HCSGD entry for EHF


1. General information

Official gene symbolEHF
Entrez ID26298
Gene full nameets homologous factor
Other gene symbolsESE3 ESE3B ESEJ
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0003677DNA bindingIDA TASmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIDAmolecular_function
GO:0005634NucleusIC IEAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0007275Multicellular organismal developmentTASbiological_process
GO:0008283Cell proliferationTASbiological_process
GO:0030855Epithelial cell differentiationIEPbiological_process
GO:0043565Sequence-specific DNA bindingIEAmolecular_function
GO:0045893Positive regulation of transcription, DNA-templatedIDAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00006744420.99467669160.02247088611.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up1.2717115462
GSE13712_SHEARDown-0.0705960555
GSE13712_STATICDown-0.1049808761
GSE19018Up0.1563475863
GSE19899_A1Up1.5343696640
GSE19899_A2Up4.2308997429
PubMed_21979375_A1Up5.5243531456
PubMed_21979375_A2Up3.3985664265
GSE35957Up0.6398910176
GSE36640Up1.7929388043
GSE54402Up4.4873155705
GSE9593Up0.0287093699
GSE43922Up5.0885147819
GSE24585Up0.1067490114
GSE37065Up0.2408540503
GSE28863_A1Down-0.0585169081
GSE28863_A2Up0.0570770094
GSE28863_A3Up0.0958923401
GSE28863_A4Up0.0324096824
GSE48662Down-0.0220607291

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-335-5pMIMAT0000765MIRT017515MicroarrayFunctional MTI (Weak)18185580
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  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

17627613ESE-3, an Ets family transcription factor, is up-regulated in cellular senescence
17627613It was found that five genes encoding ESE-3, inhibin betaA, RGS5, SSAT and DIO2 were up-regulated in senescent cells induced by RasV12, H(2)O(2) and telomere shortening, but not in quiescent or actively growing cells, suggesting that these genes serve as molecular markers for various types of cellular senescence
17627613The ectopic expression of ESE-3 resulted in retarded growth, up-regulation of p16(INK4a) but not of p21, and increased levels of SA-beta-gal activity
17627613ESE-3 expression increased the activity of the p16(INK4a) promoter in a reporter assay, and recombinant ESE-3 protein bound to the Ets-binding sequences present in the promoter
17172423Influence of small interfering RNA corresponding to ets homologous factor on senescence-associated modulation of prostate carcinogenesis
17172423In the process of identifying senescence-associated genes, we found significant suppression of the ets homologous factor (EHF) in cancer cells in a state of DNA damage-induced senescence
17172423In this study, we show that EHF provides substantial drug resistance in PC-3 prostate cancer cells by inhibiting senescence and cell cycle arrest
17172423Telomeric repeat amplification protocol analysis showed that transient EHF knockdown significantly decreased telomerase activity, whereas this activity was increased by overexpression of EHF
17172423Further, the preestablished tumors were reduced after the injection of small interfering RNA corresponding to EHF (P = 0
17172423Collectively, these observations indicate that aberrant expression of EHF and the subsequent disruption of p27-mediated senescence and telomerase activity is likely to contribute significantly to tumor progression, and furthermore that EHF might be a promising target for future cancer therapeutics
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