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Open AccessJournal ArticleDOI

Fibroblast growth factors, their receptors and signaling.

Ciaran Powers, +2 more
- 01 Sep 2000 - 
- Vol. 7, Iss: 3, pp 165-197
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TLDR
FGF signaling also appears to play a role in tumor growth and angiogenesis, and autocrine FGF signaling may be particularly important in the progression of steroid hormone-dependent cancers to a hormone-independent state.
Abstract
Fibroblast growth factors (FGFs) are small polypeptide growth factors, all of whom share in common certain structural characteristics, and most of whom bind heparin avidly. Many FGFs contain signal peptides for secretion and are secreted into the extracellular environment, where theycan bind to the heparan-like glycosaminoglycans (HLGAGs) of the extracellular matrix (ECM). From this reservoir, FGFs mayact directlyon target cells, or theycan be released through digestion of the ECM or the activityof a carrier protein, a secreted FGF binding protein. FGFs bind specific receptor tyrosine kinases in the context of HLGAGs and this binding induces receptor dimerization and activation, ultimatelyresulting in the activation of various signal transduction cascades. Some FGFs are potent angiogenic factors and most playimportant roles in embry onic development and wound healing. FGF signaling also appears to playa role in tumor growth and angiogenesis, and autocrine FGF signaling maybe particularlyimportant in the progression of steroid hormone-dependent cancers to a hormone-independent state.

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Citations
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Effect of human S100A13 gene silencing on FGF-1 transportation in human endothelial cells.

TL;DR: Lentiviral RNAi vectors induced suppression efficiency of S100A13 gene by 90% in HUVECs, suggesting that S 100A13 is a key cargo protein for FGF-1 release.
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A novel FGF2 antagonist peptide P8 with potent antiproliferation activity.

TL;DR: A novel FGF2-binding short peptide (P8, PLLQATAGGGS-NH2) is identified using phage display technology and alanine scanning and implied that P8 peptide may develop as a multi-target antagonist peptide contributing to tumor treatment.
Dissertation

Role of transglutaminases in signalling that regulates epithelial responses in wound healing

TL;DR: This thesis confirms the presence of GPR56 in keratinocytes and indicates it may be involved in Keratinocyte migration and proliferation.

The Effect of Valdecoxib on the Production of Growth Factors Evoked by Hypoxia and Bacterial Lipopolysaccharide in HMEC-1 Cells* Wpływ waldekoksybu na wydzielanie czynników wzrostu wywołane hipoksją i bakteryjnym lipopolisacharydem w komórkach HMEC-1

TL;DR: In this article, a selective COX-2 inhibitor, Valdecoxib, was applied to normal human microvascular endothelial cells (HMEC-1) in the presence of 100 µg/mL LPS or 200 µm CoCl2.
Patent

FGFR4 inhibitor, preparation method therefor and pharmaceutical use thereof

TL;DR: In this article, an FGFR4 inhibitor having the structure of formula (I) and a preparation method therefor and the use thereof is provided. And the compound has a very strong inhibitory effect on FGFR 4 kinase activity and has a high selectivity, and can be widely used in the preparation of a drug for treating cancers.
References
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Journal ArticleDOI

Cell surface, heparin-like molecules are required for binding of basic fibroblast growth factor to its high affinity receptor.

TL;DR: It is demonstrated that free heparin and heparan sulfate can reconstitute a low affinity receptor that is, in turn, required for the high affinity binding of bFGF.
Journal ArticleDOI

Protein modules and signalling networks

TL;DR: This work highlights conserved protein domains that act as key regulatory participants in many of these different signalling pathways in multicellular organisms.
Journal ArticleDOI

Thalidomide is an inhibitor of angiogenesis.

TL;DR: Electron microscopic examination of the corneal neovascularization of thalidomide-treated rabbits revealed specific ultrastructural changes similar to those seen in the deformed limb bud vasculature of Thalidomid-treated embryos.
Journal ArticleDOI

Receptor specificity of the fibroblast growth factor family.

TL;DR: It is demonstrated that FGF 1 is the only FGF that can activate all FGF receptor splice variants and the relative activity of all the other members of the FGF family is determined.
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