K+ channels and cell cycle progression in tumor cells

被引:45
|
作者
Ouadid-Ahidouch, Halima [1 ]
Ahidouch, Ahmed [1 ,2 ]
机构
[1] Univ Picardie Jules Verne, UFR Sci, SFR CAP SANTE FED 4231, Lab Cellular & Mol Physiol EA4667, Amiens, France
[2] Ibn Zohr Univ, Fac Sci, Dept Biol, Agadir, Morocco
来源
FRONTIERS IN PHYSIOLOGY | 2013年 / 4卷
关键词
K+ channels; cell cycle; tumor cell; cyclins; CDK; membrane potential; calcium; volume control; BREAST-CANCER CELLS; GO POTASSIUM CHANNELS; ION CHANNELS; HUMAN ETHER; PROGNOSTIC-SIGNIFICANCE; FUNCTIONAL INTERACTION; INDUCED PROLIFERATION; DOWN-REGULATION; GROWTH-CONTROL; PATCH-CLAMP;
D O I
10.3389/fphys.2013.00220
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
K+ ions play a major role in many cellular processes. The deregulation of K+ signaling is associated with a variety of diseases such as hypertension, atherosclerosis, or diabetes. K+ ions are important for setting the membrane potential, the driving force for Ca2+ influx, and regulate volume of growing cells. Moreover, it is increasingly recognized that K+ channels control cell proliferation through a novel signaling mechanisms triggered and modulated independently of ion fluxes. In cancer, aberrant expression, regulation and/or sublocalization of K+ channels can alter the downstream signals that converge on the cell cycle machinery. Various K+ channels are involved in cell cycle progression and are needed only at particular stages of the cell cycle. Consistent with this idea, the expression of Eagl and HERG channels fluctuate along the cell cycle. Despite of acquired knowledge, our understanding of K+ channels functioning in cancer cells requires further studies. These include identifying the molecular mechanisms controlling the cell cycle machinery. By understanding how K+ channels regulate cell cycle progression in cancer cells, we will gain insights into how cancer cells subvert the need for K+ signal and its downstream targets to proliferate.
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页数:8
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