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Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma

Basal cell carcinoma (BCC) is the most common nonmelanoma skin cancer. If left untreated, BCCs can become locally aggressive or even metastasize. Currently available treatments include local destruction, surgery, and radiation. Systemic options for advanced disease are limited. The Hedgehog (Hh) pat...

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Autores principales: Doan, Hung Q, Silapunt, Sirunya, Migden, Michael R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028081/
https://www.ncbi.nlm.nih.gov/pubmed/27695345
http://dx.doi.org/10.2147/OTT.S108171
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author Doan, Hung Q
Silapunt, Sirunya
Migden, Michael R
author_facet Doan, Hung Q
Silapunt, Sirunya
Migden, Michael R
author_sort Doan, Hung Q
collection PubMed
description Basal cell carcinoma (BCC) is the most common nonmelanoma skin cancer. If left untreated, BCCs can become locally aggressive or even metastasize. Currently available treatments include local destruction, surgery, and radiation. Systemic options for advanced disease are limited. The Hedgehog (Hh) pathway is aberrantly activated in a majority of BCCs and in other cancers. Hh pathway inhibitors are targeted agents that inhibit the aberrant activation of the Hh pathway, with smoothened being a targeted component. Sonidegib is a novel smoothened inhibitor that was recently approved by the US Food and Drug Administration. This review focuses on BCC pathogenesis and the clinical efficacy of sonidegib for the treatment of advanced BCC.
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spelling pubmed-50280812016-09-30 Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma Doan, Hung Q Silapunt, Sirunya Migden, Michael R Onco Targets Ther Review Basal cell carcinoma (BCC) is the most common nonmelanoma skin cancer. If left untreated, BCCs can become locally aggressive or even metastasize. Currently available treatments include local destruction, surgery, and radiation. Systemic options for advanced disease are limited. The Hedgehog (Hh) pathway is aberrantly activated in a majority of BCCs and in other cancers. Hh pathway inhibitors are targeted agents that inhibit the aberrant activation of the Hh pathway, with smoothened being a targeted component. Sonidegib is a novel smoothened inhibitor that was recently approved by the US Food and Drug Administration. This review focuses on BCC pathogenesis and the clinical efficacy of sonidegib for the treatment of advanced BCC. Dove Medical Press 2016-09-14 /pmc/articles/PMC5028081/ /pubmed/27695345 http://dx.doi.org/10.2147/OTT.S108171 Text en © 2016 Doan et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Doan, Hung Q
Silapunt, Sirunya
Migden, Michael R
Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
title Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
title_full Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
title_fullStr Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
title_full_unstemmed Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
title_short Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
title_sort sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028081/
https://www.ncbi.nlm.nih.gov/pubmed/27695345
http://dx.doi.org/10.2147/OTT.S108171
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