Abstract
Transforming growth factor beta (TGF-β) plays a crucial role in the pathogenesis of skin fibrotic diseases by inducing extracellular matrix gene expression and sustaining fibroblast growth and differentiation. Systemic inhibition of TGF-β by different agents has been shown to effectively inhibit fibrosis in different animal models. However, systemic inhibition of TGF-β raises important safety issues because of the pleiotropic physiological effects of this factor.
Targeting of downstream factors specifically involved in TGF-β profibrotic signaling or local targeting of TGF-β represents potential alternatives to systemic inhibitors. Topical application of a short peptide derived from TGF-β1 type III receptor is effective in preventing or ameliorating established fibrosis in a model of bleomycin-induced scleroderma, suggesting that topical application of small anti-TGF-β peptides is a feasible strategy to treat pathological skin scarring and skin fibrotic diseases.
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Dotor, J., Pablos, J.L. (2008). Topical Application of TGF-β1 Peptide Inhibitors for the Therapy of Skin Fibrosis. In: Transforming Growth Factor-β in Cancer Therapy, Volume I. Cancer Drug Discovery and Development. Humana Press. https://doi.org/10.1007/978-1-59745-292-2_44
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DOI: https://doi.org/10.1007/978-1-59745-292-2_44
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