TY - JOUR
T1 - Sonic hedgehog in gastric physiology and neoplastic transformation
T2 - Friend or foe?
AU - El-Zaatari, Mohamad
AU - Saqui-Salces, Milena
AU - Waghray, Megna
AU - Todisco, Andrea
AU - Merchant, Juanita L.
PY - 2009/2
Y1 - 2009/2
N2 - Purpose of review: To understand the role of sonic hedgehog (Shh) in normal gastric physiology and neoplastic transformation. Recent findings: Emerging evidence shows that gastric epithelial cells produce Shh ligand, which subsequently targets the mesenchyme. This paracrine signaling event is recapitulated by Shh-producing tumors that signal to the supporting stroma to encourage growth. Primary cilia contain components of the hedgehog signaling apparatus, and thus are typically found on responding stromal cells. Summary: In the stomach, Shh is produced in epithelial cells and received by responding cells in the mesenchyme. In vitro, Shh enhances gastric acid secretion and induces mucin expression. It remains to be determined whether the canonical signaling pathway mediates the observed epithelial effects. Shh expression and signaling is reduced in chronic gastritis, and Shh-/- embryos exhibit hyperplasia and metaplastic changes in the gastric mucosa. After its loss in the corpus, Shh is re-expressed in some gastric carcinomas typically arising in the distal stomach or antrum, suggesting that it promotes tumor growth.
AB - Purpose of review: To understand the role of sonic hedgehog (Shh) in normal gastric physiology and neoplastic transformation. Recent findings: Emerging evidence shows that gastric epithelial cells produce Shh ligand, which subsequently targets the mesenchyme. This paracrine signaling event is recapitulated by Shh-producing tumors that signal to the supporting stroma to encourage growth. Primary cilia contain components of the hedgehog signaling apparatus, and thus are typically found on responding stromal cells. Summary: In the stomach, Shh is produced in epithelial cells and received by responding cells in the mesenchyme. In vitro, Shh enhances gastric acid secretion and induces mucin expression. It remains to be determined whether the canonical signaling pathway mediates the observed epithelial effects. Shh expression and signaling is reduced in chronic gastritis, and Shh-/- embryos exhibit hyperplasia and metaplastic changes in the gastric mucosa. After its loss in the corpus, Shh is re-expressed in some gastric carcinomas typically arising in the distal stomach or antrum, suggesting that it promotes tumor growth.
KW - Hypochlorhydria
KW - Inflammation
KW - Metaplasia
KW - Paracrine
KW - Stomach cancer
UR - http://www.scopus.com/inward/record.url?scp=58849108264&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=58849108264&partnerID=8YFLogxK
U2 - 10.1097/MED.0b013e328320a821
DO - 10.1097/MED.0b013e328320a821
M3 - Review article
C2 - 19104239
AN - SCOPUS:58849108264
SN - 1752-296X
VL - 16
SP - 60
EP - 65
JO - Current Opinion in Endocrinology, Diabetes and Obesity
JF - Current Opinion in Endocrinology, Diabetes and Obesity
IS - 1
ER -