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PMID: 20229564 Published · ppublish English Journal Article Review

Small-molecule inhibitors of the hedgehog signaling pathway as cancer therapeutics.

ChemMedChem ·Vol. 5 ·No. 4 ·2010-04-06 ·Pages 500-12

Peukert S, Miller-Moslin K

Abstract

Inhibitors of the Hedgehog (Hh) molecular signaling pathway have emerged in recent years as a promising new class of potential therapeutics for cancer treatment. Numerous drug discovery efforts have resulted in the identification of a wide variety of small molecules that target different members of this pathway, including Smoothened (Smo), Sonic hedgehog protein (Shh), and Gli1. Several Smo inhibitors have now entered human clinical trials, and successful proof-of-concept studies have been carried out in patients with defined genetic mutations in the Hh pathway. This review provides a general overview of three main topics in this rapidly expanding area: 1) the various types of biological assays and in vivo models that have been employed for the identification and optimization of Hh pathway inhibitors; 2) Smo inhibitors reported to date, including recent clinical results where available; and 3) efforts toward the identification and characterization of inhibitors of other members of the Hh pathway.

MeSH Terms
Animals Antineoplastic Agents/chemistry,therapeutic use Cell Line Disease Models, Animal Drug Industry Hedgehog Proteins/antagonists & inhibitors,metabolism Humans Neoplasms/drug therapy Receptors, G-Protein-Coupled/antagonists & inhibitors,metabolism Signal Transduction Small Molecule Libraries/chemistry,therapeutic use Smoothened Receptor
Chemicals
Antineoplastic Agents Hedgehog Proteins Receptors, G-Protein-Coupled SMO protein, human Small Molecule Libraries Smoothened Receptor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Peukert Stefan
Department of Global Discovery Chemistry, Novartis Institutes for Biomedical Research, 250 Massachusetts Avenue, Cambridge, MA 02139, USA. [email protected]
Miller-Moslin Karen
Article Info
Journal
ChemMedChem
Abbr.
ChemMedChem
ISSN
1860-7187
Published
2010-04-06
Pages
500-12
Language
English
Region
Germany
NLM ID
101259013
Subset
IM
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