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拓扑替康是多形性胶质母细胞瘤中 SUMOylation 的有效抑制剂,可改变细胞复制和代谢编程。

Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming.

机构信息

Stroke Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Wellcome Trust-Medical Research Council Stem Cell Institute, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

出版信息

Sci Rep. 2017 Aug 7;7(1):7425. doi: 10.1038/s41598-017-07631-9.

Abstract

Protein SUMOylation is a dynamic post-translational modification shown to be involved in a diverse set of physiologic processes throughout the cell. SUMOylation has also been shown to play a role in the pathobiology of myriad cancers, one of which is glioblastoma multiforme (GBM). As such, the clinical significance and therapeutic utility offered via the selective control of global SUMOylation is readily apparent. There are, however, relatively few known/effective inhibitors of global SUMO-conjugation. Herein we describe the identification of topotecan as a novel inhibitor of global SUMOylation. We also provide evidence that inhibition of SUMOylation by topotecan is associated with reduced levels of CDK6 and HIF-1α, as well as pronounced changes in cell cycle progression and cellular metabolism, thereby highlighting its putative role as an adjuvant therapy in defined GBM patient populations.

摘要

蛋白质 SUMOylation 是一种动态的翻译后修饰,已被证明参与了细胞内各种生理过程。SUMOylation 还被证明在多种癌症的病理生物学中发挥作用,其中之一是多形性胶质母细胞瘤(GBM)。因此,通过选择性控制全局 SUMOylation 提供的临床意义和治疗效用是显而易见的。然而,已知/有效的全局 SUMO 缀合的抑制剂相对较少。本文描述了拓扑替康作为一种新的全局 SUMOylation 抑制剂的鉴定。我们还提供了证据,表明拓扑替康抑制 SUMOylation 与 CDK6 和 HIF-1α 水平降低有关,以及细胞周期进程和细胞代谢的明显变化,从而突出了其作为特定 GBM 患者群体辅助治疗的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a0f/5547153/63f6df340fd3/41598_2017_7631_Fig1_HTML.jpg

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