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Biologists who decoded how cells sense oxygen win medicine Nobel

William Kaelin, Peter Ratcliffe and Gregg Semenza share the award for discoveries that are crucial for understanding diseases such as cancer.

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Medicine Nobel prize winners 2019

William Kaelin (left), Peter Ratcliffe and Gregg Semenza (right) worked out how genes respond when oxygen is depleted.Credit: Harvard University/University of Oxford/Johns Hopkins Medicine

A trio of researchers has won the 2019 Nobel Prize in Physiology or Medicine for describing how cells sense and respond to changing oxygen levels by switching genes on and off — a discovery that has been key in understanding human diseases such as cancer and anaemia.

The three scientists are cancer researcher William Kaelin at the Dana-Farber Cancer Institute in Boston, Massachusetts; physician-scientist Peter Ratcliffe at the University of Oxford, UK, and the Francis Crick Institute in London; and geneticist Gregg Semenza at Johns Hopkins University in Baltimore, Maryland. The team also won the Albert Lasker Basic Medical Research Award in 2016.

Their work has helped researchers to understand how the body adapts to low oxygen levels by, for example, cranking out red blood cells and growing new blood vessels.

“This is a fundamental discovery that they’ve contributed to,” says Celeste Simon, a cancer biologist at the University of Pennsylvania in Philadelphia. “All organisms need oxygen, so it’s really important.”

“The field really coalesced around this discovery, which was dependent on each one of their findings,” says Randall Johnson, a physiologist at the University of Cambridge, UK, and the Karolinska Institute in Stockholm, and a member of the Nobel Assembly. “This really was a three-legged stool.”

Oxygen deprivation

The body’s tissues can be deprived of oxygen during exercise or when blood flow is interrupted, such as during a stroke. Cells’ ability to sense oxygen is also crucial for the proper growth of a developing fetus and placenta, and it’s also important for tumour growth, because the mass of rapidly growing cells can deplete oxygen in the interior of a tumour.

In work conducted in the 1990s, the scientists discovered the molecular processes that cells go through to respond to oxygen levels in the body. They found that central to this is a mechanism involving proteins called hypoxia-inducible factor (HIF) and VHL.

Semenza and Ratcliffe studied the regulation of a hormone called erythropoietin (EPO), which is crucial for stimulating the production of red blood cells in response to low levels of oxygen. Semenza and his team identified a pair of genes that encode the two proteins that form the protein complex HIF, which turns on certain genes and boosts EPO production when oxygen is low.

Meanwhile, Kaelin showed that a gene called VHL also seemed to be involved in how cells respond to oxygen. Kaelin was studying a genetic syndrome called von Hippel-Lindau’s disease; families with the disease carry mutations in VHL, and the condition raises the risk of certain cancers.

Ratcliffe and his team later found that the protein expressed by the VHL gene interacts with one of the components of HIF, turning off responses to low-oxygen conditions by marking the HIF component for destruction once oxygen levels rise.

And in 2001, teams led by Kaelin and Ratcliffe both elucidated more details about this process. They discovered that, when oxygen is present, a chemical modification to the VHL protein, called prolyl hydroxylation, allows VHL to bind to HIF, which leads to its breakdown. But this modification is blocked when cells are oxygen-starved, kick-starting the activity of HIF.

As a result, cells can react to low oxygen levels by simply blocking the breakdown of HIF, notes Mark Dewhirst, a cancer biologist at Duke University in Durham, North Carolina. “The cell can respond in minutes.”

Drug development

The work has led researchers to develop drugs that target oxygen-sensing processes, including those in cancer. Drugs, called prolyl hydroxylase inhibitors, that prevent VHL from binding to HIF and causing its degradation are also being investigated as treatments for anaemia and renal failure. Chinese regulators approved the first of these drugs in 2018.

“You could argue that some aspect of this is going to be germane to all diseases you can think of,” says Simon.

Colleagues hailed the trio as role models for other scientists. “They are extremely humble people,” says Dewhirst. “All three of them hold scientific rigour and reproducibility to the absolute highest standard,” adds Simon.

Kaelin, in particular, has taken his field to task for pursuing possible cancer treatments that aren’t backed up by strong evidence. “The most dangerous result in science is the one you were hoping for, because you declare victory and get lazy,” he told scientists at a 2018 talk at the US National Institutes of Health in Bethesda, Maryland.

In a 2017 essay in Nature, he offered some advice for peer reviewers: “The main question when reviewing a paper should be whether its conclusions are likely to be correct, not whether it would be important if it were true. Real advances are built with bricks, not straw.”

Nature 574, 161-162 (2019)

doi: 10.1038/d41586-019-02963-0

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