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The humble tadpole could provide the key to developing effective anti-skin cancer drugs, thanks to a groundbreaking discovery by researchers at the University of East Anglia (UEA).
The scientists have identified a compound which, when introduced into Xenopus Laevis tadpoles, blocks the movement of the pigment cells that give the tadpoles their distinctive markings and which develop into the familiar greenish-brown of the adult frog. It is the uncontrolled movement and growth of pigment cells (melanophore) in both tadpoles and humans that causes a particularly dangerous form of skin cancer. By blocking the migration of these cells, the development and spread of cancerous tumors can potentially be prevented.
The findings are the culmination of several years' work by the UEA team. This unconventional study, which was initiated with funding from the UK Medical Research Council, identifies for the first time an effective new man-made MMP (metalloproteinase) inhibitor, known as 'NSC 84093'.
The work was led by the University of East Anglia, in partnership with the John Innes Centre (JIC) and Pfizer.
"This is an exciting advance with implications in the fight against cancer," said lead author Dr. Grant Wheeler of UEA's School of Biological Sciences. "The next step is to test the compound in other species and, in the longer term, embark on the development of new drugs to fight skin cancer in humans."