CTHRC1 Antibody – Rabbit Polyclonal

This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]

CTHRC1: May act as a negative regulator of collagen matrix deposition. Defects in CTHRC1 may be a cause of Barrett esophagus (BE). A condition characterized by a metaplastic change in which normal esophageal squamous epithelium is replaced by a columnar and intestinal-type epithelium. Patients with Barrett esophagus have an increased risk of esophageal adenocarcinoma. The main cause of Barrett esophagus is gastroesophageal reflux. The retrograde movement of acid and bile salts from the stomach into the esophagus causes prolonged injury to the esophageal epithelium and induces chronic esophagitis, which in turn is believed to trigger the pathologic changes. Genetic variants in CTHRC1 have been found in individuals with Barrett esophagus and are thought to contribute to disease susceptibility. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 8q22.3

Cellular Component: collagen; cytoplasm; extracellular space; proteinaceous extracellular matrix

Molecular Function: frizzled binding; Wnt-protein binding

Biological Process: cell migration; inner ear receptor stereocilium organization and biogenesis; positive regulation of osteoblast differentiation; positive regulation of osteoblast proliferation; positive regulation of protein binding; Wnt receptor signaling pathway, planar cell polarity pathway

Disease: Barrett Esophagus