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Molecular Nevogenesis

Despite recent advances, the biology underlying nevogenesis remains unclear. Activating mutations in NRAS, HRAS, BRAF, and GNAQ have been identified in benign nevi. Their presence roughly correlates with congenital, Spitz, acquired, and blue nevi, respectively. These mutations are likely to play a c...

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Detalles Bibliográficos
Autores principales: Ross, Andrew L., Sanchez, Margaret I., Grichnik, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130972/
https://www.ncbi.nlm.nih.gov/pubmed/21754924
http://dx.doi.org/10.1155/2011/463184
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author Ross, Andrew L.
Sanchez, Margaret I.
Grichnik, James M.
author_facet Ross, Andrew L.
Sanchez, Margaret I.
Grichnik, James M.
author_sort Ross, Andrew L.
collection PubMed
description Despite recent advances, the biology underlying nevogenesis remains unclear. Activating mutations in NRAS, HRAS, BRAF, and GNAQ have been identified in benign nevi. Their presence roughly correlates with congenital, Spitz, acquired, and blue nevi, respectively. These mutations are likely to play a critical role in driving nevogenesis. While each mutation is able to activate the MAP kinase pathway, they also interact with a host of different proteins in other pathways. The different melanocytic developmental pathways activated by each mutation cause the cells to migrate, proliferate, and differentiate to different extents within the skin. This causes each mutation to give rise to a characteristic growth pattern. The exact location and differentiation state of the cell of origin for benign moles remains to be discovered. Further research is necessary to fully understand nevus development given that most of the same developmental pathways are also present in melanoma.
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spelling pubmed-31309722011-07-13 Molecular Nevogenesis Ross, Andrew L. Sanchez, Margaret I. Grichnik, James M. Dermatol Res Pract Review Article Despite recent advances, the biology underlying nevogenesis remains unclear. Activating mutations in NRAS, HRAS, BRAF, and GNAQ have been identified in benign nevi. Their presence roughly correlates with congenital, Spitz, acquired, and blue nevi, respectively. These mutations are likely to play a critical role in driving nevogenesis. While each mutation is able to activate the MAP kinase pathway, they also interact with a host of different proteins in other pathways. The different melanocytic developmental pathways activated by each mutation cause the cells to migrate, proliferate, and differentiate to different extents within the skin. This causes each mutation to give rise to a characteristic growth pattern. The exact location and differentiation state of the cell of origin for benign moles remains to be discovered. Further research is necessary to fully understand nevus development given that most of the same developmental pathways are also present in melanoma. Hindawi Publishing Corporation 2011 2011-04-06 /pmc/articles/PMC3130972/ /pubmed/21754924 http://dx.doi.org/10.1155/2011/463184 Text en Copyright © 2011 Andrew L. Ross et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ross, Andrew L.
Sanchez, Margaret I.
Grichnik, James M.
Molecular Nevogenesis
title Molecular Nevogenesis
title_full Molecular Nevogenesis
title_fullStr Molecular Nevogenesis
title_full_unstemmed Molecular Nevogenesis
title_short Molecular Nevogenesis
title_sort molecular nevogenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130972/
https://www.ncbi.nlm.nih.gov/pubmed/21754924
http://dx.doi.org/10.1155/2011/463184
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