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T-Type Calcium Channels: A Potential Novel Target in Melanoma
T-type calcium channels (TTCCs) are overexpressed in several cancers. In this review, we summarize the recent advances and new insights into TTCC biology, tumor progression, and prognosis biomarker and therapeutic potential in the melanoma field. We describe a novel correlation between the Cav3.1 is...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072457/ https://www.ncbi.nlm.nih.gov/pubmed/32046241 http://dx.doi.org/10.3390/cancers12020391 |
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author | Barceló, Carla Sisó, Pol Maiques, Oscar de la Rosa, Inés Martí, Rosa M. Macià, Anna |
author_facet | Barceló, Carla Sisó, Pol Maiques, Oscar de la Rosa, Inés Martí, Rosa M. Macià, Anna |
author_sort | Barceló, Carla |
collection | PubMed |
description | T-type calcium channels (TTCCs) are overexpressed in several cancers. In this review, we summarize the recent advances and new insights into TTCC biology, tumor progression, and prognosis biomarker and therapeutic potential in the melanoma field. We describe a novel correlation between the Cav3.1 isoform and the increased basal autophagy in BRAF(V600E)-mutant melanomas and after acquired resistance to BRAF inhibitors. Indeed, TTCC blockers reduce melanoma cell viability and migration/invasion in vitro and tumor growth in mice xenografts in both BRAF-inhibitor-sensitive and -resistant scenarios. These studies open a new, promising therapeutic approach for disseminated melanoma and improved treatment in BRAFi relapsed melanomas, but further validation and clinical trials are needed for it to become a real therapeutic option. |
format | Online Article Text |
id | pubmed-7072457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70724572020-03-19 T-Type Calcium Channels: A Potential Novel Target in Melanoma Barceló, Carla Sisó, Pol Maiques, Oscar de la Rosa, Inés Martí, Rosa M. Macià, Anna Cancers (Basel) Review T-type calcium channels (TTCCs) are overexpressed in several cancers. In this review, we summarize the recent advances and new insights into TTCC biology, tumor progression, and prognosis biomarker and therapeutic potential in the melanoma field. We describe a novel correlation between the Cav3.1 isoform and the increased basal autophagy in BRAF(V600E)-mutant melanomas and after acquired resistance to BRAF inhibitors. Indeed, TTCC blockers reduce melanoma cell viability and migration/invasion in vitro and tumor growth in mice xenografts in both BRAF-inhibitor-sensitive and -resistant scenarios. These studies open a new, promising therapeutic approach for disseminated melanoma and improved treatment in BRAFi relapsed melanomas, but further validation and clinical trials are needed for it to become a real therapeutic option. MDPI 2020-02-08 /pmc/articles/PMC7072457/ /pubmed/32046241 http://dx.doi.org/10.3390/cancers12020391 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Barceló, Carla Sisó, Pol Maiques, Oscar de la Rosa, Inés Martí, Rosa M. Macià, Anna T-Type Calcium Channels: A Potential Novel Target in Melanoma |
title | T-Type Calcium Channels: A Potential Novel Target in Melanoma |
title_full | T-Type Calcium Channels: A Potential Novel Target in Melanoma |
title_fullStr | T-Type Calcium Channels: A Potential Novel Target in Melanoma |
title_full_unstemmed | T-Type Calcium Channels: A Potential Novel Target in Melanoma |
title_short | T-Type Calcium Channels: A Potential Novel Target in Melanoma |
title_sort | t-type calcium channels: a potential novel target in melanoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072457/ https://www.ncbi.nlm.nih.gov/pubmed/32046241 http://dx.doi.org/10.3390/cancers12020391 |
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