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Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation
Although ion channels are increasingly being discovered in cancer cells in vitro and in vivo, and shown to contribute to different aspects and stages of the cancer process, much less is known about the mechanisms controlling their expression. Here, we focus on voltage-gated Na(+) channels (VGSCs) wh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917359/ https://www.ncbi.nlm.nih.gov/pubmed/24493753 http://dx.doi.org/10.1098/rstb.2013.0105 |
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author | Fraser, Scott P. Ozerlat-Gunduz, Iley Brackenbury, William J. Fitzgerald, Elizabeth M. Campbell, Thomas M. Coombes, R. Charles Djamgoz, Mustafa B. A. |
author_facet | Fraser, Scott P. Ozerlat-Gunduz, Iley Brackenbury, William J. Fitzgerald, Elizabeth M. Campbell, Thomas M. Coombes, R. Charles Djamgoz, Mustafa B. A. |
author_sort | Fraser, Scott P. |
collection | PubMed |
description | Although ion channels are increasingly being discovered in cancer cells in vitro and in vivo, and shown to contribute to different aspects and stages of the cancer process, much less is known about the mechanisms controlling their expression. Here, we focus on voltage-gated Na(+) channels (VGSCs) which are upregulated in many types of carcinomas where their activity potentiates cell behaviours integral to the metastatic cascade. Regulation of VGSCs occurs at a hierarchy of levels from transcription to post-translation. Importantly, mainstream cancer mechanisms, especially hormones and growth factors, play a significant role in the regulation. On the whole, in major hormone-sensitive cancers, such as breast and prostate cancer, there is a negative association between genomic steroid hormone sensitivity and functional VGSC expression. Activity-dependent regulation by positive feedback has been demonstrated in strongly metastatic cells whereby the VGSC is self-sustaining, with its activity promoting further functional channel expression. Such auto-regulation is unlike normal cells in which activity-dependent regulation occurs mostly via negative feedback. Throughout, we highlight the possible clinical implications of functional VGSC expression and regulation in cancer. |
format | Online Article Text |
id | pubmed-3917359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39173592014-03-19 Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation Fraser, Scott P. Ozerlat-Gunduz, Iley Brackenbury, William J. Fitzgerald, Elizabeth M. Campbell, Thomas M. Coombes, R. Charles Djamgoz, Mustafa B. A. Philos Trans R Soc Lond B Biol Sci Articles Although ion channels are increasingly being discovered in cancer cells in vitro and in vivo, and shown to contribute to different aspects and stages of the cancer process, much less is known about the mechanisms controlling their expression. Here, we focus on voltage-gated Na(+) channels (VGSCs) which are upregulated in many types of carcinomas where their activity potentiates cell behaviours integral to the metastatic cascade. Regulation of VGSCs occurs at a hierarchy of levels from transcription to post-translation. Importantly, mainstream cancer mechanisms, especially hormones and growth factors, play a significant role in the regulation. On the whole, in major hormone-sensitive cancers, such as breast and prostate cancer, there is a negative association between genomic steroid hormone sensitivity and functional VGSC expression. Activity-dependent regulation by positive feedback has been demonstrated in strongly metastatic cells whereby the VGSC is self-sustaining, with its activity promoting further functional channel expression. Such auto-regulation is unlike normal cells in which activity-dependent regulation occurs mostly via negative feedback. Throughout, we highlight the possible clinical implications of functional VGSC expression and regulation in cancer. The Royal Society 2014-03-19 /pmc/articles/PMC3917359/ /pubmed/24493753 http://dx.doi.org/10.1098/rstb.2013.0105 Text en http://creativecommons.org/licenses/by/3.0/ © 2014 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Fraser, Scott P. Ozerlat-Gunduz, Iley Brackenbury, William J. Fitzgerald, Elizabeth M. Campbell, Thomas M. Coombes, R. Charles Djamgoz, Mustafa B. A. Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
title | Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
title_full | Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
title_fullStr | Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
title_full_unstemmed | Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
title_short | Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
title_sort | regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917359/ https://www.ncbi.nlm.nih.gov/pubmed/24493753 http://dx.doi.org/10.1098/rstb.2013.0105 |
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