HCSGD entry for CDC25A


1. General information

Official gene symbolCDC25A
Entrez ID993
Gene full namecell division cycle 25A
Other gene symbolsCDC25A2
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:0000079Regulation of cyclin-dependent protein serine/threonine kinase activityTASbiological_process
GO:0000082G1/S transition of mitotic cell cycleTASbiological_process
GO:0000086G2/M transition of mitotic cell cycleTASbiological_process
GO:0000278Mitotic cell cycleTASbiological_process
GO:0004725Protein tyrosine phosphatase activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005622IntracellularIEAcellular_component
GO:0005634NucleusIEAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005737CytoplasmIEAcellular_component
GO:0005829CytosolTAScellular_component
GO:0006260DNA replicationTASbiological_process
GO:0007067MitosisIEAbiological_process
GO:0008283Cell proliferationTASbiological_process
GO:0009314Response to radiationIDAbiological_process
GO:0019901Protein kinase bindingIPImolecular_function
GO:0034644Cellular response to UVIDAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.96556104250.00673900310.99999024730.1645429499

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

Data sourceUp or downLog fold change
GSE11954Down-0.2371958244
GSE13712_SHEARUp0.4364709989
GSE13712_STATICUp0.3412879252
GSE19018Down-0.5864995406
GSE19899_A1Down-0.3148212019
GSE19899_A2Down-1.4199986165
PubMed_21979375_A1Down-0.4415653819
PubMed_21979375_A2Down-1.9697641194
GSE35957Down-0.8002236381
GSE36640Down-2.6907805515
GSE54402Down-0.0760448687
GSE9593Down-0.4527357496
GSE43922Down-0.0238804612
GSE24585Up0.0870354311
GSE37065Down-0.2134385509
GSE28863_A1Down-0.1022342831
GSE28863_A2Up0.3027797164
GSE28863_A3Up0.0479477528
GSE28863_A4Up0.0264778620
GSE48662Down-0.7829167869

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-21-5pMIMAT0000076MIRT000157Microarray//Northern blot//qRT-PCRFunctional MTI (Weak)19826040
hsa-miR-21-5pMIMAT0000076MIRT000157Luciferase reporter assayFunctional MTI23496142
hsa-miR-21-5pMIMAT0000076MIRT000157MicroarrayFunctional MTI (Weak)18591254
hsa-miR-15a-5pMIMAT0000068MIRT000284Luciferase reporter assayFunctional MTI18949056
hsa-miR-503-5pMIMAT0002874MIRT000648Luciferase reporter assayFunctional MTI19956200
hsa-miR-424-5pMIMAT0001341MIRT000655Luciferase reporter assayFunctional MTI19956200
hsa-miR-34a-5pMIMAT0000255MIRT001011Western blotNon-Functional MTI18406353
hsa-let-7b-5pMIMAT0000063MIRT002296Immunohistochemistry//qRT-PCRFunctional MTI (Weak)19966857
hsa-let-7b-5pMIMAT0000063MIRT002296Luciferase reporter assay//Microarray//Western blotFunctional MTI17699775
hsa-miR-449aMIMAT0001541MIRT003186Luciferase reporter assay//Microarray//qRT-PCR//Western blot//Reporter assay;Western blot;OtherFunctional MTI19833767
hsa-miR-449b-5pMIMAT0003327MIRT016138Reporter assay;Western blotFunctional MTI19833767
hsa-miR-193b-3pMIMAT0002819MIRT016313MicroarrayFunctional MTI (Weak)20304954
hsa-miR-192-5pMIMAT0000222MIRT026127MicroarrayFunctional MTI (Weak)19074876
hsa-miR-103a-3pMIMAT0000101MIRT027018SequencingFunctional MTI (Weak)20371350
hsa-miR-98-5pMIMAT0000096MIRT027421MicroarrayFunctional MTI (Weak)19088304
hsa-miR-16-5pMIMAT0000069MIRT031451SequencingFunctional MTI (Weak)20371350
hsa-miR-877-3pMIMAT0004950MIRT036976CLASHFunctional MTI (Weak)23622248
hsa-miR-18a-3pMIMAT0002891MIRT040942CLASHFunctional MTI (Weak)23622248
hsa-miR-484MIMAT0002174MIRT041718CLASHFunctional MTI (Weak)23622248
hsa-let-7i-5pMIMAT0000415MIRT046546CLASHFunctional MTI (Weak)23622248
hsa-miR-92a-3pMIMAT0000092MIRT049120CLASHFunctional MTI (Weak)23622248
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  • mirRecord

MicroRNA name

mirBase ID

Target site number

MiRNA mature ID

Test method inter

MiRNA regulation site

Reporter target site

Pubmed ID

hsa-let-7b-5pMIMAT0000063NAhsa-let-7b18026111
hsa-let-7b-5pMIMAT0000063NAhsa-let-7b{Western blot}{overexpression by miRNA precursor transfection}17699775
hsa-miR-125b-5pMIMAT0000423NAhsa-miR-125b{Western blot}{overexpression}19948152
hsa-miR-21-5pMIMAT00000761hsa-miR-21{Western blot}{knock out}19826040
hsa-miR-503-5pMIMAT00028741hsa-miR-503{Western blot}{overexpression by miRNA precursor transfection}21220732
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 3 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

23496142These two cell-cycle regulators are indirectly regulated by miR-21 via its validated direct targets NFIB (Nuclear factor 1 B-type), a transcriptional inhibitor of p21(CIP) (1) , and CDC25A, which regulates CDK2 activity by dephosphorylation
23496142Knock-down of either NFIB or CDC25A shows a phenocopy of over-expressing miR-21 in regard to cell-cycle arrest
23276696This effect was accompanied by the increased expression of cyclin E and CDC25A and the significantly decreased expression of cyclin-dependent kinase inhibitors
11103932Reduction of Cdc25A contributes to cyclin E1-Cdk2 inhibition at senescence in human mammary epithelial cells
11103932The inhibition of cyclin E-cdk2 in senescent HMECs was accompanied by increased inhibitory phosphorylation of cdk2, in association with a progressive loss of Cdc25A
11103932Recombinant Cdc25A strongly reactivated cyclin E-cdk2 from senescent HMECs suggesting that reduction of Cdc25A contributes to cyclin E-cdk2 inhibition and G1 arrest at senescence
11103932Although ectopic expression of Cdc25A failed to extend the lifespan of HMECs, the exogenous Cdc25A appeared to lack activity in these cells, since it neither shortened the G1-to-S phase interval nor activated cyclin E-cdk2
11103932In contrast, in the breast cancer-derived MCF-7 line, Cdc25A overexpression increased both cyclin E-cdk2 activity and the S phase fraction
11103932Thus, mechanisms leading to HMEC immortalization may involve not only the re-induction of Cdc25A expression, but also activation of this phosphatase
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