Fibroblast growth factors (FGFs) are small polypeptide growth factors, all
of whom share in common certain structural characteristics, and most of who
m bind heparin avidly. Many FGFs contain signal peptides for secretion and
are secreted into the extracellular environment, where they can bind to the
heparan-like glycosaminoglycans (HLGAGs) of the extracellular matrix (ECM)
. From this reservoir, FGFs may act directly on target cells, or they can b
e released through digestion of the ECM or the activity of a carrier protei
n, a secreted FGF binding protein. FGFs bind specific receptor tyrosine kin
ases in the context of HLGAGs and this binding induces receptor dimerizatio
n and activation, ultimately resulting in the activation of various signal
transduction cascades. Some FGFs are potent angiogenic factors and most pla
y important roles in embryonic development and wound healing. FGF signaling
also appears to play a role in tumor growth and angiogenesis, and autocrin
e FGF signaling may be particularly important in the progression of steroid
hormone-dependent cancers to a hormone-independent state.