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

被引:86
作者
Wang, Lifeng [1 ,3 ]
Liu, Na [1 ,3 ]
Yao, Libo [1 ,3 ]
Li, Fuyang [1 ,3 ]
Zhang, Jian [1 ,3 ]
Deng, Yanchun [1 ]
Liu, Junye [1 ,3 ]
Ji, Shaoping [1 ,3 ]
Yang, Angang [3 ]
Han, Hua [3 ]
Zhang, Yingqi [1 ,2 ,3 ]
Zhang, Jing [3 ]
Han, Wei [2 ,3 ]
Liu, Xinping [1 ,3 ]
机构
[1] Fourth Mil Med Univ, Dept Biochem & Mol Biol, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Biotechnol Ctr, Xian 710032, Peoples R China
[3] State Key Lab Canc Biol, Xian, Peoples R China
关键词
NDRG2; gene; hypoxia; HIF-1; apoptosis;
D O I
10.1159/000113765
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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. Copyright (c) 2008 S. Karger AG, Basel.
引用
收藏
页码:239 / 250
页数:12
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