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3-溴丙酮酸:一种新型靶向糖酵解药物,有望成为癌症治疗的新方法。

3-bromopyruvate: a new targeted antiglycolytic agent and a promise for cancer therapy.

机构信息

Russell H. Morgan Department of Radiology and Radiological Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

出版信息

Curr Pharm Biotechnol. 2010 Aug;11(5):510-7. doi: 10.2174/138920110791591427.

Abstract

The pyruvate analog, 3-bromopyruvate, is an alkylating agent and a potent inhibitor of glycolysis. This antiglycolytic property of 3-bromopyruvate has recently been exploited to target cancer cells, as most tumors depend on glycolysis for their energy requirements. The anticancer effect of 3-bromopyruvate is achieved by depleting intracellular energy (ATP) resulting in tumor cell death. In this review, we will discuss the principal mechanism of action and primary targets of 3-bromopyruvate, and report the impressive antitumor effects of 3-bromopyruvate in multiple animal tumor models. We describe that the primary mechanism of 3-bromopyruvate is via preferential alkylation of GAPDH and that 3-bromopyruvate mediated cell death is linked to generation of free radicals. Research in our laboratory also revealed that 3-bromopyruvate induces endoplasmic reticulum stress, inhibits global protein synthesis further contributing to cancer cell death. Therefore, these and other studies reveal the tremendous potential of 3-bromopyruvate as an anticancer agent.

摘要

丙酮酸类似物 3-溴丙酮酸是一种烷化剂和糖酵解的强抑制剂。3-溴丙酮酸的这种抗糖酵解特性最近被用于靶向癌细胞,因为大多数肿瘤依赖糖酵解来满足其能量需求。3-溴丙酮酸的抗癌作用是通过耗尽细胞内能量(ATP)导致肿瘤细胞死亡来实现的。在这篇综述中,我们将讨论 3-溴丙酮酸的主要作用机制和主要靶标,并报告 3-溴丙酮酸在多种动物肿瘤模型中的令人印象深刻的抗肿瘤效果。我们描述了 3-溴丙酮酸的主要机制是通过优先烷基化 GAPDH,并且 3-溴丙酮酸介导的细胞死亡与自由基的产生有关。我们实验室的研究还表明,3-溴丙酮酸诱导内质网应激,进一步抑制全球蛋白质合成,从而导致癌细胞死亡。因此,这些和其他研究揭示了 3-溴丙酮酸作为抗癌剂的巨大潜力。

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