pVHL's kryptonite: E2-EPF UCP

Cancer Cell. 2006 Aug;10(2):95-7. doi: 10.1016/j.ccr.2006.07.016.

Abstract

E2-EPF ubiquitin carrier protein (UCP) is a member of an E2 family of enzymes that catalyzes the ligation of ubiquitin to proteins targeted for destruction by the proteasome. UCP is overexpressed in common human cancers, suggesting its involvement in oncogenesis, but a physiologic target of UCP has not been identified. In a recent report published in Nature Medicine, Jung et al. identified von Hippel-Lindau (VHL) tumor suppressor protein, which targets the alpha subunit of hypoxia-inducible factor (HIF) for ubiquitin-mediated destruction, as a bona fide substrate of UCP and demonstrated a potential pVHL-HIF pathway-dependent role for UCP in cancer development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Proteasome Endopeptidase Complex / metabolism*
  • Protein Binding
  • Signal Transduction / physiology
  • Ubiquitin-Conjugating Enzymes / physiology*
  • Von Hippel-Lindau Tumor Suppressor Protein / metabolism*

Substances

  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • ubiquitin carrier proteins
  • Ubiquitin-Conjugating Enzymes
  • Von Hippel-Lindau Tumor Suppressor Protein
  • Proteasome Endopeptidase Complex