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Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies
Cutaneous melanoma is an aggressive tumor responsible for 90% of mortality related to skin cancer. In the recent years, the discovery of driving mutations in melanoma has led to better treatment approaches. The last decade has seen a genomic revolution in the field of cancer. Such genomic revolution...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193952/ https://www.ncbi.nlm.nih.gov/pubmed/34123788 http://dx.doi.org/10.3389/fonc.2021.635488 |
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author | Scatena, Cristian Murtas, Daniela Tomei, Sara |
author_facet | Scatena, Cristian Murtas, Daniela Tomei, Sara |
author_sort | Scatena, Cristian |
collection | PubMed |
description | Cutaneous melanoma is an aggressive tumor responsible for 90% of mortality related to skin cancer. In the recent years, the discovery of driving mutations in melanoma has led to better treatment approaches. The last decade has seen a genomic revolution in the field of cancer. Such genomic revolution has led to the production of an unprecedented mole of data. High-throughput genomic technologies have facilitated the genomic, transcriptomic and epigenomic profiling of several cancers, including melanoma. Nevertheless, there are a number of newer genomic technologies that have not yet been employed in large studies. In this article we describe the current classification of cutaneous melanoma, we review the current knowledge of the main genetic alterations of cutaneous melanoma and their related impact on targeted therapies, and we describe the most recent high-throughput genomic technologies, highlighting their advantages and disadvantages. We hope that the current review will also help scientists to identify the most suitable technology to address melanoma-related relevant questions. The translation of this knowledge and all actual advancements into the clinical practice will be helpful in better defining the different molecular subsets of melanoma patients and provide new tools to address relevant questions on disease management. Genomic technologies might indeed allow to better predict the biological - and, subsequently, clinical - behavior for each subset of melanoma patients as well as to even identify all molecular changes in tumor cell populations during disease evolution toward a real achievement of a personalized medicine. |
format | Online Article Text |
id | pubmed-8193952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81939522021-06-12 Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies Scatena, Cristian Murtas, Daniela Tomei, Sara Front Oncol Oncology Cutaneous melanoma is an aggressive tumor responsible for 90% of mortality related to skin cancer. In the recent years, the discovery of driving mutations in melanoma has led to better treatment approaches. The last decade has seen a genomic revolution in the field of cancer. Such genomic revolution has led to the production of an unprecedented mole of data. High-throughput genomic technologies have facilitated the genomic, transcriptomic and epigenomic profiling of several cancers, including melanoma. Nevertheless, there are a number of newer genomic technologies that have not yet been employed in large studies. In this article we describe the current classification of cutaneous melanoma, we review the current knowledge of the main genetic alterations of cutaneous melanoma and their related impact on targeted therapies, and we describe the most recent high-throughput genomic technologies, highlighting their advantages and disadvantages. We hope that the current review will also help scientists to identify the most suitable technology to address melanoma-related relevant questions. The translation of this knowledge and all actual advancements into the clinical practice will be helpful in better defining the different molecular subsets of melanoma patients and provide new tools to address relevant questions on disease management. Genomic technologies might indeed allow to better predict the biological - and, subsequently, clinical - behavior for each subset of melanoma patients as well as to even identify all molecular changes in tumor cell populations during disease evolution toward a real achievement of a personalized medicine. Frontiers Media S.A. 2021-05-28 /pmc/articles/PMC8193952/ /pubmed/34123788 http://dx.doi.org/10.3389/fonc.2021.635488 Text en Copyright © 2021 Scatena, Murtas and Tomei https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Scatena, Cristian Murtas, Daniela Tomei, Sara Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies |
title | Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies |
title_full | Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies |
title_fullStr | Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies |
title_full_unstemmed | Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies |
title_short | Cutaneous Melanoma Classification: The Importance of High-Throughput Genomic Technologies |
title_sort | cutaneous melanoma classification: the importance of high-throughput genomic technologies |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193952/ https://www.ncbi.nlm.nih.gov/pubmed/34123788 http://dx.doi.org/10.3389/fonc.2021.635488 |
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