Zhang Guo, Zhu Hongxia, Wang Yihua, Yang Shangbin, Liu Mei, Zhang Wei, Quan Lanping, Bai Jinfeng, Liu Zhihua, Xu Ningzhi
Laboratory of Cell and Molecular Biology, National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing 100021, PR China.
Biol Chem. 2009 May-Jun;390(5-6):463-9. doi: 10.1515/BC.2009.060.
Aberrant expression of survivin has been shown to be regulated at the transcription level in cancer cells. In this study, we demonstrate that there are six putative binding sites of Krüppel-like factor 4 (KLF4) within the 2000-bp region upstream of the transcription start site of the human survivin gene. Luciferase reporter gene assays revealed that survivin promoter activity is repressed upon overexpression of KLF4 in EC9706 cells. A chromatin immunoprecipitation assay indicated that KLF4 indeed binds the survivin promoter in vivo. It specifically binds the site located at position -40 among the six binding sites as determined by electrophoretic mobility shift assay. Ectopic expression of KLF4 decreases the mRNA and protein levels of survivin. Furthermore, overexpression of survivin partially reverses KLF4-induced cell apoptosis. These results indicate that KLF4 is a transcriptional repressor of the human survivin gene in esophageal squamous cancer cells.
在癌细胞中,survivin的异常表达已被证明在转录水平受到调控。在本研究中,我们证明在人类survivin基因转录起始位点上游2000 bp区域内存在六个假定的Krüppel样因子4(KLF4)结合位点。荧光素酶报告基因检测显示,在EC9706细胞中过表达KLF4时,survivin启动子活性受到抑制。染色质免疫沉淀检测表明,KLF4在体内确实与survivin启动子结合。通过电泳迁移率变动分析确定,它特异性结合六个结合位点中位于-40位置的位点。KLF4的异位表达降低了survivin的mRNA和蛋白质水平。此外,survivin的过表达部分逆转了KLF4诱导的细胞凋亡。这些结果表明,KLF4是食管鳞状癌细胞中人类survivin基因的转录抑制因子。