UCL News


Antisocial, invasive cells are the basis of cancer

11 December 2008

UCL (University College London) scientists have discovered the mechanism by which cells normally repel each other - a process sidestepped by cancer cells which go on to invade and conquer healthy regions of the body.

The findings, published in the journal Nature, suggest an alternative way in which cancer treatments might work in the future, if therapies can be targeted at the process of 'cell repulsion' to stop cancer cells from spreading and causing secondary tumours.

Cells typically produce localized protrusions which help them navigate their environment. When two cells meet, they normally retract their protrusions and change their direction of movement, effectively 'repelling' one another. This phenomenon, called contact inhibition of locomotion, was first discovered 50 years ago in a UCL laboratory experiment, and its failure was thought to contribute to the malignant invasion of cancer. But it took up to now to witness the process in action and pin down the mechanism.

The latest study led by Dr Roberto Mayor, UCL Cell and Developmental Biology, has captured the phenomenon 'in vivo' - in living tissue - and has identified the mechanism by which it works, suggesting possible new targets for future cancer therapies.

Dr Roberto Mayor says: "Contact inhibition of locomotion was first discovered by UCL Professor Michael Abercrombie more than 50 years ago, when he saw fibroblast cells under the microscope confront each other, retract their protrusions and change direction on contact. The failure of cells to repulse each other in this way was thought to play a role in the spread of cancer."

"However, until now the molecular basis of this process and whether it also occurred within the body was unknown. Our study of neural crest cells shows that these cells behave in exactly this way. When two migrating neural crest cells meet, they stop, collapse their protrusions and change direction. However, when a neural crest cell meets another cell type, it fails to behave as expected and instead invades the other tissue, in the same manner as metastatic cancer cells which migrate and go on to cause secondary tumours."

"Inhibition of a type of cell signalling - non-canonical Wnt signalling - is behind this behaviour, cancelling the normal repulsion you would expect between cells. Our discovery offers possible new targets for the future treatment of tumour metastasis - the spreading of cancer cells, one of the mostly deadly aspects of cancer."

Notes for Editors

1. To request an interview or find out more, please contact Dr Roberto Mayor on tel: +44 (0)20 7679 3323, email: r.mayor@ucl.ac.uk. Images are also available from Dr Mayor.

2. Alternatively, please contact Jenny Gimpel in the UCL Media Relations Office on tel: +44 (0)20 7679 9726, mobile: +44 (0)7747 565 056, out of hours +44 (0)7917 271 364, e-mail: j.gimpel@ucl.ac.uk.

3. 'Contact inhibition of locomotion in vivo controls neural crest directional migration', by C. Carmona-Fontaine, H.K. Matthews, S. Kuriyama, M. Moreno, G.A. Dunn, M. Parsons, C.D. Stern and R. Mayor, is published in the journal Nature and is embargoed to 18:00 UK time Wednesday 10 December 2008. Journalists can obtain copies of the paper by contacting the UCL Media Relations Office.

4. The study was funded by the MRC and BBSRC.