HCSGD entry for NINJ1


1. General information

Official gene symbolNINJ1
Entrez ID4814
Gene full nameninjurin 1
Other gene symbolsNIN1 NINJURIN
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:0007155Cell adhesionIEAbiological_process
GO:0007399Nervous system developmentTASbiological_process
GO:0016021Integral component of membraneIEAcellular_component
GO:0042246Tissue regenerationIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00266375520.89414124460.13915059291.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.9111795973
GSE13712_SHEARUp0.2788712532
GSE13712_STATICUp0.5956509212
GSE19018Down-0.1952127988
GSE19899_A1Up0.1911409997
GSE19899_A2Up2.0770406503
PubMed_21979375_A1Up1.6889248866
PubMed_21979375_A2Up2.7173357274
GSE35957Down-0.7843878107
GSE36640Up0.4544021902
GSE54402Up1.1135704190
GSE9593Down-0.1840651478
GSE43922Up0.4998492493
GSE24585Up0.1412926018
GSE37065Up0.5885060865
GSE28863_A1Up0.0382103539
GSE28863_A2Down-0.4416300678
GSE28863_A3Down-0.1575172095
GSE28863_A4Down-0.0261123013
GSE48662Up0.2446289350

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-107MIMAT0000104MIRT026972MicroarrayFunctional MTI (Weak)20489155
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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

23690620Ninjurin1, a target of p53, regulates p53 expression and p53-dependent cell survival, senescence, and radiation-induced mortality
23690620The nerve injury-induced protein 1 (Ninjurin1, Ninj1) is a homophilic adhesion molecule and involved in nerve regeneration
23690620Interestingly, Ninj1 is found to be overexpressed in human cancer, but its role in tumorigenesis is not clear
23690620Here, we found that Ninj1 is transcriptionally regulated by p53 and can be induced by DNA damage in a p53-dependent manner
23690620We also found that knockout or knockdown of Ninj1 increases p53 expression potentially through enhanced p53 mRNA translation
23690620In addition, we found that Ninj1 deficiency suppresses cell proliferation but enhances apoptosis and premature senescence in a p53-dependent manner
23690620Taken together, we provided evidence that Ninj1 is a p53 target and modulates p53 mRNA translation and p53-dependent premature senescence, cell proliferation, apoptosis, and radiation-induced mortality in vitro and in vivo
23690620Thus, we postulate that as a membrane adhesion molecule, Ninj1 is an ideal target to regulate p53 activity via the p53-Ninj1 loop
15464245Ninjurin1 increases p21 expression and induces cellular senescence in human hepatoma cells
15464245BACKGROUND/AIMS: Ninjurin1 is a novel adhesion molecule that has a role in promoting nerve regeneration
15464245Although ninjurin1 is ubiquitously expressed in various human tissues, including the liver, the biologic functions of ninjurin1 in tissues other than the nervous system remain unknown
15464245The aim of this study was to investigate the function of ninjurin1 in hepatocytes
15464245METHODS: The effect of ninjurin1 overexpression was examined in Huh-7 hepatoma cells
15464245Ninjurin1 expression was examined by Western blot in human hepatocellular carcinoma tissues as well as their adjacent liver tissues
15464245The levels of ninjurin1 expression were higher in hepatocellular carcinoma tissues than those in adjacent liver tissues
15464245CONCLUSIONS: The present study provides the first evidence that ninjurin1 is able to induce the senescence program
15464245Ninjurin1 may be involved in the regulation of cellular senescence in the liver during carcinogenesis
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