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Series GSE4427 Query DataSets for GSE4427
Status Public on Mar 12, 2006
Title Methylation induced by the RAS oncogene
Organism Rattus norvegicus
Experiment type Expression profiling by array
Summary Silencing of gene expression by methylation of CpG islands in regulatory elements is frequently observed in cancer. However, an influence of the most common oncogenic signalling pathways onto DNA methylation has not yet been investigated thoroughly. To address this issue, we identified genes suppressed in HRAS-transformed rat fibroblasts but up-regulated after treatment with the demethylating agent 5-Aza-CdR and with the MEK1,2 inhibitor U0126. Analysis of gene expression by microarray and Northern blot analysis revealed the MEK/ERK target genes clusterin, Mmp2, Ppicap, syndecan 4, Timp2, Thbs1 to be repressed in the HRAS-transformed FE-8 cells in a MEK/ERK- and in a methylation-dependent manner. Hypermethylation of putative regulatory elements in HRAS-transformed cells as compared to immortalized fibroblasts was detected within a CpG island 14.5 kb upstream of clusterin, within the clusterin promoter and within a CpG island of the Mmp2 promoter by bisulphite sequencing. Furthermore, hypermethylation of the clusterin promoter was observed ten days after induction of HRAS in immortalized rat fibroblasts and a clear correlation between reduced clusterin expression and hypermethlyation could also be observed in distinct rat tissues. These results suggest that silencing of individual genes by DNA methylation is controlled by oncogenic signalling pathways, yet the mechanisms responsible for initial target gene suppression are variable.
Keywords: expression analysis
 
Overall design Gene expression was analyzed in immortal (208F) and HRAS oncogene-transformed (FE8) rat fibroblasts after demethylation by 5-aza-2'-deoxycytidine. Genes potentially methylated in RAS-transformed cells were identified by bisulphite sequencing
 
Citation(s) 16568090
Submission date Mar 09, 2006
Last update date Feb 21, 2017
Contact name Christine Sers
E-mail(s) christine.sers@charite.de
Organization name Charite
Department Institute of Pathology
Street address Schumannstr. 20/21
City Berlin
ZIP/Postal code 10117
Country Germany
 
Platforms (1)
GPL85 [RG_U34A] Affymetrix Rat Genome U34 Array
Samples (6)
GSM99621 208F control
GSM99622 208F aza replicate 1
GSM99623 208F aza replicate 2
Relations
BioProject PRJNA94623

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Supplementary file Size Download File type/resource
GSE4427_RAW.tar 195.6 Mb (http)(custom) TAR (of DAT, EXP)

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