| Literature DB >> 20385363 |
James Kim1, Jean Y Tang, Ruoyu Gong, Jynho Kim, John J Lee, Karl V Clemons, Curtis R Chong, Kris S Chang, Mark Fereshteh, Dale Gardner, Tannishtha Reya, Jun O Liu, Ervin H Epstein, David A Stevens, Philip A Beachy.
Abstract
In a screen of drugs previously tested in humans we identified itraconazole, a systemic antifungal, as a potent antagonist of the Hedgehog (Hh) signaling pathway that acts by a mechanism distinct from its inhibitory effect on fungal sterol biosynthesis. Systemically administered itraconazole, like other Hh pathway antagonists, can suppress Hh pathway activity and the growth of medulloblastoma in a mouse allograft model and does so at serum levels comparable to those in patients undergoing antifungal therapy. Mechanistically, itraconazole appears to act on the essential Hh pathway component Smoothened (SMO) by a mechanism distinct from that of cyclopamine and other known SMO antagonists, and prevents the ciliary accumulation of SMO normally caused by Hh stimulation. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20385363 PMCID: PMC4039177 DOI: 10.1016/j.ccr.2010.02.027
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743