Species: Hu
Applications: Flow
Host: Mouse Monoclonal
Species: Hu
Applications: Flow
Host: Mouse Monoclonal
Species: Hu
Applications: Bioactivity
Species: Hu
Applications: Bioactivity
Species: Hu
Applications: Bioactivity
Description
Fibroblast
growth factor receptor 1 (FGFR1) belongs to a family of type I transmembrane
tyrosine kinases which mediate the biological functions of FGFs that are
involved in a multitude of physiological and pathological cellular processes (1).
The FGFR family is comprised of 4
structurally conserved members (FGFR1-4) all possessing an extracellular
domain (ECD) with three immunoglobulin (Ig)-like domains, an acid-box region
containing a run of acidic residues between the IgI and IgII domains, a
transmembrane domain and cytoplasmic split tyrosine-kinase domain (1, 2). The ECD of
mature, full-length FGFR1 shares 98% amino acid sequence identity with mouse
FGFR1. Alternative splicing generates
multiple forms of FGFR1-3, each with unique signaling characteristics (1-3).
For FGFR1, alternative splicing of the ECD generates FGFR1A, FGFR1B, and FGFR1G
isoforms of the receptor with the A isoform containing three Ig domains, while
the B and G isoforms lack the N‑terminal IgI domain (3). Additional splicing of
the IgIII domain, results in IIIa, IIIb, or IIIc isoforms (3). Only the alpha
isoform has been identified for FGFR3 and FGFR4 and FGFR4 also lacks the IIIb
and IIIc splicing events (4). The FGFR splice variants also exhibit distinct
and varying binding affinities for different FGF ligands (2). FGFRs mediate the
FGF signaling cascade which regulate developmental processes including cellular
proliferation, differentiation, and migration, morphogenesis, and patterning (5).
FGFRs transduce the signals through three dominant pathways including RAS/MAPK,
PI3k/AKT, and PLC gamma (6). FGFR1 the most abundant FGFR and is widely expressed in
many adult human tissues, but the splice variants display distinct
tissue-specific differences with IIIc splice variants expressed in mesenchymal
tissue (4, 7, 8). Mutations in FGFR1 or misregulation of FGFR1 mediated
signaling is found in multiple diseases, with FGFR1A(IIIc) specifically upregulated, from
breast and pancreatic cancer to Pfeiffer syndrome and osteoarthritis (4, 9-11).
A soluble version of the FGFR1A(IIIc) splice variant has shown anti-angiogenic
and anti-proliferative properties in multiple cancer cell line models (11).
Bioinformatics
| Uniprot |
|
| Product By Gene ID |
2260 |
| Alternate Names |
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