Fumarate esters as angiogenesis inhibitors: key to action in psoriasis?
- PMID: 21566578
- DOI: 10.1038/jid.2011.45
Fumarate esters as angiogenesis inhibitors: key to action in psoriasis?
Abstract
Fumarate esters--an oral therapy for psoriasis--are used primarily in Europe, but not at all in the United States. Given that biological therapies are exceedingly expensive and pose an increased risk for infections and malignancy, the need for safer and less expensive therapies for psoriasis is compelling. Nonbiological therapies for psoriasis, including methotrexate and systemic retinoids, carry potentially severe side effects and relatively high cost. Fumarate, a natural product that is generated internally in humans during the Krebs cycle, is an attractive alternative to these therapies. However, the mechanism for fumarate's activity in psoriasis remains unknown.
Comment on
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Dimethylfumarate inhibits angiogenesis in vitro and in vivo: a possible role for its antipsoriatic effect?J Invest Dermatol. 2011 Jun;131(6):1347-55. doi: 10.1038/jid.2010.416. Epub 2011 Feb 3. J Invest Dermatol. 2011. PMID: 21289642
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Suppression of VEGFR2 expression in human endothelial cells by dimethylfumarate treatment: evidence for anti-angiogenic action.J Invest Dermatol. 2011 Jun;131(6):1356-64. doi: 10.1038/jid.2011.46. Epub 2011 Mar 24. J Invest Dermatol. 2011. PMID: 21430706
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