Astrocyte elevated gene-1 (AEG-1): A multifunctional regulator of normal and abnormal physiology

Pharmacol Ther. 2011 Apr;130(1):1-8. doi: 10.1016/j.pharmthera.2011.01.008. Epub 2011 Jan 20.

Abstract

Since its initial identification and cloning in 2002, Astrocyte Elevated Gene-1 (AEG-1), also known as metadherin (MTDH), 3D3 and LYsine-RIch CEACAM1 co-isolated (LYRIC), has emerged as an important oncogene that is overexpressed in all cancers analyzed so far. Examination of a large cohort of patient samples representing diverse cancer indications has revealed progressive increase in AEG-1 expression with stages and grades of the disease and an inverse relationship between AEG-1 expression level and patient prognosis. AEG-1 functions as a bona fide oncogene by promoting transformation. In addition, it plays a significant role in invasion, metastasis, angiogenesis and chemoresistance, all important hallmarks of an aggressive cancer. AEG-1 is also implicated in diverse physiological and pathological processes, such as development, inflammation, neurodegeneration, migraine and Huntington's disease. AEG-1 is a highly basic protein with a transmembrane domain and multiple nuclear localization signals and it is present in the cell membrane, cytoplasm, nucleus, nucleolus and endoplasmic reticulum. In each location, AEG-1 interacts with specific proteins thereby modulating diverse intracellular processes the combination of which contributes to its pleiotrophic properties. The present review provides a snapshot of the current literature along with future perspectives on this unique molecule.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers, Tumor
  • Cell Adhesion Molecules / genetics*
  • Cell Adhesion Molecules / physiology*
  • Gene Expression
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Membrane Proteins
  • Molecular Targeted Therapy
  • Neoplasms / diagnosis
  • Neoplasms / drug therapy
  • Neoplasms / genetics*
  • Neoplasms / metabolism
  • Oncogenes*
  • RNA-Binding Proteins
  • Signal Transduction / physiology

Substances

  • Biomarkers, Tumor
  • Cell Adhesion Molecules
  • Intracellular Signaling Peptides and Proteins
  • MTDH protein, human
  • Membrane Proteins
  • RNA-Binding Proteins