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Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities

Melanoma is characterised by its ability to metastasise at early stages of tumour development. Current clinico‐pathologic staging based on the American Joint Committee on Cancer criteria is used to guide surveillance and management in early‐stage disease, but its ability to predict clinical outcome...

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Detalles Bibliográficos
Autores principales: Rabbie, Roy, Ferguson, Peter, Molina‐Aguilar, Christian, Adams, David J, Robles‐Espinoza, Carla D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492003/
https://www.ncbi.nlm.nih.gov/pubmed/30511391
http://dx.doi.org/10.1002/path.5213
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author Rabbie, Roy
Ferguson, Peter
Molina‐Aguilar, Christian
Adams, David J
Robles‐Espinoza, Carla D
author_facet Rabbie, Roy
Ferguson, Peter
Molina‐Aguilar, Christian
Adams, David J
Robles‐Espinoza, Carla D
author_sort Rabbie, Roy
collection PubMed
description Melanoma is characterised by its ability to metastasise at early stages of tumour development. Current clinico‐pathologic staging based on the American Joint Committee on Cancer criteria is used to guide surveillance and management in early‐stage disease, but its ability to predict clinical outcome has limitations. Herein we review the genomics of melanoma subtypes including cutaneous, acral, uveal and mucosal, with a focus on the prognostic and predictive significance of key molecular aberrations. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
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spelling pubmed-64920032019-05-06 Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities Rabbie, Roy Ferguson, Peter Molina‐Aguilar, Christian Adams, David J Robles‐Espinoza, Carla D J Pathol Invited Reviews Melanoma is characterised by its ability to metastasise at early stages of tumour development. Current clinico‐pathologic staging based on the American Joint Committee on Cancer criteria is used to guide surveillance and management in early‐stage disease, but its ability to predict clinical outcome has limitations. Herein we review the genomics of melanoma subtypes including cutaneous, acral, uveal and mucosal, with a focus on the prognostic and predictive significance of key molecular aberrations. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2019-02-15 2019-04 /pmc/articles/PMC6492003/ /pubmed/30511391 http://dx.doi.org/10.1002/path.5213 Text en © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Reviews
Rabbie, Roy
Ferguson, Peter
Molina‐Aguilar, Christian
Adams, David J
Robles‐Espinoza, Carla D
Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
title Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
title_full Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
title_fullStr Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
title_full_unstemmed Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
title_short Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
title_sort melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
topic Invited Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492003/
https://www.ncbi.nlm.nih.gov/pubmed/30511391
http://dx.doi.org/10.1002/path.5213
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