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一种小分子端锚聚合酶抑制剂可降低胶质瘤干细胞的增殖和球状体形成。

A Small-Molecule Tankyrase Inhibitor Reduces Glioma Stem Cell Proliferation and Sphere Formation.

作者信息

Kierulf-Vieira Kirsten Strømme, Sandberg Cecilie Jonsgar, Waaler Jo, Lund Kaja, Skaga Erlend, Saberniak Birthe Mikkelsen, Panagopoulos Ioannis, Brandal Petter, Krauss Stefan, Langmoen Iver Arne, Vik-Mo Einar Osland

机构信息

Vilhelm Magnus Laboratory for Neurosurgical Research, Institute for Surgical Research and Department of Neurosurgery, Oslo University Hospital, P.O. Box 4950 Nydalen, 0424 Oslo, Norway.

Norwegian Stem Cell Center, Oslo University Hospital, University of Oslo, P.O. Box 1112 Blindern, 0317 Oslo, Norway.

出版信息

Cancers (Basel). 2020 Jun 19;12(6):1630. doi: 10.3390/cancers12061630.

Abstract

Evidence suggests that the growth and therapeutic resistance of glioblastoma (GBM) may be enabled by a population of glioma stem cells (GSCs) that are regulated by typical stem cell pathways, including the WNT/β-catenin signaling pathway. We wanted to explore the effect of treating GSCs with a small-molecule inhibitor of tankyrase, G007-LK, which has been shown to be a potent modulator of the WNT/β-catenin and Hippo pathways in colon cancer. Four primary GSC cultures and two primary adult neural stem cell cultures were treated with G007-LK and subsequently evaluated through the measurement of growth characteristics, as well as the expression of WNT/β-catenin and Hippo signaling pathway-related proteins and genes. Treatment with G007-LK decreased in vitro proliferation and sphere formation in all four primary GSC cultures in a dose-dependent manner. G007-LK treatment altered the expression of key downstream WNT/β-catenin and Hippo signaling pathway-related proteins and genes. Finally, cotreatment with the established GBM chemotherapeutic compound temozolomide (TMZ) led to an additive reduction in sphere formation, suggesting that WNT/β-catenin signaling may contribute to TMZ resistance. These observations suggest that tankyrase inhibition may serve as a supplement to current GBM therapy, although more work is needed to determine the exact downstream mechanisms involved.

摘要

有证据表明,胶质母细胞瘤(GBM)的生长和治疗抗性可能由一群受典型干细胞信号通路调控的胶质瘤干细胞(GSC)所驱动,这些信号通路包括WNT/β-连环蛋白信号通路。我们想要探究用端锚聚合酶小分子抑制剂G007-LK处理GSC的效果,该抑制剂已被证明是结肠癌中WNT/β-连环蛋白和Hippo信号通路的有效调节剂。用G007-LK处理4种原代GSC培养物和2种原代成人神经干细胞培养物,随后通过测量生长特性以及WNT/β-连环蛋白和Hippo信号通路相关蛋白及基因的表达进行评估。用G007-LK处理后,所有4种原代GSC培养物的体外增殖和球状体形成均呈剂量依赖性降低。G007-LK处理改变了关键下游WNT/β-连环蛋白和Hippo信号通路相关蛋白及基因的表达。最后,与已确立的GBM化疗药物替莫唑胺(TMZ)联合处理导致球状体形成进一步减少,这表明WNT/β-连环蛋白信号可能与TMZ抗性有关。这些观察结果表明,抑制端锚聚合酶可能作为当前GBM治疗的一种补充,不过还需要更多研究来确定其中确切的下游机制。

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