...
首页> 外文期刊>Tumour biology : >The study of inducing apoptosis effect of fructose 1,6-bisphosphate on the papillary thyroid carcinoma cell and its related mechanism.
【24h】

The study of inducing apoptosis effect of fructose 1,6-bisphosphate on the papillary thyroid carcinoma cell and its related mechanism.

机译:1,6-二磷酸果糖诱导甲状腺乳头状癌细胞凋亡的作用及其相关机制的研究。

获取原文
获取原文并翻译 | 示例
           

摘要

This study aims to investigate the apoptosis-inducing effect of fructose 1,6-bisphosphate (F1,6BP) on the related mechanism of papillary thyroid carcinoma W3 and T cells. W3 cells were treated with F1,6BP alone or in combination with antioxidant catalase (CAT) or N-acetyl-L-cysteine (NAC). The changes of cell viability and cell nucleus morphology were examined by cell proliferation assay and Hoechst staining, and apoptosis levels of these cells were measured with flow cytometry. The changes of reactive oxygen species (ROS) level and the percentage of oxidized glutathione in total glutathione in W3 cells were detected by 2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA) staining or colorimetry assay. At the same time, real-time fluorescence quantitative PCR was adopted to evaluate the expression levels of CAT and glutathione peroxidase (GSH-Px) mRNAs in W3 cells. F1,6BP inhibited the growth of W3 cells significantly, coupling with an increase in intracellular ROS level and the percentage of oxidized glutathione in total glutathione. Typical apoptotic morphological changes of the cell nucleus happened. The apoptosis rate and GSH-Px and CAT mRNAs expression levels were upregulated after F1,6BP treatment. The antitumor effect of F1,6BP was significantly decreased after W3 cells were pretreated with NAC and CAT. F1,6BP can induce the apoptosis of W3 cells through upregulating the generation of ROS, especially the production of H2O2.
机译:本研究旨在探讨果糖1,6-二磷酸(F1,6BP)对甲状腺乳头状癌W3和T细胞相关机制的诱导凋亡作用。 W3细胞单独或与抗氧化剂过氧化氢酶(CAT)或N-乙酰基-L-半胱氨酸(NAC)联合用F1,6BP处理。通过细胞增殖测定和Hoechst染色检查细胞活力和细胞核形态的变化,并通过流式细胞术测量这些细胞的凋亡水平。通过2',7'-二氯二氢荧光素二乙酸酯(DCFH-DA)染色或比色法检测W3细胞中活性氧(ROS)水平的变化和氧化型谷胱甘肽在总谷胱甘肽中的百分比。同时,采用实时荧光定量PCR评估W3细胞中CAT和谷胱甘肽过氧化物酶(GSH-Px)mRNA的表达水平。 F1,6BP显着抑制W3细胞的生长,同时增加细胞内ROS水平和总谷胱甘肽中氧化型谷胱甘肽的百分比。发生典型的细胞核凋亡形态变化。 F1,6BP处理后细胞凋亡率,GSH-Px和CAT mRNA表达水平上调。 NAC和CAT预处理W3细胞后,F1,6BP的抗肿瘤作用明显降低。 F1,6BP可以通过上调ROS的产生,特别是过氧化氢的产生来诱导W3细胞的凋亡。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号