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PMID: 17762891 Published · ppublish English Journal Article

Patching the gaps in Hedgehog signalling.

Nature cell biology ·Vol. 9 ·No. 9 ·2007-09-00 ·Pages 1005-9

Rohatgi R, Scott MP

Abstract

The Hedgehog (Hh) pathway plays central roles in animal development and stem-cell function. Defects in Hh signalling lead to birth defects and cancer in humans. The first and often genetically damaged step in this pathway is the interaction between two membrane proteins - Patched (Ptc), encoded by a tumour suppressor gene, and Smoothened (Smo), encoded by a proto-oncogene. Recent work linking Hh signalling to sterol metabolites and protein-trafficking events at the primary cilium promises to shed light on the biochemical basis of how Patched inhibits Smoothened, and to provide new avenues for cancer treatment.

MeSH Terms
Animals Hedgehog Proteins/metabolism Humans Neoplasms/metabolism,therapy Patched Receptors Proto-Oncogene Mas Receptors, Cell Surface/metabolism Receptors, G-Protein-Coupled/metabolism Signal Transduction/physiology Smoothened Receptor
Chemicals
Hedgehog Proteins MAS1 protein, human Patched Receptors Proto-Oncogene Mas Receptors, Cell Surface Receptors, G-Protein-Coupled SMO protein, human Smoothened Receptor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rohatgi Rajat
Department of Developmental Biology, Howard Hughes Medical Institute, Clark Center West W252, 318 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5439, USA.
Scott Matthew P
Article Info
Journal
Nature cell biology
Abbr.
Nat Cell Biol
ISSN
1465-7392
Published
2007-09-00
Pages
1005-9
Language
English
Region
England
NLM ID
100890575
Subset
IM
Grants
Howard Hughes Medical Institute · United States
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