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NDRG2是A549细胞中缺氧诱导凋亡所必需的一种新的HIF-1靶基因。

NDRG2 is a new HIF-1 target gene necessary for hypoxia-induced apoptosis in A549 cells.

作者信息

Wang Lifeng, Liu Na, Yao Libo, Li Fuyang, Zhang Jiang, Deng Yanchun, Liu Junye, Ji Shaoping, Yang Angang, Han Hua, Zhang Yingqi, Zhang Jing, Han Wei, Liu Xinping

机构信息

Department of Biochemistry and Molecular Biology, The Fourth Military Medical University, Xi'an, PR China.

出版信息

Cell Physiol Biochem. 2008;21(1-3):239-50. doi: 10.1159/000113765. Epub 2008 Jan 16.

Abstract

The NDRG2 gene belongs to a family of N-Myc downstream-regulated genes (NDRGs) and is expressed in many normal tissues. NDRG2 gene expression has been shown to be regulated in the stress response of certain cells. However, its function is not yet fully understood. Many studies have demonstrated that hypoxia, one of the stress responses, induced apoptosis in several cell types. In the current study, we investigated NDRG2 involvement in hypoxia response and found that NDRG2 expression was markedly up-regulated in several tumor cell lines exposed to hypoxic conditions or similar stresses at the mRNA and protein level. We also observed that the expression of NDRG2 was regulated by Hypoxia-inducible factor 1 (HIF-1) in tumor cells under hypoxia. Three hypoxia-responsive elements (HREs) in the NDRG2 promoter were identified. HRE1 could directly bind Hif-1 in vivo. Importantly, we found that silencing or enforcing the expression of NDRG2 could strongly inhibit or increase apoptosis. In addition, our data also showed that Ndrg2 was able to be translocated from the cytoplasm to the nucleus, and the segment from 101 to 178 amino acids of Ndrg2 is responsible for its translocation. Taken together, this study suggests that NDRG2 is a Hif-1 target gene and closely related with hypoxia-induced apoptosis in A549 cells.

摘要

NDRG2基因属于N-Myc下游调控基因(NDRGs)家族,在许多正常组织中表达。已证明NDRG2基因表达在某些细胞的应激反应中受到调控。然而,其功能尚未完全明确。许多研究表明,应激反应之一的缺氧可诱导多种细胞类型发生凋亡。在本研究中,我们调查了NDRG2在缺氧反应中的作用,发现暴露于缺氧条件或类似应激的几种肿瘤细胞系中,NDRG2在mRNA和蛋白质水平均显著上调。我们还观察到,缺氧条件下肿瘤细胞中NDRG2的表达受缺氧诱导因子1(HIF-1)调控。在NDRG2启动子中鉴定出三个缺氧反应元件(HREs)。HRE1可在体内直接结合Hif-1。重要的是,我们发现沉默或增强NDRG2的表达可强烈抑制或增加细胞凋亡。此外,我们的数据还表明,Ndrg2能够从细胞质转移到细胞核,并且Ndrg2第101至178个氨基酸片段负责其转移。综上所述,本研究表明NDRG2是Hif-1的靶基因,与A549细胞中缺氧诱导的凋亡密切相关。

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