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The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma
Cutaneous melanoma (CM) is a very aggressive disease, often characterized by unresponsiveness to conventional therapies and high mortality rates worldwide. The identification of the activating BRAF(V600) mutations in approximately 50% of CM patients has recently fueled the development of novel small...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807361/ https://www.ncbi.nlm.nih.gov/pubmed/34080276 http://dx.doi.org/10.1002/1878-0261.13034 |
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author | Montico, Barbara Giurato, Giorgio Pecoraro, Giovanni Salvati, Annamaria Covre, Alessia Colizzi, Francesca Steffan, Agostino Weisz, Alessandro Maio, Michele Sigalotti, Luca Fratta, Elisabetta |
author_facet | Montico, Barbara Giurato, Giorgio Pecoraro, Giovanni Salvati, Annamaria Covre, Alessia Colizzi, Francesca Steffan, Agostino Weisz, Alessandro Maio, Michele Sigalotti, Luca Fratta, Elisabetta |
author_sort | Montico, Barbara |
collection | PubMed |
description | Cutaneous melanoma (CM) is a very aggressive disease, often characterized by unresponsiveness to conventional therapies and high mortality rates worldwide. The identification of the activating BRAF(V600) mutations in approximately 50% of CM patients has recently fueled the development of novel small‐molecule inhibitors that specifically target BRAF(V600) ‐mutant CM. In addition, a major progress in CM treatment has been made by monoclonal antibodies that regulate the immune checkpoint inhibitors. However, although target‐based therapies and immunotherapeutic strategies have yielded promising results, CM treatment remains a major challenge. In the last decade, accumulating evidence points to the aberrant expression of different types of noncoding RNAs (ncRNAs) in CM. While studies on microRNAs have grown exponentially leading to significant insights on CM biology, the role of circular RNAs (circRNAs) and long noncoding RNAs (lncRNAs) in this tumor is less understood, and much remains to be discovered. Here, we summarize and critically review the available evidence on the molecular functions of circRNAs and lncRNAs in BRAF(V600) ‐mutant CM and CM immunogenicity, providing recent updates on their functional role in targeted therapy and immunotherapy resistance. In addition, we also include an evaluation of several algorithms and databases for prediction and validation of circRNA and lncRNA functional interactions. |
format | Online Article Text |
id | pubmed-8807361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88073612022-02-04 The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma Montico, Barbara Giurato, Giorgio Pecoraro, Giovanni Salvati, Annamaria Covre, Alessia Colizzi, Francesca Steffan, Agostino Weisz, Alessandro Maio, Michele Sigalotti, Luca Fratta, Elisabetta Mol Oncol Review Cutaneous melanoma (CM) is a very aggressive disease, often characterized by unresponsiveness to conventional therapies and high mortality rates worldwide. The identification of the activating BRAF(V600) mutations in approximately 50% of CM patients has recently fueled the development of novel small‐molecule inhibitors that specifically target BRAF(V600) ‐mutant CM. In addition, a major progress in CM treatment has been made by monoclonal antibodies that regulate the immune checkpoint inhibitors. However, although target‐based therapies and immunotherapeutic strategies have yielded promising results, CM treatment remains a major challenge. In the last decade, accumulating evidence points to the aberrant expression of different types of noncoding RNAs (ncRNAs) in CM. While studies on microRNAs have grown exponentially leading to significant insights on CM biology, the role of circular RNAs (circRNAs) and long noncoding RNAs (lncRNAs) in this tumor is less understood, and much remains to be discovered. Here, we summarize and critically review the available evidence on the molecular functions of circRNAs and lncRNAs in BRAF(V600) ‐mutant CM and CM immunogenicity, providing recent updates on their functional role in targeted therapy and immunotherapy resistance. In addition, we also include an evaluation of several algorithms and databases for prediction and validation of circRNA and lncRNA functional interactions. John Wiley and Sons Inc. 2021-06-18 2022-02 /pmc/articles/PMC8807361/ /pubmed/34080276 http://dx.doi.org/10.1002/1878-0261.13034 Text en © 2021 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Montico, Barbara Giurato, Giorgio Pecoraro, Giovanni Salvati, Annamaria Covre, Alessia Colizzi, Francesca Steffan, Agostino Weisz, Alessandro Maio, Michele Sigalotti, Luca Fratta, Elisabetta The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma |
title | The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma |
title_full | The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma |
title_fullStr | The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma |
title_full_unstemmed | The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma |
title_short | The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma |
title_sort | pleiotropic roles of circular and long noncoding rnas in cutaneous melanoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807361/ https://www.ncbi.nlm.nih.gov/pubmed/34080276 http://dx.doi.org/10.1002/1878-0261.13034 |
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