Kasumi Murai, Swee Hoe Ong, Albert Herms, Christian Frezza, Philip H. Jones. Cell Stem Cell, 2019; DOI: 10.1016/j.stem.2019.06.011
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