Adamson Eileen, de Belle Ian, Mittal Shalu, Wang Yipeng, Hayakawa Jun, Korkmaz Kemal, O'Hagan David, McClelland Michael, Mercola Dan
The Burnham Institute, Cancer Research Center, La Jolla, California 92037, USA.
Cancer Biol Ther. 2003 Nov-Dec;2(6):617-22.
Egr1 is a multifunctional transcription factor regulating a remarkable spectrum of cellular responses from survival to apoptosis, growth to growth arrest, differentiation to transformation, senescence as well as memory and learning effects. In prostate cancer, Egr1 levels are constitutively high and closely linked to cancer development and progression. This zinc-finger protein is a short-lived, immediate early growth response gene known to be induced by a large number of extracellular stimuli such as irradiation (all wavelengths tested), hypoxia, hyperoxia, chemotherapy agents, and more. Therefore the target genes that Egr1 regulates in prostate cancer cells play an important role in generating many of the cellular responses that characterize these cells. After Egr1 binds to its binding sites on gene promoters, specificity of response is determined by whether Egr1 transcriptionally up- or downregulates the target genes. Expression microarray analyses combined with binding data promise new ways to identify stage specific cancer markers, to aid in patient risk assessment and in therapeutic choices.
Egr1是一种多功能转录因子,可调节从存活到凋亡、生长到生长停滞、分化到转化、衰老以及记忆和学习效应等一系列显著的细胞反应。在前列腺癌中,Egr1水平持续较高,且与癌症的发生和进展密切相关。这种锌指蛋白是一种寿命较短的即时早期生长反应基因,已知可被大量细胞外刺激诱导,如辐射(所有测试波长)、缺氧、高氧、化疗药物等。因此,Egr1在前列腺癌细胞中调节的靶基因在产生这些细胞特有的许多细胞反应中起重要作用。Egr1与其在基因启动子上的结合位点结合后,反应的特异性取决于Egr1是转录上调还是下调靶基因。表达微阵列分析与结合数据相结合,有望为识别阶段特异性癌症标志物、辅助患者风险评估和治疗选择提供新方法。