Literature DB >> 23872552

Transcriptional regulation of the growth-regulated oncogene α gene by early growth response protein-1 in response to tumor necrosis factor α stimulation.

Soon Young Shin1, Jong Min Lee, Yoongho Lim, Young Han Lee.   

Abstract

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.
© 2013.

Entities:  

Keywords:  ChIP; Chromatin immunoprecipitation; EBS; EMSA; Egr-1; Egr-1-binding sequence; Electrophoretic mobility shift assay; GROα; Growth-regulated oncogene α; IL; Interleukin; MAPK; Mitogen-activated protein kinase; RT-PCR; Reverse transcription-polymerase chain reaction; TNFα; Transcriptional regulation; Tumor microenvironment; Tumor necrosis factor α; siRNA; small-interfering RNA

Mesh:

Substances:

Year:  2013        PMID: 23872552     DOI: 10.1016/j.bbagrm.2013.07.005

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


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