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Series GSE40558 Query DataSets for GSE40558
Status Public on Apr 01, 2013
Title Involvement of transcription factor early growth response 4 (EGR4) in lung cancer bone metastasis
Organism Homo sapiens
Experiment type Expression profiling by array
Summary EGR4 (early growth response 4), a transcription factor, was previously shown to be up-regulated in lung cancer bone metastasis, compared with its expression in metastasis in other organs, using a multiorgan metastasis model of human small-cell lung cancer cells (SBC-5) in NK cell-depleted SCID mice (Kakiuchi S et al. Mol Cancer Res 2003). Here we show that EGR4 was essential for survival cancer cells, and migration ability. Next, in searching of downstream genes regulated by EGR4, we analyzed the changes in transcriptomes of SBC-5 cells at different time-points (24, 48 and 72 hr) when knockdown of EGR4 by siRNA. Lots of genes were identified either up-regulated or down-regulated in siEGR4 samples compared with control siRNA. Among these genes, there were genes with roles in metastasis or bone biology. The fact that EGR4 knockdown led to up-regulation or suppression of these genes also indicated dual roles of EGR4 in transcriptional regulation, which is consistent with previous reports: EGR4 may repress its own promoter (Zipfel PF et al. Biochim Biophys Acta. 1997) or activate certain inflammatory genes (Decker EL et al. Nucleic Acids Res. 2003; Wieland GD et al. J Cell Sci. 2005).
 
Overall design SBC-5 cells were cultured at 1x10^6 cells/2 ml in 3.5 cm plate. After seeding 24 hours, cells were transfected either siEGR4 or siEGFP (for control), using Lipofectamin. At 24, 48 and 72 hours after starting of siRNA, we extracted RNA from these cells, and subjected these RNAs to microarray analysis. The labeling, amplification, hybridization and microarray data analysis were described previously (Dat LT et al. Int J Oncol, 40: 1455-1469 2012).
 
Contributor(s) Dat LT, Matsuo T, Yoshimaru T, Kuramoto T, Hanibuchi M, Goto H, Kakiuchi S, Mitsuhashi A, Nishioka Y, Sone S, Katagiri T
Citation(s) 25411851
Submission date Sep 03, 2012
Last update date Mar 26, 2020
Contact name Le Tan Dat
E-mail(s) letandat@genome.tokushima-u.ac.jp
Phone +81-90-1327-6064
Fax 088-633-7122
URL http://www.genome.tokushima-u.ac.jp/dgm/
Organization name Tokushima university
Department Genome center
Lab Genome medicine
Street address 3-18-15, Kuramoto-cho
City Tokushima
State/province Tokushima
ZIP/Postal code 770-8503
Country Japan
 
Platforms (1)
GPL6480 Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Probe Name version)
Samples (14)
GSM996503 SBC-5 (0)_1
GSM996504 SBC-5 (0)_2
GSM996505 siEGFP (24 hr) _1
Relations
BioProject PRJNA174294

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE40558_RAW.tar 30.5 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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