Venturini Elisa, Leanza Luigi, Azzolini Michele, Kadow Stephanie, Mattarei Andrea, Weller Michael, Tabatabai Ghazaleh, Edwards Michael J, Zoratti Mario, Paradisi Cristina, Szabò Ildikò, Gulbins Erich, Becker Katrin Anne
Department of Molecular Biology, University of Duisburg-Essen, Essen, Germany.
Department of Biology, University of Padova, Padova, Italy.
Neurosignals. 2017;25(1):26-38. doi: 10.1159/000480643. Epub 2017 Sep 1.
BACKGROUND/AIMS: Glioblastoma (GBM) is one of the most aggressive cancers, counting for a high number of the newly diagnosed patients with central nervous system (CNS) cancers in the United States and Europe. Major features of GBM include aggressive and invasive growth as well as a high resistance to treatment. Kv1.3, a potassium channel of the shaker family, is expressed in the inner mitochondrial membrane of many cancer cells. Inhibition of mitochondrial Kv1.3 was shown to induce apoptosis in several tumor cells at doses that were not lethal for normal cells.
We investigated the expression of Kv1.3 in different glioma cell lines by immunocytochemistry, western blotting and electron microscopy and analyzed the effect of newly synthesized, mitochondria-targeted, Kv1.3 inhibitors on the induction of cell death in these cells. Finally, we performed in vivo studies on glioma bearing mice.
Here, we report that Kv1.3 is expressed in mitochondria of human and murine GL261, A172 and LN308 glioma cells. Treatment with the novel Kv1.3 inhibitors PAPTP or PCARBTP as well as with clofazimine induced massive cell death in glioma cells, while Psora-4 and PAP-1 were almost without effect. However, in vivo experiments revealed that the drugs had no effect on orthotopic brain tumors in vivo.
These data serve as proof of principle that Kv1.3 inhibitors kills GBM cells, but drugs that act in vivo against glioblastoma must be developed to translate these findings in vivo.
背景/目的:胶质母细胞瘤(GBM)是最具侵袭性的癌症之一,在美国和欧洲新诊断的中枢神经系统(CNS)癌症患者中占比很高。GBM的主要特征包括侵袭性生长以及对治疗的高度抗性。Kv1.3是一种摇椅家族的钾通道,在许多癌细胞的线粒体内膜中表达。线粒体Kv1.3的抑制作用已被证明在对正常细胞无致死性的剂量下可诱导多种肿瘤细胞凋亡。
我们通过免疫细胞化学、蛋白质印迹法和电子显微镜研究了Kv1.3在不同胶质瘤细胞系中的表达,并分析了新合成的、靶向线粒体的Kv1.3抑制剂对这些细胞中细胞死亡诱导的影响。最后,我们对荷胶质瘤小鼠进行了体内研究。
在此,我们报告Kv1.3在人源和鼠源GL261、A172和LN308胶质瘤细胞的线粒体中表达。用新型Kv1.3抑制剂PAPTP或PCARBTP以及氯法齐明处理可诱导胶质瘤细胞大量死亡,而补骨脂酚-4和PAP-1几乎没有效果。然而,体内实验表明这些药物对原位脑肿瘤没有作用。
这些数据证明了Kv1.3抑制剂可杀死GBM细胞,但必须开发出在体内对胶质母细胞瘤有效的药物,以便将这些发现转化到体内应用。