Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/357313
Type: Artigo
Title: Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
Author: Escuin-Ordinas, Helena
Li, Shuoran
Xie, Michael W.
Sun, Lu
Hugo, Willy
Huang, Rong Rong
Jiao, Jing
de-Faria, Felipe Meira
Realegeno, Susan
Krystofinski, Paige
Azhdam, Ariel
Komenan, Sara Marie D.
Atefi, Mohammad
Comin-Anduix, Begona
Pellegrini, Matteo
Cochran, Alistair J.
Modlin, Robert L.
Herschman, Harvey R.
Lo, Roger S.
McBride, William H.
Segura, Tatiana
Ribas, Antoni
Abstract: BRAF inhibitors are highly effective therapies for the treatment of BRAF(V600)-mutated melanoma, with the main toxicity being a variety of hyperproliferative skin conditions due to paradoxical activation of the mitogen-activated protein kinase (MAPK) pathway in BRAF wild-type cells. Most of these hyperproliferative skin changes improve when a MEK inhibitor is co-administered, as it blocks paradoxical MAPK activation. Here we show how the BRAF inhibitor vemurafenib accelerates skin wound healing by inducing the proliferation and migration of human keratinocytes through extracellular signal-regulated kinase (ERK) phosphorylation and cell cycle progression. Topical treatment with vemurafenib in two wound-healing mice models accelerates cutaneous wound healing through paradoxical MAPK activation; addition of a mitogen-activated protein kinase kinase (MEK) inhibitor reverses the benefit of vemurafenib-accelerated wound healing. The same dosing regimen of topical BRAF inhibitor does not increase the incidence of cutaneous squamous cell carcinomas in mice. Therefore, topical BRAF inhibitors may have clinical applications in accelerating the healing of skin wounds
Subject: Marcadores biológicos
Country: Reino Unido
Editor: Nature
Rights: Fechado
Identifier DOI: 10.1038/ncomms12348
Address: https://www.nature.com/articles/ncomms12348
Date Issue: 2016
Appears in Collections:IB - Artigos e Outros Documentos

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