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In the Wnt-er of life: Wnt signalling in melanoma and ageing

Although the clinical landscape of melanoma is improving rapidly, metastatic melanoma remains a deadly disease. Age remains one of the greatest risk factors for melanoma, and patients older than 55 have a much poorer prognosis than younger individuals, even when the data are controlled for grade and...

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Detalles Bibliográficos
Autores principales: Kaur, Amanpreet, Webster, Marie R, Weeraratna, Ashani T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129830/
https://www.ncbi.nlm.nih.gov/pubmed/27764844
http://dx.doi.org/10.1038/bjc.2016.332
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author Kaur, Amanpreet
Webster, Marie R
Weeraratna, Ashani T
author_facet Kaur, Amanpreet
Webster, Marie R
Weeraratna, Ashani T
author_sort Kaur, Amanpreet
collection PubMed
description Although the clinical landscape of melanoma is improving rapidly, metastatic melanoma remains a deadly disease. Age remains one of the greatest risk factors for melanoma, and patients older than 55 have a much poorer prognosis than younger individuals, even when the data are controlled for grade and stage. The reasons for this disparity have not been fully uncovered, but there is some recent evidence that Wnt signalling may have a role. Wnt signalling is known to have roles both in cancer progression as well as in organismal ageing. In melanoma, the interplay of Wnt signalling pathways is complex, with different members of the Wnt family guiding different aspects of invasion and proliferation. Here, we will briefly review the current literature addressing the roles of different Wnt pathways in melanoma pathogenesis, provide an overview of Wnt signalling during ageing, and discuss the intersection between melanoma and ageing in terms of Wnt signalling.
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spelling pubmed-51298302016-12-16 In the Wnt-er of life: Wnt signalling in melanoma and ageing Kaur, Amanpreet Webster, Marie R Weeraratna, Ashani T Br J Cancer Minireview Although the clinical landscape of melanoma is improving rapidly, metastatic melanoma remains a deadly disease. Age remains one of the greatest risk factors for melanoma, and patients older than 55 have a much poorer prognosis than younger individuals, even when the data are controlled for grade and stage. The reasons for this disparity have not been fully uncovered, but there is some recent evidence that Wnt signalling may have a role. Wnt signalling is known to have roles both in cancer progression as well as in organismal ageing. In melanoma, the interplay of Wnt signalling pathways is complex, with different members of the Wnt family guiding different aspects of invasion and proliferation. Here, we will briefly review the current literature addressing the roles of different Wnt pathways in melanoma pathogenesis, provide an overview of Wnt signalling during ageing, and discuss the intersection between melanoma and ageing in terms of Wnt signalling. Nature Publishing Group 2016-11-22 2016-10-20 /pmc/articles/PMC5129830/ /pubmed/27764844 http://dx.doi.org/10.1038/bjc.2016.332 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Minireview
Kaur, Amanpreet
Webster, Marie R
Weeraratna, Ashani T
In the Wnt-er of life: Wnt signalling in melanoma and ageing
title In the Wnt-er of life: Wnt signalling in melanoma and ageing
title_full In the Wnt-er of life: Wnt signalling in melanoma and ageing
title_fullStr In the Wnt-er of life: Wnt signalling in melanoma and ageing
title_full_unstemmed In the Wnt-er of life: Wnt signalling in melanoma and ageing
title_short In the Wnt-er of life: Wnt signalling in melanoma and ageing
title_sort in the wnt-er of life: wnt signalling in melanoma and ageing
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129830/
https://www.ncbi.nlm.nih.gov/pubmed/27764844
http://dx.doi.org/10.1038/bjc.2016.332
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