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

Carrie D. House(George Washington University), Bi‐Dar Wang(George Washington University), Kristin Ceniccola(George Washington University), Russell Williams(George Washington University), May Simaan(National Institute of Dental and Craniofacial Research), Jacqueline Olender(George Washington University), Vyomesh Patel(National Institute of Dental and Craniofacial Research), Daniel T. Baptista‐Hon(University of Dundee), Christina M. Annunziata(National Cancer Institute), J. Silvio Gutkind(National Institute of Dental and Craniofacial Research), Tim G. Hales(University of Dundee), Norman H. Lee(George Washington University)
Scientific Reports
June 22, 2015
Cited by 96Open Access
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Abstract

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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