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

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作者
Carrie D. House
Bi-Dar Wang
Kristin Ceniccola
Russell Williams
May Simaan
Jacqueline Olender
Vyomesh Patel
Daniel T. Baptista-Hon
Christina M. Annunziata
J. Silvio Gutkind
Tim G. Hales
Norman H. Lee
机构
[1] The George Washington University,Department of Pharmacology and Physiology
[2] The National Institute of Dental and Craniofacial Research,Division of Neuroscience
[3] The Institute of Academic Anaesthesia,undefined
[4] Ninewells Hospital,undefined
[5] University of Dundee,undefined
[6] Women’s Malignancies Branch,undefined
[7] National Cancer Institute,undefined
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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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