首页> 美国卫生研究院文献>The Korean Journal of Physiology Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology >Thrombin-induced Migration and Matrix Metalloproteinase-9 Expression Are Regulated by MAPK and PI3K Pathways in C6 Glioma Cells
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Thrombin-induced Migration and Matrix Metalloproteinase-9 Expression Are Regulated by MAPK and PI3K Pathways in C6 Glioma Cells

机译:凝血酶诱导的迁移和基质金属蛋白酶9表达受C6胶质瘤细胞中MAPK和PI3K途径的调节。

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摘要

Glioblastoma multiforme is one of the most common and aggressive tumors in central nervous system. It often possesses characteristic necrotic lesions with hemorrhages, which increase the chances of exposure to thrombin. Thrombin has been known as a regulator of MMP-9 expression and cancer cell migration. However, the effects of thrombin on glioma cells have not been clearly understood. In the present study, influences of thrombin on glioma cell migration were examined using Boyden chamber migration assay and thrombin-induced changes in MMP-9 expression were measured using zymography, semi-quantitative RT-PCR, and Western blotting. Furthermore, underlying signaling pathways by which thrombin induces MMP-9 expression were examined. Thrombin-induced migration and MMP-9 expression were significantly potentiated in the presence of wortmannin, a PI3K inhibitor, whereas MAPK inhibitors suppressed thrombin-induced migration and MMP-9 expression in C6 glioma cells. The present data strongly demonstrate that MAPK and PI3K pathways evidently regulate thrombin-induced migration and MMP-9 expression of C6 glioma cells. Therefore, the control of these pathways might be a beneficial therapeutic strategy for treatment of invasive glioblastoma multiforme.
机译:多形胶质母细胞瘤是中枢神经系统中最常见和侵袭性肿瘤之一。它通常具有特征性的坏死性病变并伴有出血,从而增加了接触凝血酶的机会。凝血酶已知是MMP-9表达和癌细胞迁移的调节剂。但是,尚不清楚凝血酶对神经胶质瘤细胞的作用。在本研究中,凝血酶对胶质瘤细胞迁移的影响使用Boyden室迁移测定法进行了检测,并通过酶谱法,半定量RT-PCR和Western印迹法检测了凝血酶诱导的MMP-9表达的变化。此外,检查了凝血酶诱导MMP-9表达的潜在信号通路。在PI3K抑制剂渥曼青霉素的存在下,凝血酶诱导的迁移和MMP-9表达显着增强,而MAPK抑制剂抑制凝血酶诱导的C6胶质瘤细胞中的迁移和MMP-9表达。本数据有力证明,MAPK和PI3K途径明显调节凝血酶诱导的C6胶质瘤细胞迁移和MMP-9表达。因此,控制这些途径可能是治疗浸润性胶质母细胞瘤的有益治疗策略。

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