(BBC) Three scientists who discovered how cells sense adapt to oxygen levels have won the 2019 Nobel Prize.
Sir Peter Ratcliffe, of the University of Oxford and Francis Crick Institute, William Kaelin, of Harvard, and Gregg Semenza, of Johns Hopkins University share the physiology or medicine prize.
Their work is leading to new treatments for anaemia and even cancer.
The role of oxygen-sensing is also being investigated in diseases from heart failure to chronic lung disease.
The Swedish Academy, which awards the prize, said: “The fundamental importance of oxygen has been understood for centuries but how cells adapt to changes in levels of oxygen has long been unknown.”
Oxygen levels vary in the body, particularly:
at high altitude
after a wound disrupts the blood supply
And when they drop, cells rapidly have to adapt their metabolism.
Why does this matter?
The oxygen-sensing ability of the body has a role in the immune system and the earliest stages of development inside the womb.
It can trigger the production of red blood cells or the construction of blood vessels.
So, drugs that mimic it may be an effective treatment for anaemia.
Tumours, meanwhile, can hijack this process to selfishly create new blood vessels and grow.
So, drugs that reverse it may help halt cancer.
“The work of these three scientists and their teams has paved the way to a greater understanding of these common, life-threatening conditions and new strategies to treat them,” Dr Andrew Murray, from the University of Cambridge, said.
“Congratulations to the three new Nobel Laureates. This is richly deserved.”
How was the discovery made?
Levels of hormone erythropoietin (EPO) were shown to rise as those of oxygen fell.
And the scientists discovered this was because a cluster of proteins called hypoxia-inducible factor (HIF) was changing the behaviour of DNA, the genetic code.
Further work showed when oxygen levels were normal, cells constantly produced HIF only for it to be destroyed by another protein, VHL.
But when oxygen levels fell, VHL could no longer stick to HIF, leading to the build-up sufficient levels to change the behaviour of DNA.