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膜去极化通道阻滞剂通过损害营养物质运输和未折叠蛋白/氨基酸反应诱导选择性神经胶质瘤细胞死亡。

Membrane-Depolarizing Channel Blockers Induce Selective Glioma Cell Death by Impairing Nutrient Transport and Unfolded Protein/Amino Acid Responses.

机构信息

Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Cancer Res. 2017 Apr 1;77(7):1741-1752. doi: 10.1158/0008-5472.CAN-16-2274. Epub 2017 Jan 13.

Abstract

Glioma-initiating cells (GIC) are considered the underlying cause of recurrences of aggressive glioblastomas, replenishing the tumor population and undermining the efficacy of conventional chemotherapy. Here we report the discovery that inhibiting T-type voltage-gated Ca and K channels can effectively induce selective cell death of GIC and increase host survival in an orthotopic mouse model of human glioma. At present, the precise cellular pathways affected by the drugs affecting these channels are unknown. However, using cell-based assays and integrated proteomics, phosphoproteomics, and transcriptomics analyses, we identified the downstream signaling events these drugs affect. Changes in plasma membrane depolarization and elevated intracellular Na, which compromised Na-dependent nutrient transport, were documented. Deficits in nutrient deficit acted in turn to trigger the unfolded protein response and the amino acid response, leading ultimately to nutrient starvation and GIC cell death. Our results suggest new therapeutic targets to attack aggressive gliomas. .

摘要

神经胶质瘤起始细胞(GIC)被认为是侵袭性神经胶质瘤复发的根本原因,它们补充肿瘤群体并削弱传统化疗的疗效。在这里,我们报告了一项发现,即抑制 T 型电压门控钙和钾通道可以有效地诱导 GIC 的选择性细胞死亡,并增加人神经胶质瘤原位小鼠模型中的宿主存活率。目前,尚不清楚这些影响通道的药物影响的确切细胞途径。然而,使用基于细胞的测定法以及整合的蛋白质组学、磷酸蛋白质组学和转录组学分析,我们确定了这些药物影响的下游信号事件。记录了细胞膜去极化和细胞内 Na 升高的变化,这破坏了 Na 依赖性营养物质转运。营养物质缺乏的缺陷反过来触发未折叠蛋白反应和氨基酸反应,最终导致营养饥饿和 GIC 细胞死亡。我们的结果表明了新的治疗靶点,以攻击侵袭性神经胶质瘤。

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