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Connexins in cancer: bridging the gap to the clinic
Gap junctions comprise arrays of intercellular channels formed by connexin proteins and provide for the direct communication between adjacent cells. This type of intercellular communication permits the coordination of cellular activities and plays key roles in the control of cell growth and differen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555763/ https://www.ncbi.nlm.nih.gov/pubmed/30814684 http://dx.doi.org/10.1038/s41388-019-0741-6 |
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author | Aasen, Trond Leithe, Edward Graham, Sheila V. Kameritsch, Petra Mayán, María D. Mesnil, Marc Pogoda, Kristin Tabernero, Arantxa |
author_facet | Aasen, Trond Leithe, Edward Graham, Sheila V. Kameritsch, Petra Mayán, María D. Mesnil, Marc Pogoda, Kristin Tabernero, Arantxa |
author_sort | Aasen, Trond |
collection | PubMed |
description | Gap junctions comprise arrays of intercellular channels formed by connexin proteins and provide for the direct communication between adjacent cells. This type of intercellular communication permits the coordination of cellular activities and plays key roles in the control of cell growth and differentiation and in the maintenance of tissue homoeostasis. After more than 50 years, deciphering the links among connexins, gap junctions and cancer, researchers are now beginning to translate this knowledge to the clinic. The emergence of new strategies for connexin targeting, combined with an improved understanding of the molecular bases underlying the dysregulation of connexins during cancer development, offers novel opportunities for clinical applications. However, different connexin isoforms have diverse channel-dependent and -independent functions that are tissue and stage specific. This can elicit both pro- and anti-tumorigenic effects that engender significant challenges in the path towards personalised medicine. Here, we review the current understanding of the role of connexins and gap junctions in cancer, with particular focus on the recent progress made in determining their prognostic and therapeutic potential. |
format | Online Article Text |
id | pubmed-6555763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65557632019-08-27 Connexins in cancer: bridging the gap to the clinic Aasen, Trond Leithe, Edward Graham, Sheila V. Kameritsch, Petra Mayán, María D. Mesnil, Marc Pogoda, Kristin Tabernero, Arantxa Oncogene Review Article Gap junctions comprise arrays of intercellular channels formed by connexin proteins and provide for the direct communication between adjacent cells. This type of intercellular communication permits the coordination of cellular activities and plays key roles in the control of cell growth and differentiation and in the maintenance of tissue homoeostasis. After more than 50 years, deciphering the links among connexins, gap junctions and cancer, researchers are now beginning to translate this knowledge to the clinic. The emergence of new strategies for connexin targeting, combined with an improved understanding of the molecular bases underlying the dysregulation of connexins during cancer development, offers novel opportunities for clinical applications. However, different connexin isoforms have diverse channel-dependent and -independent functions that are tissue and stage specific. This can elicit both pro- and anti-tumorigenic effects that engender significant challenges in the path towards personalised medicine. Here, we review the current understanding of the role of connexins and gap junctions in cancer, with particular focus on the recent progress made in determining their prognostic and therapeutic potential. Nature Publishing Group UK 2019-02-27 2019 /pmc/articles/PMC6555763/ /pubmed/30814684 http://dx.doi.org/10.1038/s41388-019-0741-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Article Aasen, Trond Leithe, Edward Graham, Sheila V. Kameritsch, Petra Mayán, María D. Mesnil, Marc Pogoda, Kristin Tabernero, Arantxa Connexins in cancer: bridging the gap to the clinic |
title | Connexins in cancer: bridging the gap to the clinic |
title_full | Connexins in cancer: bridging the gap to the clinic |
title_fullStr | Connexins in cancer: bridging the gap to the clinic |
title_full_unstemmed | Connexins in cancer: bridging the gap to the clinic |
title_short | Connexins in cancer: bridging the gap to the clinic |
title_sort | connexins in cancer: bridging the gap to the clinic |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555763/ https://www.ncbi.nlm.nih.gov/pubmed/30814684 http://dx.doi.org/10.1038/s41388-019-0741-6 |
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