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Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation.

作者信息

Fraser Scott P, Ozerlat-Gunduz Iley, Brackenbury William J, Fitzgerald Elizabeth M, Campbell Thomas M, Coombes R Charles, Djamgoz Mustafa B A

机构信息

Neuroscience Solutions to Cancer Research Group, Department of Life Sciences, Imperial College London, , South Kensington Campus, London SW7 2AZ, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2014 Feb 3;369(1638):20130105. doi: 10.1098/rstb.2013.0105. Print 2014 Mar 19.


DOI:10.1098/rstb.2013.0105
PMID:24493753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3917359/
Abstract

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/1f21a0abf258/rstb20130105-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/410faefdc4c9/rstb20130105-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/2e1b6cf34a46/rstb20130105-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/9bccf5d50ce7/rstb20130105-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/c13cc2b3fbbe/rstb20130105-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/2c2d9bf0b1cb/rstb20130105-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/1f21a0abf258/rstb20130105-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/410faefdc4c9/rstb20130105-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/2e1b6cf34a46/rstb20130105-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/9bccf5d50ce7/rstb20130105-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/c13cc2b3fbbe/rstb20130105-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/2c2d9bf0b1cb/rstb20130105-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12c/3917359/1f21a0abf258/rstb20130105-g6.jpg

相似文献

[1]
Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation.

Philos Trans R Soc Lond B Biol Sci. 2014-2-3

[2]
Molecular pharmacology of voltage-gated sodium channel expression in metastatic disease: clinical potential of neonatal Nav1.5 in breast cancer.

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[3]
Activity-dependent regulation of voltage-gated Na+ channel expression in Mat-LyLu rat prostate cancer cell line.

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[4]
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[5]
Voltage-gated sodium channels and metastatic disease.

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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Noncanonical roles of voltage-gated sodium channels.

Neuron. 2013-10-16

[2]
Functional expression of the voltage-gated Na⁺-channel Nav1.7 is necessary for EGF-mediated invasion in human non-small cell lung cancer cells.

J Cell Sci. 2013-8-28

[3]
Tumor Necrosis Factor alpha induced hypoexcitability in rat muscle evidenced in a model of ion currents and action potential.

Cytokine. 2013-8-2

[4]
NaV1.5 Na⁺ channels allosterically regulate the NHE-1 exchanger and promote the activity of breast cancer cell invadopodia.

J Cell Sci. 2013-7-31

[5]
A novel androgen signalling pathway uses dihydrotestosterone, but not testosterone, to activate the EGF receptor signalling cascade in prostate stromal cells.

Br J Pharmacol. 2013-10

[6]
Autonomic nerve development contributes to prostate cancer progression.

Science. 2013-7-12

[7]
Effects of estradiol on voltage-gated sodium channels in mouse dorsal root ganglion neurons.

Brain Res. 2013-3-6

[8]
Nuclear receptors and their selective pharmacologic modulators.

Pharmacol Rev. 2013-3-1

[9]
TGF-β1, released by myofibroblasts, differentially regulates transcription and function of sodium and potassium channels in adult rat ventricular myocytes.

PLoS One. 2013-2-5

[10]
Membrane receptor cross talk in steroidogenesis: recent insights and clinical implications.

Steroids. 2013-6

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