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Find STAT3 Products
Interaction Network for STAT3
STAT3 Details
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Related Pathways
JAK/Stat Signaling TREM1 Signaling IL-6 Signaling View All Pathways
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| Synonyms: 1110034C02Rik, acute-phase response factor, APRF, AW109958, FLJ20882, MGC128731, MGC16063, MGC93551, Stat1, STAT3, Stat3 alpha, Stat3 alpha isoform, Stat3 beta isoform, Stat3 delta |
STAT3 Pathway
The four isoforms of STAT3 (Acute Phase Response Factor (APRF)): STAT3alpha (STAT3α); STAT3beta (STATβ); STAT3gamma (STAT3γ) and STAT3delta (STAT3δ) are members of the signal transducers and activators of transcription (STAT) protein family of transcription factors that bind as homo- and/or heterodimers to recognition sites such as the c-sis-inducible element (SIE) or gamma-activated site element (GAS) in gene promoters. STAT3α is expressed in most cells as a full-length isoform. STATβ is truncated alternatively spliced isoform. STAT3γ is produced by proteolysis of STAT3α.
STAT3 proteins are activated by a wide range of cytokines and growth factors. Cytokines typically activate STAT3 proteins through the JAK family of tyrosine kinases. STAT3 proteins are also activated via cytoplasmic kinases of the Src kinase family and by the tyrosine kinase activity of various (TKR) growth factor receptors. STAT3 proteins are differentially activated by cytokines that utilize the gp130 receptor component. Members of this family include: ciliary neurotrophic factor (CNTF), oncostatin M (OSM), leukemia-inhibitory factor (LIF) and interleukin-6 (IL-6). STAT3 proteins are also activated by growth hormone (GH); thrombopoietin (EPO), GCSF, GM-CSF, bFGF and many of the interleukins.
STAT3 is involved in embryonic stem (ES) cell self-renewal (stemness) of some mammalian cell types and species. In general, STAT3-mediated transcription directs cells into cell survival and cell-cycle progression. STAT3 participates in cellular transformation and tumorigenesis.
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References:
- Barre, B. et. al. (2002) Opposite regulation of myc and p21waf1 transcription by STAT3 proteins. J. Biol. Chem. 278, 2990-2996.
- Burdon, T. et. al. (2002) Signalling, cell cycle and pluripotency in embryonic stem cells. Trends Cell Biol. 12, 432-438.
- Daheron, L. et. al. (2004) LIF/STAT3 signaling fails to maintain self-renewal of human embryonic stem cells. Stem Cells 22, 770-778.
- Lin, Q. et. al. (2005) Constitutive activation of JAK3/STAT3 in colon carcinoma tumors and cell lines: inhibition of JAK3/STAT3 signaling induces apoptosis and cell cycle arrest of colon carcinoma cells. Am, J. Pathol. 167, 969-980.
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Content for this page is provided by Dennis R. Conrad, Ph.D., a Life Science industry consultant with over 25 years of experience in the formulation and optimization of cell culture media. Dr. Conrad's email address is biomediaexpert@earthlink.net
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