Shin Soon Young, Lee Jong Min, Lim Yoongho, Lee Young Han
Department of Biological Sciences, College of Biological Science and Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea; Cancer and Metabolism Institute, Konkuk University, Seoul 143-701, Republic of Korea.
Biochim Biophys Acta. 2013 Oct;1829(10):1066-74. doi: 10.1016/j.bbagrm.2013.07.005. Epub 2013 Jul 18.
Growth-regulated oncogene α (GROα) plays an important role in a wide range of normal and pathological conditions, including inflammation, angiogenesis, wound healing, tumor invasion, and metastasis. Egr-1 is a member of the zinc-finger transcription factor family induced by diverse stimuli, including TNFα. However, the role of Egr-1 in GROα expression was previously unknown. This study shows that Egr-1 directly binds to the GROα promoter and transactivates the GROα gene. Silencing of Egr-1 by expression of Egr-1 siRNA abrogated TNFα-induced GROα transcription. We also found that Egr-1 mediates ERK and JNK MAPK-dependent GROα transcription upon TNFα stimulation. Our findings suggest that Egr-1 may play an important role in tumor development through transactivation of the GROα gene in response to TNFα within the tumor microenvironment.
生长调节致癌基因α(GROα)在广泛的正常和病理状况中发挥重要作用,包括炎症、血管生成、伤口愈合、肿瘤侵袭和转移。Egr-1是锌指转录因子家族的成员,可由多种刺激诱导产生,包括肿瘤坏死因子α(TNFα)。然而,Egr-1在GROα表达中的作用此前尚不清楚。本研究表明,Egr-1直接结合GROα启动子并反式激活GROα基因。通过表达Egr-1小干扰RNA(siRNA)使Egr-1沉默可消除TNFα诱导的GROα转录。我们还发现,在TNFα刺激下,Egr-1介导细胞外信号调节激酶(ERK)和应激活化蛋白激酶(JNK)丝裂原活化蛋白激酶(MAPK)依赖性的GROα转录。我们的研究结果表明,Egr-1可能通过在肿瘤微环境中响应TNFα反式激活GROα基因,在肿瘤发展中发挥重要作用。