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SOSTDC1  -  sclerostin domain containing 1

Homo sapiens

Synonyms: CDA019, DKFZp564D206, ECTODIN, Ectodermal BMP inhibitor, Ectodin, ...
 
 
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Disease relevance of SOSTDC1

 

High impact information on SOSTDC1

  • The CAN family can be divided further into four subgroups based on a conserved arrangement of additional cysteine residues-gremlin and PRDC, cerberus and coco, and DAN, together with USAG-1 and sclerostin [2].
  • We analyzed the regulation and function of ectodin in tooth germs [3].
  • Recombinant ectodin protein produced in cultured cells was efficiently secreted as a antagonist [3].
  • Ectodin is intensely expressed in developing ectodermal organs, including teeth, vibrissae, and hair follicles [3].
  • Renal BMP signaling, assessed by phosphorylation of Smad proteins, is significantly enhanced in USAG-1(-/-) mice during renal injury, indicating that the preservation of renal function is attributed to enhancement of endogenous BMP-7 signaling [4].
 

Chemical compound and disease context of SOSTDC1

 

Biological context of SOSTDC1

  • In the early stage of mouse embryogenesis, USAG-1 is expressed in the first and second branchial arches and in metanephros, while in later stages the expression is confined to renal tubules and ameloblasts of teeth [5].
 

Anatomical context of SOSTDC1

  • Uterine sensitization-associated gene-1 (USAG-1) was previously reported as a gene of unknown function, preferentially expressed in sensitized endometrium of the rat uterus [5].
 

Associations of SOSTDC1 with chemical compounds

 

Analytical, diagnostic and therapeutic context of SOSTDC1

References

  1. Changes in blood supply in small hepatocellular carcinoma: correlation of angiographic images and immunohistochemical findings. Toyoda, H., Fukuda, Y., Hayakawa, T., Kumada, T., Nakano, S. J. Hepatol. (1997) [Pubmed]
  2. Comparative genomic analysis of the eight-membered ring cystine knot-containing bone morphogenetic protein antagonists. Avsian-Kretchmer, O., Hsueh, A.J. Mol. Endocrinol. (2004) [Pubmed]
  3. Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot. Laurikkala, J., Kassai, Y., Pakkasjärvi, L., Thesleff, I., Itoh, N. Dev. Biol. (2003) [Pubmed]
  4. Modulator of bone morphogenetic protein activity in the progression of kidney diseases. Yanagita, M. Kidney Int. (2006) [Pubmed]
  5. USAG-1: a bone morphogenetic protein antagonist abundantly expressed in the kidney. Yanagita, M., Oka, M., Watabe, T., Iguchi, H., Niida, A., Takahashi, S., Akiyama, T., Miyazono, K., Yanagisawa, M., Sakurai, T. Biochem. Biophys. Res. Commun. (2004) [Pubmed]
  6. Significance of tumor vascularity as a predictor of long-term prognosis in patients with small hepatocellular carcinoma treated by percutaneous ethanol injection therapy. Toyoda, H., Kumuda, T., Nakano, S., Takeda, I., Sugiyama, K., Kiriyama, S., Sone, Y. J. Hepatol. (1997) [Pubmed]
  7. Clinical utility of Lens culinaris agglutinin-reactive alpha-fetoprotein in small hepatocellular carcinoma: special reference to imaging diagnosis. Kumada, T., Nakano, S., Takeda, I., Kiriyama, S., Sone, Y., Hayashi, K., Katoh, H., Endoh, T., Sassa, T., Satomura, S. J. Hepatol. (1999) [Pubmed]
 
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