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Gas1 is a pleiotropic regulator of cellular functions: from embryonic development to molecular actions in cancer gene therapy.

Abstract
Cellular homeostasis is governed by a precise regulation of the molecular mechanisms of action of several proteins in a given time. There is a group of proteins that have a particular role depending on the cellular context in which they are present and are known as pleiotropic proteins. The Gas1 (Growth Arrest Specific 1) gene was isolated from a subtraction library from serum arrested versus growing NIH3T3 mouse fibroblast. Gas1 is a member of the alpha receptors (GFRα) for the family of GDNF ligands (GFL), we have previously shown that Gas1 acts as a negative modulator of the GDNF-induced intracellular signaling and induces cell arrest and apoptosis. This modulating activity is the cause of the capacity of Gas1 to act as a tumor suppressor. On the other hand, several studies have shown the interaction between Gas1 and Hh (Hedgehog) proteins to potentiate the positive regulation of this pathway, which is involved in the development of the nervous system, and in both the origin and progression of different tumors. This review summarizes our current understanding of the structure of Gas1 and the molecular mechanism of action in different cellular functions, both during embryonic development, in the adult and its effects inhibiting cell growth and inducing apoptosis of cancer cells.
AuthorsJosé Segovia, Natanael Zarco
JournalMini reviews in medicinal chemistry (Mini Rev Med Chem) Vol. 14 Issue 14 Pg. 1139-47 ( 2014) ISSN: 1875-5607 [Electronic] Netherlands
PMID25429664 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Cell Cycle Proteins
  • GAS1 protein, human
  • GPI-Linked Proteins
Topics
  • Animals
  • Cell Cycle (genetics)
  • Cell Cycle Proteins (genetics)
  • Cell Line, Tumor
  • Embryonic Development (genetics)
  • GPI-Linked Proteins (genetics)
  • Genetic Pleiotropy (genetics)
  • Genetic Therapy (trends)
  • Humans
  • Neoplasms (genetics, therapy)

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