期刊论文详细信息
FEBS Letters
Sodium channel protein expression enhances the invasiveness of rat and human prostate cancer cells
Djamgoz, Mustafa B.A2  Ke, Youqiang1  Foster, Christopher S1  Fraser, Scott P2  Smith, Paul1  Rhodes, Nicholas P3  Shortland, Adam P3 
[1] Department of Cellular and Molecular Pathology, University of Liverpool, Liverpool L69 3GA, UK;Department of Biology, Imperial College of Science, Technology and Medicine, London SW7 2AZ, UK;Department of Clinical Engineering, University of Liverpool, Liverpool L69 3GA, UK
关键词: Prostatic carcinoma;    Flow cytometry;    Na+ channel;    Metastasis;    Tissue culture;   
DOI  :  10.1016/S0014-5793(98)00050-7
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

Expression of Na+ channel protein was analysed in established cell lines of rat and human prostatic carcinoma origin by flow cytometry using a fluorescein-labelled polyclonal antibody. In many cell lines examined, the obtained frequency distribution profiles were bimodal and identified a subpopulation of cells which expressed high levels of Na+ channel protein. A significant positive correlation was demonstrated between the proportion of channel-expressing cells and the functional ability of individual cell lines to invade a basement membrane matrix in vitro. In addition, two transfectant cell lines containing rat prostate cancer genomic DNA were found to express significantly elevated levels of Na+ channel protein when compared with the original benign recipient cell line. Enhanced Na+ channel expression by two metastatic derivatives of these transfectant cells directly correlated with increased invasiveness in vitro. These studies strongly support the hypothesis that expression of Na+ channel protein and the metastatic behaviour of prostatic carcinoma cells are functionally related, either by endowing the membranes of these cells with specialised electrophysiological properties (e.g. enhancing their motility and/or secretory activities) and/or by perturbing endogenous mechanisms regulating ionic homeostasis within the cells.

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