HCSGD entry for SOX1


1. General information

Official gene symbolSOX1
Entrez ID6656
Gene full nameSRY (sex determining region Y)-box 1
Other gene symbols
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:0001046Core promoter sequence-specific DNA bindingIDAmolecular_function
GO:0001764Neuron migrationIEAbiological_process
GO:0002089Lens morphogenesis in camera-type eyeIEAbiological_process
GO:0003677DNA bindingNASmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityNASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusNAScellular_component
GO:0006325Chromatin organizationNASbiological_process
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedNASbiological_process
GO:0021521Ventral spinal cord interneuron specificationIEAbiological_process
GO:0021884Forebrain neuron developmentIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.56632062230.88316537750.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.0198136602
GSE13712_SHEARDown-0.1622630344
GSE13712_STATICDown-0.0978821447
GSE19018Up0.1281920659
GSE19899_A1Down-0.0412005088
GSE19899_A2Up0.1138415353
PubMed_21979375_A1Up0.0797036065
PubMed_21979375_A2Down-0.0470125362
GSE35957Up0.1037149489
GSE36640Up0.0520656056
GSE54402Up0.0442561119
GSE9593Up0.0244600145
GSE43922Up0.1490117766
GSE24585Up0.0341147802
GSE37065Down-0.0807219806
GSE28863_A1Down-0.0589473457
GSE28863_A2Down-0.0103618797
GSE28863_A3Up0.5764366057
GSE28863_A4Down-0.0423773662
GSE48662Up0.0467221754

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-335-5pMIMAT0000765MIRT017005MicroarrayFunctional MTI (Weak)18185580
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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

25427424SOX1 down-regulates beta-catenin and reverses malignant phenotype in nasopharyngeal carcinoma
25427424Previous studies have demonstrated that the developmental gene sex-determining region Y (SRY)-box 1 (SOX1) inhibits cervical and liver tumorigenesis by interfering with the Wnt/beta-catenin signaling pathway
25427424However, the role of SOX1 in NPC remains unclear
25427424This study investigates the function of SOX1 in NPC pathogenesis
25427424RESULTS: Down-regulation of SOX1 was detected in NPC cell lines and tissues
25427424Besides, quantitative methylation-specific polymerase chain reaction revealed that SOX1 promoter was hypermethylated in NPC cell lines
25427424Ectopic expression of SOX1 in NPC cells suppressed colony formation, proliferation and migration in vitro and impaired tumor growth in nude mice
25427424Restoration of SOX1 expression significantly reduced epithelial-mesenchymal transition, enhanced cell differentiation and induced cellular senescence
25427424Conversely, transient knockdown of SOX1 by siRNA in these cells partially restored cell proliferation and colony formation
25427424Notably, SOX1 was found to physically interact with beta-catenin and reduce its expression independent of proteasomal activity, leading to inhibition of Wnt/beta-catenin signaling and decreased expression of downstream target genes
25427424CONCLUSIONS: SOX1 decreases the expression of beta-catenin in a proteasome-independent manner and reverses the malignant phenotype in NPC cells
22767186SOX1 functions as a tumor suppressor by antagonizing the WNT/beta-catenin signaling pathway in hepatocellular carcinoma
22767186SOX1 encodes a transcription factor involved in the regulation of embryonic development and cell fate determination
22767186In this study, we confirmed via quantitative methylation-specific polymerase chain reaction that SOX1 was frequently downregulated through promoter hypermethylation in HCC cells and tissues
22767186Overexpression of SOX1 by a constitutive or inducible approach could suppress cell proliferation, colony formation, and invasion ability in HCC cell lines, as well as tumor growth in nonobese diabetic/severe combined immunodeficiency mice
22767186We used a T cell factor (TCF)-responsive luciferase reporter assay and western blot analysis to prove that SOX1 could regulate TCF-responsive transcriptional activity and inhibit the expression of Wnt downstream genes
22767186Furthermore, we used glutathione S-transferase pull-down, co-immunoprecipitation, and confocal microscopy to demonstrate that SOX1 could interact with beta-catenin but not with the beta-catenin/TCF complex
22767186Moreover, restoration of the expression of SOX1 induces significant cellular senescence in Hep3B cells
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