Sigma受体:最新进展和新的临床潜力

Wayne D Bowen
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引用次数: 233

摘要

最近的几项进展使人们对西格玛受体有了更好的了解。在这里,我们将重点介绍我们最近关于sigma-2受体细胞功能的发现,并讨论其可能的临床意义。sigma-2受体激动剂诱导各种细胞类型的细胞形态和凋亡的变化。Sigma-2受体的激活产生了短暂的和持续的[Ca++]i的增加,来源于不同的细胞内储存。这些[Ca++]i的变化和细胞毒性作用是由细胞内sigma-2受体介导的。Sigma-2激动剂诱导耐药癌细胞凋亡,增强DNA损伤剂的效力,下调p-糖蛋白mRNA的表达。因此,sigma-2受体激动剂可用于治疗耐药癌症。Sigma放射配体已用于肿瘤成像。我们还讨论了sigma-2拮抗剂如何预防典型抗精神病药的不可逆运动副作用。Sigma-2受体可能是一种新的细胞凋亡信号通路,参与细胞增殖和/或活力的调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sigma receptors: recent advances and new clinical potentials

Several recent advances are leading to a better understanding of sigma receptors. Here we focus on our recent findings regarding cellular functions of sigma-2 receptors and discuss their possible clinical implications. Agonists at sigma-2 receptors induced changes in cell morphology and apoptosis in various cell types. Sigma-2 receptor activation produced both transient and sustained increases in [Ca++]i, derived from different intracellular stores. These changes in [Ca++]i and cytotoxic effects are mediated by intracellular sigma-2 receptors. Sigma-2 agonists induced apoptosis in drug-resistant cancer cells, enhanced the potency of DNA damaging agents, and down-regulated expression of p-glycoprotein mRNA. Thus, sigma-2 receptor agonists may be useful in treatment of drug-resistant cancers. Sigma radioligands have been used in tumor imaging. We also discuss how sigma-2 antagonists might prevent the irreversible motor side effects of typical neuroleptics. Sigma-2 receptors may subserve a novel signalling pathway to apoptosis, involved in regulation of cell proliferation and/or viability.

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