Targeting potassium channels in cancer

被引:273
作者
Huang, Xi [1 ,2 ,3 ]
Jan, Lily Yeh [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
关键词
GATED SODIUM-CHANNELS; CELL-CYCLE; K+ CHANNELS; ION CHANNELS; SURFACE EXPRESSION; EPITHELIAL-CELLS; DNA METHYLATION; KV1.3; CHANNELS; GENE PROMOTER; TRP CHANNELS;
D O I
10.1083/jcb.201404136
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Potassium channels are pore-forming transmembrane proteins that regulate a multitude of biological processes by controlling potassium flow across cell membranes. Aberrant potassium channel functions contribute to diseases such as epilepsy, cardiac arrhythmia, and neuromuscular symptoms collectively known as channelopathies. Increasing evidence suggests that cancer constitutes another category of channelopathies associated with dysregulated channel expression. Indeed, potassium channel-modulating agents have demonstrated antitumor efficacy. Potassium channels regulate cancer cell behaviors such as proliferation and migration through both canonical ion permeation-dependent and noncanonical ion permeation-independent Functions. Given their cell surface localization and well-known pharmacology, pharmacological strategies to target potassium channel could prove to be promising cancer therapeutics.
引用
收藏
页码:151 / 162
页数:12
相关论文
共 109 条
[1]   A novel inward-rectifying K+ current with a cell-cycle dependence governs the resting potential of mammalian neuroblastoma cells [J].
Arcangeli, A ;
Bianchi, L ;
Becchetti, A ;
Faravelli, L ;
Coronnello, M ;
Mini, E ;
Olivotto, M ;
Wanke, E .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489 (02) :455-471
[2]   Integrated Analysis of Drug-Induced Gene Expression Profiles Predicts Novel hERG Inhibitors [J].
Babcock, Joseph J. ;
Du, Fang ;
Xu, Kaiping ;
Wheelan, Sarah J. ;
Li, Min .
PLOS ONE, 2013, 8 (07)
[3]   hERG channel function: beyond long QT [J].
Babcock, Joseph J. ;
Li, Min .
ACTA PHARMACOLOGICA SINICA, 2013, 34 (03) :329-335
[4]   Control of human potassium channel inactivation by editing of a small mRNA hairpin [J].
Bhalla, T ;
Rosenthal, JJC ;
Holmgren, M ;
Reenan, R .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (10) :950-956
[5]   The Intermediate Conductance Calcium-activated Potassium Channel KCa3.1 Regulates Vascular Smooth Muscle Cell Proliferation via Controlling Calcium-dependent Signaling [J].
Bi, Dan ;
Toyama, Kazuyoshi ;
Lemaitre, Vincent ;
Takai, Jun ;
Fan, Fan ;
Jenkins, David P. ;
Wulff, Heike ;
Gutterman, David D. ;
Park, Frank ;
Miura, Hiroto .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (22) :15843-15853
[6]   Voltage-Dependent Potassium Channels Kv1.3 and Kv1.5 in Human Cancer [J].
Bielanska, J. ;
Hernandez-Losa, J. ;
Perez-Verdaguer, M. ;
Moline, T. ;
Somoza, R. ;
Ramon y Cajal, S. ;
Condom, E. ;
Ferreres, J. C. ;
Felipe, A. .
CURRENT CANCER DRUG TARGETS, 2009, 9 (08) :904-914
[7]   CATION-TRANSPORT AND GROWTH-REGULATION IN NEURO-BLASTOMA CELLS - MODULATIONS OF K+-TRANSPORT AND ELECTRICAL MEMBRANE-PROPERTIES DURING THE CELL-CYCLE [J].
BOONSTRA, J ;
MUMMERY, CL ;
TERTOOLEN, LGJ ;
VANDERSAAG, PT ;
DELAAT, SW .
JOURNAL OF CELLULAR PHYSIOLOGY, 1981, 107 (01) :75-83
[8]   Mammalian Cells Change Volume during Mitosis [J].
Boucrot, Emmanuel ;
Kirchhausen, Tomas .
PLOS ONE, 2008, 3 (01)
[9]   Deregulation of 2 Potassium Channels in Pancreas Adenocarcinomas Implication of KV1.3 Gene Promoter Methylation [J].
Brevet, Marie ;
Fucks, David ;
Chatelain, Denis ;
Regimbeau, Jean-Marc ;
Delcenserie, Richard ;
Sevestre, Henri ;
Ouadid-Ahidouch, Halima .
PANCREAS, 2009, 38 (06) :649-654
[10]   DNA Methylation of KV 1.3 Potassium Channel Gene Promoter is Associated with Poorly Differentiated Breast Adenocarcinoma [J].
Brevet, Marie ;
Haren, Nathalie ;
Sevestre, Henri ;
Merviel, Philippe ;
Ouadid-Ahidouch, Halima .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2009, 24 (1-2) :25-32