SOX4 (SRY (sex determining region Y)-box 4)

2009-01-01   David L Satinover , Chris A Moskaluk 

Dept. of Pathology, Dept. of Biochemistry, Molecular Genetics P.O. Box 800214 University of Virginia Health System Charlottesville, VA 22908, USA

Identity

HGNC
LOCATION
6p22.3
LOCUSID
ALIAS
CSS10,EVI16
FUSION GENES

DNA/RNA

Description

This intronless gene encompasses 4789 base pairs.

Transcription

The mRNA transcript is 4789 base pairs.

Proteins

Description

The mRNA encodes a 47.3 kDa protein consisting of 474 amino acids.

Expression

SOX4 appears to be fairly ubiquitously expressed at low levels in most adult tissues, with high levels found mostly in T lymphocytes. Its expression is up-regulated in many cancer types relative to benign tissue of origin (Rhodes et al., 2004).

Localisation

Nucleus.

Function

SOX4 is a member of the class I SRY-related HMG-box family of transcription factors. It has been shown to be involved in determination of cell fate and the regulation of embryonic development of many organ systems including heart (Restivo et al., 2006; Schilham et al., 1996), pancreas (Lioubinski et al., 2003; Wilson et al., 2005) and brain (Cheung et al., 2000; Hong and Saint-Jeannet, 2005). SOX4 has been shown to be a transcriptional activator in lymphocytes (van de Wetering et al., 1993) and facilitates B and T cell differentiation (Schilham et al., 1996; Schilham et al., 1997). SOX4 gene expression is up-regulated in many tumor types, with experimental evidence suggesting that this contributes to cellular transformation (Liu et al., 2006; Shin et al., 2004), control of apoptosis (Liu et al., 2006; Pramoonjago et al., 2006; Aaboe et al., 2006; Ahn et al., 2002) and/or a metastatic phenotype (Liao et al., 2008; Tavazoie et al., 2008).

Homology

SOX4 is part of a family of Sox transcription factors that share significant homology. SOX4 is in the Group C Sox homology group that includes SOX11, SOX22 and SOX24. SOX4 shares the highest degree of homology with SOX11 (Bowles et al., 2000).

Implicated in

Entity name
Adenoid Cystic Carcinoma (ACC)
Note
Gene expression profiling using micro arrays has shown SOX4 is one of the most up-regulated genes in ACC, relative to non-neoplastic tissue of origin (Frierson et al., 2002). Immunohistochemistry analysis confirms the up-regulation of SOX4 in primary ACC tumors compared to normal tissue (Pramoonjago et al., 2006).
Disease
ACC is the second most common malignant salivary gland tumor, representing 28% of malignant submandibular gland tumors.
Entity name
Bladder Cancer
Note
Whole genome expression profiling of 166 bladder tumors and 27 normal samples showed SOX4 up-regulated 5 fold in the tumors. When over-expressed in the bladder cell line HU609, SOX4 strongly impaired cell viability and promoted apoptosis (Aaboe et al., 2006).
Prognosis
A correlation was found between strong SOX4 expression levels and increased patient survival.
Entity name
Breast Cancer
Note
MicroRNA miR335 has been shown to regulate Sox4 levels and is frequently found lost in primary tumors of breast cancer patients who relapse (Tavazoie et al., 2008). In experimental model systems, it appears that SOX4 is a primary gene product associated with metastasis and migration.
Entity name
Leukemia
Note
SOX4 transcript is found in high levels in B-ALL and T-ALL, but not in AML, CML, CLL, Sezary syndrome, or T cell prolymphocytic leukemia (Mallampati et al., 2008). Retroviral tagging in mouse models suggests a functional role for SOX4 in hematologic malignancies (Shin et al., 2004; Suzuki et al., 2002; Lund et al., 2002).
Entity name
Lung Cancer
Note
SOX4 is upregulated is a significant percentage of lung cancers (Bangur et al., 2002; Friedman et al., 2004) and antibodies to this protein can be found in the serum of lung cancer patients (Friedman et al., 2004).
Entity name
Hepatocellular Carcinoma
Note
Experimental manipulation of SOX4 in hepatocellular carcinoma cell line models suggests that SOX4 is pro-apoptotic in this tumor type (Ahn et al., 2002). Paradoxically, another group found that knocking down SOX4 expression in a hepatocellular carcinoma cell line decreased tumorigenicity (Liao et al., 2008).
Entity name
Medulloblastoma
Note
SOX4 is significantly overexpressed in medulloblastoma compared to normal cerebellum and ependymoma (de Bont et al., 2008; Yokota et al., 2004).
Prognosis
A trend was found towards increased survival with increased levels of expression of SOX4.
Entity name
Prostate Cancer
Note
SOX4 has been show to be over-expressed in prostate tumor samples by microarray analysis, real-time PCR and immunohistochemistry. Additionally, stable transfection of Sox4 into non-transformed prostate cells form colonies in soft agar, suggesting SOX4 can be a transforming oncogene.

Bibliography

Pubmed IDLast YearTitleAuthors

Other Information

Locus ID:

NCBI: 6659
MIM: 184430
HGNC: 11200
Ensembl: ENSG00000124766

Variants:

dbSNP: 6659
ClinVar: 6659
TCGA: ENSG00000124766
COSMIC: SOX4

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000124766ENST00000244745Q06945

Expression (GTEx)

0
10
20
30
40
50
60
70

Pathways

PathwaySourceExternal ID
MicroRNAs in cancerKEGGhsa05206
MicroRNAs in cancerKEGGko05206
Signal TransductionREACTOMER-HSA-162582
Signaling by WntREACTOMER-HSA-195721
TCF dependent signaling in response to WNTREACTOMER-HSA-201681
Deactivation of the beta-catenin transactivating complexREACTOMER-HSA-3769402

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
194872952009Genomic profiling of microRNAs in bladder cancer: miR-129 is associated with poor outcome and promotes cell death in vitro.146
166187202006Sex-determining region Y box 4 is a transforming oncogene in human prostate cancer cells.125
198876232009Epigenetic repression of microRNA-129-2 leads to overexpression of SOX4 oncogene in endometrial cancer.105
227871202012SOX4 induces epithelial-mesenchymal transition and contributes to breast cancer progression.93
233897312013MicroRNA-138 suppresses ovarian cancer cell invasion and metastasis by targeting SOX4 and HIF-1α.84
191475882009Genome-wide promoter analysis of the SOX4 transcriptional network in prostate cancer cells.83
288109272017STAT3-mediated upregulation of lncRNA HOXD-AS1 as a ceRNA facilitates liver cancer metastasis by regulating SOX4.78
185044332008Identification of SOX4 target genes using phylogenetic footprinting-based prediction from expression microarrays suggests that overexpression of SOX4 potentiates metastasis in hepatocellular carcinoma.73
200807512010Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3.70
275538542016LncSox4 promotes the self-renewal of liver tumour-initiating cells through Stat3-mediated Sox4 expression.60

Citation

David L Satinover ; Chris A Moskaluk

SOX4 (SRY (sex determining region Y)-box 4)

Atlas Genet Cytogenet Oncol Haematol. 2009-01-01

Online version: http://atlasgeneticsoncology.org/gene/42358/js/lib/favicon/apple-touch-icon.png