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2000
Volume 6, Issue 4
  • ISSN: 1573-3971
  • E-ISSN: 1875-6360

Abstract

The most severe clinical and pathologic manifestations of systemic sclerosis (SSc) are the result of a fibrotic process characterized by the excessive and often progressive deposition of collagen and other connective tissue macromolecules in skin and numerous internal organs. The mechanisms involved in the initiation and progression of the remarkable fibrotic process in SSc remain largely unknown. Extensive recent studies have indicated that a variety of polypeptide growth factors play a crucial role in this process. The most commonly implicated growth factors include transforming growth factor beta (TGF-β), connective tissue growth factor (CTGF), platelet derived growth factor (PDGF), and vascular endothelial growth factor (VEGF). Here, the experimental evidence supporting the participation of various growth factors in the pathogenesis of the fibrotic process in SSc and the molecular mechanisms involved will be reviewed.

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/content/journals/crr/10.2174/157339710793205611
2010-11-01
2025-05-18
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/content/journals/crr/10.2174/157339710793205611
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  • Article Type:
    Research Article
Keyword(s): (LTBP); (RSmads); activin receptor like kinases; anti-PDGF receptor-specific; anti-PDGFRa; anti-αvβ5 antibody; BAL fluid; c-Abl; Caveolin-1 Regulation; chronic myelogenous leukemia; collagens type; colony-stimulating factor receptor 1; Connective Tissue Growth Factor (CTGF); connective tissue growth factor (CTGF); contractile phenotype; Cytoplasmic Abelson Kinase (c-Abl); EndoMT; extracellular matrix; Fibroblast Growth Factors (FGF); fibrosis; fibrotic diseases; fibrotic process; Global gene expression; growth factor; growth factors; GTPase activa-ting protein (IQGAP); healthy control biopsies; high-resolution expression; IGF-1; IGFBP-3; imatinib mesylate; inflammatory response; Insulin-Like Growth Factor (IGF); intracellular signaling cascades; latency-associated peptide (LAP); malignant cell transformation; myofibroblasts; pathologic organ fibrosis; pathological tissue fibrotic responses; phenotypic transdifferentiation; PI3K/Akt Pathways; platelet derived growth factor (PDGF); Platelet-Derived Growth Factor (PDGF); polypeptide growth; profiling technologies; protein kinase c delta; reactive oxygen radicals (ROS); SARA; selective tyrosine kinase inhibitors; serum autoantibodies; SSc Pathogenesis; SSc-associated pulmonary fibrosis; systemic lupus erythematosus; Systemic sclerosis; TGF-β mediated pathways; TGF-β pleotropic effects; TGF-β Signaling; therapeutic target; Transforming Growth Factor Beta (TGF-β); vascular endothelial growth factor (VEGF); Vascular Endothelial Growth Factor (VEGF); vascular morpho-genesis; wound healing; αvβ5 expression; β5 antisense oligonucleotide
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