Regulation of voltage-gated sodium channel expression in cancer: hormones, growth factors and auto-regulation
Author(s) -
Scott P. Fraser,
Iley OzerlatGunduz,
William J. Brackenbury,
Elizabeth M. Fitzgerald,
Thomas M. Campbell,
R. Charles Coombes,
Mustafa B.A. Djamgoz
Publication year - 2014
Publication title -
philosophical transactions of the royal society b biological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.753
H-Index - 272
eISSN - 1471-2970
pISSN - 0962-8436
DOI - 10.1098/rstb.2013.0105
Subject(s) - sodium channel , biology , cancer cell , hormone , regulation of gene expression , cancer , ion channel , transcription factor , cancer research , neuroscience , carcinogenesis , downregulation and upregulation , microbiology and biotechnology , endocrinology , chemistry , gene , genetics , receptor , organic chemistry , sodium
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.
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