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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Sigma-2 Receptors Play a Role in Cellular Metabolism: Stimulation of Glycolytic Hallmarks by CM764 in Human SK-N-SH Neuroblastomas
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Sigma-2 Receptors Play a Role in Cellular Metabolism: Stimulation of Glycolytic Hallmarks by CM764 in Human SK-N-SH Neuroblastomas

机译:Sigma-2受体在细胞代谢中发挥作用:在人SK-N-SH神经母细胞瘤中通过CM764刺激糖酵解标记。

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摘要

Sigma-2 receptors are attractive antineoplastic targets due to their ability to induce apoptosis and their upregulation in rapidly proliferating cancer cells compared with healthy tissue. However, this role is inconsistent with overexpression in cancer, which is typically associated with upregulation of prosurvival factors. Here, we report a novel metabolic regulatory function for sigma-2 receptors. CM764 [6-acetyl-3-(4-(4-(2-amino- 4-fluorophenyl) piperazin-1-yl)butyl) benzo[d]oxazol-2 (3H)-one] binds with K-i values of 86.6 +/- 2.8 and 3.5 +/- 0.9 nM at the sigma-1 and sigma-2 receptors, respectively. CM764 increased reduction of MTT [3-[4,5 dimethylthiazol-2-yl]-2,5 diphenyltetrazolium bromide] in human SK-N-SH neuroblastoma compared with untreated cells, an effect not due to proliferation. This effect was attenuated by five different sigma antagonists, including CM572 [3-(4-(4-(4-fluorophenyl) piperazin-1-yl) butyl)-6-isothiocyanatobenzo[ d] oxazol-2(3H)-one], which has no significant affinity for sigma-1 receptors. This effect was also observed in MG-63 osteosarcoma and HEK293T cells, indicating that this function is not exclusive to neuroblastoma or to cancer cells. CM764 produced an immediate, robust, and transient increase in cytosolic calcium, consistent with sigma-2 receptor activation. Additionally, we observed an increase in the total NAD(+)/NADH level and the ATP level in CM764-treated SK-N-SH cells compared with untreated cells. After only 4 hours of treatment, basal levels of reactive oxygen species were reduced by 90% in cells treated with CM764 over untreated cells, and HIF1 alpha and VEGF levels were increased after 3-24 hours of treatment. These data indicate that sigma-2 receptors may play a role in induction of glycolysis, representing a possible prosurvival function for the sigma-2 receptor that is consistent with its upregulation in cancer cells compared with healthy tissue.
机译:Sigma-2受体是诱人的抗肿瘤靶标,因为与健康组织相比,它们在快速增殖的癌细胞中具有诱导凋亡和上调的能力。但是,这种作用与癌症的过表达不一致,后者通常与生存因子的上调有关。在这里,我们报道了一种针对sigma-2受体的新型代谢调节功能。 CM764 [6-乙酰-3-(4-(4-(2-氨基-4-氟苯基)哌嗪-1-基)丁基)苯并[d]恶唑-2(3H)-one的Ki值为86.6在sigma-1和sigma-2受体处分别为+/- 2.8和3.5 +/- 0.9 nM。与未处理的细胞相比,CM764增加了人SK-N-SH神经母细胞瘤中MTT [3- [4,5二甲基噻唑-2-基] -2,5二苯基四唑溴化物]的减少,这种作用不是由于增殖引起的。五个不同的sigma拮抗剂(包括CM572 [3-(4-(4-(4-氟苯基)哌嗪-1-基)丁基] -6-异硫氰酸根合苯并[d]]恶唑-2(3H)-one])减弱了这种作用。对sigma-1受体没有明显的亲和力。在MG-63骨肉瘤和HEK293T细胞中也观察到了这种作用,表明该功能并非神经母细胞瘤或癌细胞所独有。 CM764产生了即时,稳定和短暂的胞质钙增加,与sigma-2受体激活一致。此外,我们观察到与未处理的细胞相比,CM764处理的SK-N-SH细胞的总NAD(+)/ NADH水平和ATP水平增加。在仅4小时的处理后,与未处理的细胞相比,用CM764处理的细胞中活性氧的基础水平降低了90%,并且在3-24小时的处理后,HIF1α和VEGF的水平增加。这些数据表明,sigma-2受体可能在糖酵解的诱导中发挥作用,代表sigma-2受体可能的生存功能,与健康组织相比,它在癌细胞中的上调是一致的。

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