Monday, February 9, 2015

Cancer cell ‘memory’ of oxygen deprivation explains tumour spread

University of Liverpool. UK: Scientists at the University of Liverpool have shown that supplying cancer cells with more oxygen may not prevent them spreading around the body, as originally thought. Research, published in the journal, Oncogenesis, has shown that cells have a ‘memory’ of an oxygen deprived environment, which, despite them having access to oxygen in their current state, could still trigger the production of genes that degrade the structure holding them in one area of the body. 

It is thought that cells that have a plentiful supply of oxygen are less likely to spread around the body, but new findings from Liverpool have shown that cells, with previous experience of oxygen deprivation, can still produce the genes that help them move around the body.
Some of the genes that are produced as a result of oxygen deprivation are sticky; if they are less sticky than neighbouring cells, they can detach from the tumour and move towards the blood vessels, where they can attach to the vessel wall. 
Monitoring the environment
Dr Violaine See, from the University’s Institute of Translational Medicine, said: “Therapies targeting cancer spread are challenging due to the complexity of the way the process works and the high number of variables involved.
“Although tumours that are deprived of oxygen have previously been associated with increased aggressiveness as well as resistance to radio and chemotherapy, the understanding of a direct link between the level and duration of hypoxia and the individual steps involved in cancer spread was still missing.
“Our tests with animal cells show that even those cells that have good oxygen supply can ‘remember’ a previous environment where they did not have access oxygen; they may also be influenced by the capabilities of neighbouring cells, encouraging movement towards the blood vessels.”
The research highlights the need to monitor the cellular environment in the body to help predict the consequences of the cells’ history on their future behaviour and their potential response to therapies.
The research is published in Nature.