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Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling

Functional expression of voltage-gated Na(+) channels (VGSCs) has been demonstrated in multiple cancer cell types where channel activity induces invasive activity. The signaling mechanisms by which VGSCs promote oncogenesis remain poorly understood. We explored the signal transduction process critic...

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Autores principales: House, Carrie D., Wang, Bi-Dar, Ceniccola, Kristin, Williams, Russell, Simaan, May, Olender, Jacqueline, Patel, Vyomesh, Baptista-Hon, Daniel T., Annunziata, Christina M., Silvio Gutkind, J., Hales, Tim G., Lee, Norman H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476109/
https://www.ncbi.nlm.nih.gov/pubmed/26096612
http://dx.doi.org/10.1038/srep11541
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author House, Carrie D.
Wang, Bi-Dar
Ceniccola, Kristin
Williams, Russell
Simaan, May
Olender, Jacqueline
Patel, Vyomesh
Baptista-Hon, Daniel T.
Annunziata, Christina M.
Silvio Gutkind, J.
Hales, Tim G.
Lee, Norman H.
author_facet House, Carrie D.
Wang, Bi-Dar
Ceniccola, Kristin
Williams, Russell
Simaan, May
Olender, Jacqueline
Patel, Vyomesh
Baptista-Hon, Daniel T.
Annunziata, Christina M.
Silvio Gutkind, J.
Hales, Tim G.
Lee, Norman H.
author_sort House, Carrie D.
collection PubMed
description Functional expression of voltage-gated Na(+) channels (VGSCs) has been demonstrated in multiple cancer cell types where channel activity induces invasive activity. The signaling mechanisms by which VGSCs promote oncogenesis remain poorly understood. We explored the signal transduction process critical to VGSC-mediated invasion on the basis of reports linking channel activity to gene expression changes in excitable cells. Coincidentally, many genes transcriptionally regulated by the SCN5A isoform in colon cancer have an over-representation of cis-acting sites for transcription factors phosphorylated by ERK1/2 MAPK. We hypothesized that VGSC activity promotes MAPK activation to induce transcriptional changes in invasion-related genes. Using pharmacological inhibitors/activators and siRNA-mediated gene knockdowns, we correlated channel activity with Rap1-dependent persistent MAPK activation in the SW620 human colon cancer cell line. We further demonstrated that VGSC activity induces downstream changes in invasion-related gene expression via a PKA/ERK/c-JUN/ELK-1/ETS-1 transcriptional pathway. This is the first study illustrating a molecular mechanism linking functional activity of VGSCs to transcriptional activation of invasion-related genes.
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spelling pubmed-44761092015-06-24 Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling House, Carrie D. Wang, Bi-Dar Ceniccola, Kristin Williams, Russell Simaan, May Olender, Jacqueline Patel, Vyomesh Baptista-Hon, Daniel T. Annunziata, Christina M. Silvio Gutkind, J. Hales, Tim G. Lee, Norman H. Sci Rep Article Functional expression of voltage-gated Na(+) channels (VGSCs) has been demonstrated in multiple cancer cell types where channel activity induces invasive activity. The signaling mechanisms by which VGSCs promote oncogenesis remain poorly understood. We explored the signal transduction process critical to VGSC-mediated invasion on the basis of reports linking channel activity to gene expression changes in excitable cells. Coincidentally, many genes transcriptionally regulated by the SCN5A isoform in colon cancer have an over-representation of cis-acting sites for transcription factors phosphorylated by ERK1/2 MAPK. We hypothesized that VGSC activity promotes MAPK activation to induce transcriptional changes in invasion-related genes. Using pharmacological inhibitors/activators and siRNA-mediated gene knockdowns, we correlated channel activity with Rap1-dependent persistent MAPK activation in the SW620 human colon cancer cell line. We further demonstrated that VGSC activity induces downstream changes in invasion-related gene expression via a PKA/ERK/c-JUN/ELK-1/ETS-1 transcriptional pathway. This is the first study illustrating a molecular mechanism linking functional activity of VGSCs to transcriptional activation of invasion-related genes. Nature Publishing Group 2015-06-22 /pmc/articles/PMC4476109/ /pubmed/26096612 http://dx.doi.org/10.1038/srep11541 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
House, Carrie D.
Wang, Bi-Dar
Ceniccola, Kristin
Williams, Russell
Simaan, May
Olender, Jacqueline
Patel, Vyomesh
Baptista-Hon, Daniel T.
Annunziata, Christina M.
Silvio Gutkind, J.
Hales, Tim G.
Lee, Norman H.
Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling
title Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling
title_full Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling
title_fullStr Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling
title_full_unstemmed Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling
title_short Voltage-gated Na(+) Channel Activity Increases Colon Cancer Transcriptional Activity and Invasion Via Persistent MAPK Signaling
title_sort voltage-gated na(+) channel activity increases colon cancer transcriptional activity and invasion via persistent mapk signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476109/
https://www.ncbi.nlm.nih.gov/pubmed/26096612
http://dx.doi.org/10.1038/srep11541
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