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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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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. |
format | Online Article Text |
id | pubmed-3130972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT rossandrewl molecularnevogenesis AT sanchezmargareti molecularnevogenesis AT grichnikjamesm molecularnevogenesis |