HCSGD entry for HOPX


1. General information

Official gene symbolHOPX
Entrez ID84525
Gene full nameHOP homeobox
Other gene symbolsCAMEO HOD HOP LAGY NECC1 OB1 SMAP31 TOTO
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:0000122Negative regulation of transcription from RNA polymerase II promoterIEAbiological_process
GO:0001829Trophectodermal cell differentiationIDA IEAbiological_process
GO:0003677DNA bindingIEAmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIEAmolecular_function
GO:0005634NucleusIDA IEAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0007507Heart developmentIEAbiological_process
GO:0008016Regulation of heart contractionIEAbiological_process
GO:0016575Histone deacetylationIEAbiological_process
GO:0043393Regulation of protein bindingIEAbiological_process
GO:0043415Positive regulation of skeletal muscle tissue regenerationIEAbiological_process
GO:0043565Sequence-specific DNA bindingIEAmolecular_function
GO:0045596Negative regulation of cell differentiationIDAbiological_process
GO:0048286Lung alveolus developmentIEAbiological_process
GO:0051155Positive regulation of striated muscle cell differentiationIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.24179232930.61597531630.92885404701.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.0432362038
GSE13712_SHEARUp0.5380323532
GSE13712_STATICUp0.3281510624
GSE19018Down-0.0059805420
GSE19899_A1Up0.0807491666
GSE19899_A2Down-0.6654694998
PubMed_21979375_A1Down-0.1300375337
PubMed_21979375_A2Up0.1841514693
GSE35957Down-0.0921755053
GSE36640Up0.6040925973
GSE54402Down-0.2807951148
GSE9593Up0.0366690609
GSE43922Up0.0230777100
GSE24585Down-0.2262618629
GSE37065Down-0.0262112835
GSE28863_A1Up0.0469026524
GSE28863_A2Up0.0802773043
GSE28863_A3Up0.1854010993
GSE28863_A4Down-0.0664547099
GSE48662Up0.4340898167

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase
No target information from mirTarBase
    • 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

25345926HOPX is methylated and exerts tumour-suppressive function through Ras-induced senescence in human lung cancer
25345926HOPX acts as a tumour suppressor in various cancers
25345926However, the regulation of HOPX in human lung cancer as well as the mechanism underlying its tumour-suppressive function has not yet been well elucidated
25345926Here we investigated the epigenetic regulation and molecular mechanism by which HOPX exerts growth inhibitory effects
25345926We found that HOPX was down-regulated in 12 out of 13 lung cancer cell lines and in 69 out of 120 primary lung tumours at mRNA and protein levels
25345926Patients with lung adenocarcinoma (ADC) exhibited significantly more positive staining of HOPX protein compared with lung squamous cell carcinoma (SCC) (p =0
25345926Again in ADC, patients with higher HOPX expression had a significantly longer disease-free survival (p =0
25345926Methylation analysis showed that down-regulation of HOPX was associated with DNA methylation (p =0
25345926To analyse the function of HOPX in lung cancer cells, stable transfection with an expression vector of HOPX was performed
25345926It turned out that HOPX inhibited tumour cell proliferation rate, migration, and invasion, and, more interestingly, forced expression of HOPX enhanced cellular senescence via activation of oncogenic Ras and the downstream MAPK pathway, which in turn led to decreased MDM2 and increased p21
25345926On the contrary, knockdown of HOPX by siRNA resulted in reduced Ras activity, inactivation of the MAPK pathway, and decreased p21 levels, accompanied by reduced cellular senescence
25345926Taken together, our data suggest that down-regulation of HOPX was related to DNA methylation and that HOPX exerts tumour-suppressive activity by oncogenic Ras-induced cellular senescence in lung cancer cells
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