Sox2: A Regulatory Factor in Tumorigenesis and Metastasis.
HMG domain
Wnt/β-catonin
endodermal-mesenchymal transition
metastasis
overexpression
transcription factor
tumor propagation.
Journal
Current protein & peptide science
ISSN: 1875-5550
Titre abrégé: Curr Protein Pept Sci
Pays: United Arab Emirates
ID NLM: 100960529
Informations de publication
Date de publication:
2019
2019
Historique:
received:
27
09
2018
revised:
17
02
2019
accepted:
12
03
2019
pubmed:
26
3
2019
medline:
7
8
2019
entrez:
26
3
2019
Statut:
ppublish
Résumé
The transcription factor Sox2 plays an important role in various phases of embryonic development, including cell fate and differentiation. These key regulatory functions are facilitated by binding to specific DNA sequences in combination with partner proteins to exert their effects. Recently, overexpression and gene amplification of Sox2 has been associated with tumor aggression and metastasis in various cancer types, including breast, prostate, lung, ovarian and colon cancer. All the different roles for Sox2 involve complicated regulatory networks consisting of protein-protein and protein-nucleic acid interactions. Their involvement in the EMT modulation is possibly enabled by Wnt/ β-catenin and other signaling pathways. There are number of in vivo models which show Sox2 association with increased cancer aggressiveness, resistance to chemo-radiation therapy and decreased survival rate suggesting Sox2 as a therapeutic target. This review will focus on the different roles for Sox2 in metastasis and tumorigenesis. We will also review the mechanism of action underlying the cooperative Sox2- DNA/partner factors binding where Sox2 can be potentially explored for a therapeutic opportunity to treat cancers.
Identifiants
pubmed: 30907312
pii: CPPS-EPUB-97517
doi: 10.2174/1389203720666190325102255
doi:
Substances chimiques
SOXB1 Transcription Factors
0
Wnt Proteins
0
beta Catenin
0
Types de publication
Journal Article
Review
Langues
eng
Pagination
495-504Informations de copyright
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