Sigma receptors and cancer: Possible involvement of ion channels

被引:127
|
作者
Aydar, E [1 ]
Palmer, CP [1 ]
Djamgoz, MBA [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Biol Sci, London SW7 2AZ, England
关键词
D O I
10.1158/0008-5472.CAN-03-2329
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The sigma (or) receptor and its agonists have been implicated in a myriad of cellular functions, biological processes and diseases. Whereas the precise molecular mechanism(s) of sigma receptors and their involvement in cancer cell biology have not been elucidated, recent work has started to shed some light on these issues. A molecular model has been proposed for the cloned sigma1 receptor; the precise molecular nature of the sigma2 receptor remains unknown. sigma receptors have been found to be frequently up-regulated in human cancer cells and tissues. sigma2 receptor drugs particularly have been shown to have antiproliferative effects. An interesting possibility is that sigma and/or sigma1 drugs could produce anticancerous effects by modulating ion channels. As well as proliferation, a variety of other metastatic cellular behaviors such as adhesion, motility, and secretion may also be affected. Other mechanisms of sigma receptor action may involve interaction with ankyrin and modulation of intracellular Ca2+ and sphingolipid levels. Although more research is needed to further define the molecular physiology of or receptors, their involvement in the cellular pathophysiology of cancer raises the possibility that or drugs could be useful as novel therapeutic agents.
引用
收藏
页码:5029 / 5035
页数:7
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