HCSGD entry for DUSP16


1. General information

Official gene symbolDUSP16
Entrez ID80824
Gene full namedual specificity phosphatase 16
Other gene symbolsMKP-7 MKP7
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:0000188Inactivation of MAPK activityIBA IEA TASbiological_process
GO:0004721Phosphoprotein phosphatase activityTASmolecular_function
GO:0004725Protein tyrosine phosphatase activityIEAmolecular_function
GO:0005634NucleusIBA IEA TAScellular_component
GO:0005737CytoplasmIBA IEA TAScellular_component
GO:0006470Protein dephosphorylationIBAbiological_process
GO:0016023Cytoplasmic membrane-bounded vesicleIEAcellular_component
GO:0016311DephosphorylationTASbiological_process
GO:0016791Phosphatase activityIEAmolecular_function
GO:0017017MAP kinase tyrosine/serine/threonine phosphatase activityIBAmolecular_function
GO:0045204MAPK export from nucleusTASbiological_process
GO:0045209MAPK phosphatase export from nucleus, leptomycin B sensitiveTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00467445390.98046005090.17987763161.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.0004061370
GSE13712_SHEARUp0.8293661609
GSE13712_STATICUp0.5142293623
GSE19018Down-0.0197426412
GSE19899_A1Up0.0977450138
GSE19899_A2Up1.2372899959
PubMed_21979375_A1Up1.3699679220
PubMed_21979375_A2Up1.1100932965
GSE35957Down-0.2504952953
GSE36640Down-0.2069367954
GSE54402Up0.7119124276
GSE9593Down-0.0690906086
GSE43922Up0.8019960950
GSE24585Up0.2238923791
GSE37065Up0.3473954640
GSE28863_A1Up1.1721233801
GSE28863_A2Up0.4197631916
GSE28863_A3Down-0.0344544552
GSE28863_A4Up0.0248031310
GSE48662Down-0.0977442625

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-335-5pMIMAT0000765MIRT016920MicroarrayFunctional MTI (Weak)18185580
hsa-miR-192-5pMIMAT0000222MIRT026190MicroarrayFunctional MTI (Weak)19074876
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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

26381291DUSP16 ablation arrests the cell cycle and induces cellular senescence
26381291In particular, we showed that DUSP16 ablation leads to a G1/S transition arrest, reduced incorporation of 5-bromodeoxyuridine, enhanced senescence-associated beta-galactosidase activity, and formation of senescence-associated heterochromatic foci
26381291Mechanistically, DUSP16 silencing causes cellular senescence by activating the tumor suppressors p53 and Rb
26381291The phosphatase activity of DUSP16 is necessary for antagonizing cellular senescence
26381291Importantly, the expression levels of DUSP16 are up-regulated in human liver cancers, and are positively correlated with tumor cell proliferation
26381291Taken together, our findings indicate that DUSP16 plays a role in tumorigenesis by protecting cancer cells from senescence
25077541We demonstrate that miR-17 targets both ADCY5 and IRS1, upregulating the downstream signals MKP7, FoxO3, LC3B, and HIF1alpha, and downregulating mTOR, c-myc, cyclin D1, and JNK
25077541Repression of ADCY5 by miR-17 translocated membrane-bound RGS2 into the nucleus, promoting interactions of RGS2 with HIF1alpha and the MKP7 promoter, enhancing MKP7 transcription
25077541ADCY5 repression by miR-17 also facilitated the translocation of EGFR and MKP7 from membrane into cytoplasmic and mitochondrial fractions
25077541Importantly, we found that MKP7 inhibited senescence by dephosphorylating PRAS40 at Thr246 and mTOR at Ser2248, facilitating the interaction and loss of function of both molecules
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