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XBP1 对低氧环境下胶质瘤细胞活力及糖酵解的影响*
引用本文:柴双, 卞齐龙, 于涛, 欧阳仲瑞, 赵海杞, 刘珈杞, 侯旭, 赵世光, 刘耀华. XBP1 对低氧环境下胶质瘤细胞活力及糖酵解的影响*[J]. 中国肿瘤临床, 2016, 43(20): 892-897. DOI: 10.3969/j.issn.1000-8179.2016.20.588
作者姓名:柴双  卞齐龙  于涛  欧阳仲瑞  赵海杞  刘珈杞  侯旭  赵世光  刘耀华
作者单位:作者单位:哈尔滨医科大学附属第一医院神经外科(哈尔滨市150001)
基金项目:本文课题受国家自然科学基金项目(编号81372701)资助@@@@This work was supported by the National Nature Science Foundation of China (81372701)
摘    要:目的:明确低氧应激对胶质瘤细胞X-盒结合蛋白1(X-box binding protein1,XBP 1)的作用;明确胶质瘤细胞XBP 1 表达与糖代谢之间的关系;抑制XBP 1 表达对胶质瘤细胞在常氧和低氧环境下细胞活力的影响;明确低氧环境中XBP 1 对胶质瘤细胞糖酵解的影响。方法:分别在常氧和低氧条件下培养人脑胶质瘤细胞系,检测XBP 1 激活情况;使用siRNA 技术抑制XBP 1 表达,使用氧化磷酸化抑制剂处理细胞,检测细胞活力及糖代谢方式的改变,在常氧和低氧条件下检测细胞存活及糖酵解产物。结果:低氧环境下XBP 1 活化增加。低氧环境下XBP 1 沉默降低胶质瘤细胞活力、ATP 和乳酸生成,葡萄糖消耗量减少。细胞氧化磷酸化受到抑制后,XBP 1 沉默降低胶质瘤细胞存活率。结论:低氧环境可诱导胶质瘤细胞XBP 1 的活化。在低氧环境下XBP 1 沉默降低胶质瘤细胞活力和糖酵解,胶质瘤细胞的糖酵解依赖于XBP 1 活化。

关 键 词:XBP 1  胶质瘤  肿瘤能量代谢  糖酵解  低氧应激
收稿时间:2016-05-19
修稿时间:2016-08-04

Effects of XBP1 on glioma cell viability and glycolysis under hypoxia
Shuang CHAI, Qilong BIAN, Tao YU, Zhongrui OUYANG, Haiqi ZHAO, Jiaqi LIU, Xu HOU, Shiguang ZHAO, Yaohua LIU. Effects of XBP 1 on glioma cell viability and glycolysis under hypoxia[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(20): 892-897. DOI: 10.3969/j.issn.1000-8179.2016.20.588
Authors:Shuang CHAI  Qilong BIAN  Tao YU  Zhongrui OUYANG  Haiqi ZHAO  Jiaqi LIU  Xu HOU  Shiguang ZHAO  Yaohua LIU
Affiliation:Department of Neurosurgery, First Affiliated Hospital of Harbin Medical University, Harbin150001, China
Abstract:Objective:To determine the effect of hypoxic stress on glioma cell XBP1 expression, the relationship between XBP1 expres-sion and sugar metabolism, the influence of XBP1 repression on the survival rate of glioma cells under normoxia and hypoxia, and the influence of XBP1 on glioma cell glycolysis. Methods:We tested XBP1 activation in human glioma cell lines cultured under normoxia and hypoxia. XBP1 expression was repressed with siRNA technology. Cells were treated with oxidative phosphorylation inhibitor. We then detected the variation in cell apoptosis, sugar metabolism mode, and cell apoptosis and glycolysis products under normoxia and hypoxia. Results:XBP1 activation increased under hypoxia. Silencing XBP1 expression reduced glioma cell survival level, ATP and lactic acid production, and glucose consumption under hypoxia. After inhibiting cell oxidative phosphorylation, XBP1 repression significantly reduced the survival level of glioma cells. Conclusion:Hypoxia can activate XBP1 in glioma cells. Under hypoxia, XBP1 silencing de-presses cell activity and glycolysis. Glycolysis of glioma cells under hypoxia depends on XBP1 activation.
Keywords:XBP1  glioma  tumor metabolism  glycolysis  hypoxic stress
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