Ma Juan, Mi Chunliu, Wang Ke Si, Lee Jung Joon, Jin Xuejun
Key Laboratory of Natural Resources of Changbai Mountain & Functional Molecules, Ministry of Education, Molecular Medicine Research Center, College of Pharmacy, Yanbian University, Yanji 133002, Jilin Province, China.
Oncotarget. 2016 Jun 14;7(24):36551-36562. doi: 10.18632/oncotarget.9070.
Zinc finger protein 91 (ZFP91) has been reported to be involved in various biological processes. However, the clinical significance and biological role of ZFP91 in colon cancer remains unknown. Here, we show that ZFP91 expression is upregulated in patients with colon cancer. We found that ZFP91 upregulated HIF-1α at the levels of promoter and protein in colon cancer cells. Using chromatin immunoprecipitation, electrophoretic mobility shift assay and luciferase reporter gene assay, we found that NF-κB/p65 is required for the binding of ZFP91 to the HIF-1α promoter at -197/-188 base pairs and for the transcriptional activation of HIF-1α gene mediated by ZFP91. Flow cytometry, 5-ethynyl-2'-deoxyuridine (EdU) incorporation and tumor xenograft assay demonstrated that ZFP91 enhanced cell proliferation of colon cancer through upregulating HIF-1α in vitro and in vivo. Furthermore, ZFP91 is positively associated with HIF-1α in human colon cancer. Thus, we concluded that ZFP91 activates transcriptional coregulatory protein HIF-1α through transcription factor NF-κB/p65 in the promotion of proliferation and tumorigenesis in colon cancer cell. ZFP91 may serve as a driver gene to activate HIF-1α transcription in the development of cancer.
据报道,锌指蛋白91(ZFP91)参与多种生物学过程。然而,ZFP91在结肠癌中的临床意义和生物学作用仍不清楚。在此,我们表明ZFP91在结肠癌患者中表达上调。我们发现ZFP91在启动子和蛋白质水平上上调结肠癌细胞中的缺氧诱导因子-1α(HIF-1α)。通过染色质免疫沉淀、电泳迁移率变动分析和荧光素酶报告基因分析,我们发现核因子κB/p65(NF-κB/p65)是ZFP91与HIF-1α启动子在-197/-188碱基对处结合以及ZFP91介导的HIF-1α基因转录激活所必需的。流式细胞术、5-乙炔基-2'-脱氧尿苷(EdU)掺入和肿瘤异种移植试验表明,ZFP91在体外和体内通过上调HIF-1α增强结肠癌细胞的增殖。此外,在人类结肠癌中,ZFP91与HIF-1α呈正相关。因此,我们得出结论,ZFP91通过转录因子NF-κB/p65激活转录共调节蛋白HIF-1α,促进结肠癌细胞的增殖和肿瘤发生。ZFP91可能作为驱动基因在癌症发生发展过程中激活HIF-1α转录。