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Mice with black fur that turns white? Specialist cancer researchers from Inserm, CNRS, the Institut Curie and the Université Paris-Sud have taken steps to better understand the development of skin cells responsible for pigmentation (known as melanocytes). By genetically manipulating mice with black fur, the researchers identified two key players: B-Raf and C-Raf proteins. These proteins are required for melanocyte stem cell self-maintenance and, as such, correct pigmentation throughout the mice’s life span. Without these two proteins, the mice’s fur turns white.
Their research is published in the review ‘Cell Report’ and paves the way for serious possibilities in terms of stopping the formation of melanomas, tumours that originate from melanocyte cells.
Melanocytes are cells in the organism used for skin, fur and hair pigment. This pigmentation function provides protection from the sun and lends organisms their colour. Malfunctions in these cells may lead to skin cancer known as melanoma. Melanomas are highly aggressive cancers that become very difficult to treat as they develop and metastases occur.
A few years ago, researchers discovered that, in humans, the B-Raf gene (coding gene for protein of the same name) is mutated in more than 50% of melanoma. Spectacular progress has been made in recent years in the treatment of this cancer, thanks to the development of pharmacological inhibitors that target an enzyme: the B-Raf kinase.
In this new research, scientists have tried to understand how melanocytes function normally, to then understand their specific role in cancer. To this end B-Raf protein expression, then, in turn, C-Raf protein expression, were removed from mice with black fur (ideal to clearly see any changes in pigmentation).
Black mice that become white with age
No changes in pigmentation were observed for mice that only had their B-Raf or C-Raf expression removed by researchers from the line of cells producing melanocytes.
Mice that had both coding genes for B-Raf and C-Raf removed simultaneously had a normal colour at birth. However, they progressively lost their pigmentation as they grew. They turned grey from black, before becoming increasingly white.
A. Eychène / F. Bertrand (Institut Curie)
For Alain Eychène, the research team leader, “these observations represent a fault in melanocyte renewal. Since the colour black is present at birth, the pigment cells clearly exist. However, the progressive whitening of the fur, once B-Raf and C-Raf have been removed from the cell line, proves that both these proteins are required for melanocyte renewal”.
As is the case for all cells, melanocytes originate from stem cells; the latter are responsible for renewal during moulting. This research shows that it is specifically this population of stem cells alone that disappears progressively in mutant mice.
For Alain Eychène, “This is the first in vivo demonstration of the role of RAF proteins in the self-renewal of stem cells”.
The fact that B-Raf and C-Raf are both involved in controlling and renewing pigment stem cells represents another step towards understanding and treating melanoma. By blocking these proteins (using inhibitors) in patients undergoing treatment, it is possible that in time researchers will succeed in eliminating all cancerous stem cells, i.e. the likely cause behind cases of cancer reoccurrence.
Juan Iovanna (Inserm Research Director) and his colleagues at the Marseille Cancer Research Center (Inserm/CNRS/Aix Marseille Université/Institut Paoli-Calmettes), in close collaboration with the "Tumor identity cards (CIT)" program run by the Ligue nationale contre le cancer and the University of Wisconsin (United ...
In a study published on 1 April 2017 in the prestigious journal Cancer Discovery, research teams at Gustave Roussy, Inserm and Paris-Sud University demonstrate that analysing the molecular portrait of a malignant tumour makes it possible to identify the appropriate therapy and ...
B-Raf and C-Raf Are Requiredfor Melanocyte Stem Cell Self-Maintenance
Agathe Valluet,1,2,3,4,6 Sabine Druillennec,1,2,3,4,6 Céline Barbotin,1,2,3,4 Coralie Dorard,1,2,3,4 Anne H. Monsoro-Burq,1,2,3,4Magalie Larcher,1,2,3,4 Celio Pouponnot,1,2,3,4 Manuela Baccarini,5 Lionel Larue,1,2,3,4 and Alain Eychène1,2,3,4,*
1Institut Curie 2INSERM U1021 3CNRS UMR 3347 Centre Universitaire, Orsay F-91405, France 4Universite´ Paris Sud-11, F-91405 Orsay, France 5Center for Molecular Biology, University of Vienna, Max F. Perutz Laboratories, A-1030 Vienna, Austria