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硼替佐米联合阿糖胞苷协同诱导U937细胞系凋亡的机制

[Mechanism of apoptosis synergistically induced by bortezomib combined with cytarabine in U937 cell line].

作者信息

He Cong, DU Xin, DU Sheng-Hong, Jia Pei-Min, Tong Jian-Hua, Zhou Li

机构信息

National Key Laboratory of Medical Genomics, Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012 Dec;20(6):1356-60.

Abstract

This study was aimed to further explore the apoptosis-inducing effect of bortezomib combined with cytarabine (Ara-C) on U937 cell line. Proliferation and apoptosis in U937 cells treated with bortezomib and/or Ara-C were assessed by cell count. Cell cycle distribution and reactive oxygen species (ROS) production level were measured by using flow cytometry. Cell signaling pathway related to apoptosis was analyzed by Western blot. The results showed that 10 nmol/L bortezomib combined with 50 nmol/L Ara-C significantly inhibited U937 cell proliferation. These two drug combination synergistically induced apoptosis in U937 cells, significantly increased cellular ROS level, and up-regulated the expression of phosphorylated form of JNK and P38 and down-regulated phosphorylation of ERK. It is concluded that the apoptosis of U937 cells synergistically induced by bortezomib combined with low concentration Ara-C is possibly associated with up-regulation of phosphorylated form of JNK, P38 and down-regulation of phosphorylation of ERK induced by increase of ROS, resulting in decrease of mitochondrial potential.

摘要

本研究旨在进一步探讨硼替佐米联合阿糖胞苷(Ara-C)对U937细胞系的凋亡诱导作用。通过细胞计数评估硼替佐米和/或阿糖胞苷处理的U937细胞中的增殖和凋亡情况。使用流式细胞术测量细胞周期分布和活性氧(ROS)产生水平。通过蛋白质免疫印迹法分析与凋亡相关的细胞信号通路。结果显示,10 nmol/L硼替佐米联合50 nmol/L阿糖胞苷显著抑制U937细胞增殖。这两种药物联合使用可协同诱导U937细胞凋亡,显著提高细胞内ROS水平,并上调JNK和P38磷酸化形式的表达,下调ERK的磷酸化。结论是,硼替佐米联合低浓度阿糖胞苷协同诱导U937细胞凋亡可能与ROS增加诱导的JNK、P38磷酸化形式上调和ERK磷酸化下调有关,导致线粒体膜电位降低。

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