HCSGD entry for ENO1


1. General information

Official gene symbolENO1
Entrez ID2023
Gene full nameenolase 1, (alpha)
Other gene symbolsENO1L1 MPB1 NNE PPH
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000015Phosphopyruvate hydratase complexIEAcellular_component
GO:0000122Negative regulation of transcription from RNA polymerase II promoterTASbiological_process
GO:0000287Magnesium ion bindingIEAmolecular_function
GO:0003677DNA bindingIEAmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityTASmolecular_function
GO:0003714Transcription corepressor activityTASmolecular_function
GO:0004634Phosphopyruvate hydratase activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusICcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005829CytosolTAScellular_component
GO:0005886Plasma membraneIEAcellular_component
GO:0005975Carbohydrate metabolic processTASbiological_process
GO:0006006Glucose metabolic processTASbiological_process
GO:0006094GluconeogenesisTASbiological_process
GO:0006096GlycolysisIEA TASbiological_process
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0009615Response to virusIEPbiological_process
GO:0030308Negative regulation of cell growthIDAbiological_process
GO:0031430M bandIEAcellular_component
GO:0044281Small molecule metabolic processTASbiological_process
GO:0045892Negative regulation of transcription, DNA-templatedIDAbiological_process
GO:0070062Extracellular vesicular exosomeIDAcellular_component
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.63300755670.01729987080.99999024730.2574145845

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

Data sourceUp or downLog fold change
GSE11954Down-0.7136250378
GSE13712_SHEARUp0.4331065657
GSE13712_STATICUp0.3383148787
GSE19018Up0.8067848179
GSE19899_A1Down-0.0085325433
GSE19899_A2Down-0.2424597532
PubMed_21979375_A1Up0.6801663583
PubMed_21979375_A2Down-0.9956381857
GSE35957Down-0.3675975754
GSE36640Down-1.2428289474
GSE54402Down-0.3438091828
GSE9593Up0.0318219521
GSE43922Up0.0992852624
GSE24585Down-0.3156676706
GSE37065Down-0.1995672112
GSE28863_A1Down-0.3732451271
GSE28863_A2Down-0.5621689557
GSE28863_A3Down-0.0775687286
GSE28863_A4Down-0.3759693531
GSE48662Up0.1324182912

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-744-5pMIMAT0004945MIRT037729CLASHFunctional MTI (Weak)23622248
hsa-miR-615-3pMIMAT0003283MIRT039693CLASHFunctional MTI (Weak)23622248
hsa-miR-18a-3pMIMAT0002891MIRT040892CLASHFunctional MTI (Weak)23622248
hsa-miR-181d-5pMIMAT0002821MIRT041167CLASHFunctional MTI (Weak)23622248
hsa-miR-484MIMAT0002174MIRT041760CLASHFunctional MTI (Weak)23622248
hsa-miR-378a-3pMIMAT0000732MIRT043896CLASHFunctional MTI (Weak)23622248
hsa-miR-125a-5pMIMAT0000443MIRT045746CLASHFunctional MTI (Weak)23622248
hsa-miR-222-3pMIMAT0000279MIRT046821CLASHFunctional MTI (Weak)23622248
hsa-miR-204-5pMIMAT0000265MIRT047021CLASHFunctional MTI (Weak)23622248
hsa-miR-92a-3pMIMAT0000092MIRT049082CLASHFunctional MTI (Weak)23622248
hsa-miR-1260bMIMAT0015041MIRT052701CLASHFunctional MTI (Weak)23622248
hsa-miR-3177-3pMIMAT0015054MIRT052801CLASHFunctional MTI (Weak)23622248
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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: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26734996Targeting the Warburg effect in cancer cells through ENO1 knockdown rescues oxidative phosphorylation and induces growth arrest
26734996Alpha-enolase (ENO1) is commonly over-expressed in tumors and is a clinically relevant candidate molecular target for immunotherapy
26734996Here, we silenced ENO1 in human cancer cell lines and evaluated its impact through proteomic, biochemical and functional approaches
26734996ENO1 silencing increased reactive oxygen species that were mainly generated through the sorbitol and NADPH oxidase pathways, as well as autophagy and catabolic pathway adaptations, which together affect cancer cell growth and induce senescence
26734996These findings represent the first comprehensive metabolic analysis following ENO1 silencing
26734996Inhibition of ENO1, either alone, or in combination with other pathways which were perturbed by ENO1 silencing, opens novel avenues for future therapeutic approaches
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