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The VHL tumor suppressor: master regulator of HIF.

Abstract
Hypoxia-Inducible Factors (HIFs) are heterodimeric oxygen-sensitive basic helix-loop-helix transcription factors that play central roles in cellular adaptation to low oxygen environments. The von-Hippel Lindau tumor suppressor (pVHL) is the substrate recognition component of an E3 ubiquitin ligase and functions as a master regulator of HIF activity by targeting the hydroxylated HIF-alpha subunit for ubiquitylation and rapid proteasomal degradation under normoxic conditions. Mutations in pVHL can be found in familial and sporadic hemangioblastomas, clear cell carcinomas of the kidney, pheochromocytomas and inherited forms of erythrocytosis, illustrating the importance of disrupted molecular oxygen sensing in the pathogenesis of these diseases. Tissue-specific gene targeting of pVHL in mice has demonstrated that efficient execution of HIF proteolysis is critically important for normal tissue physiology, and has provided novel insights into the functional consequences of HIF activation on the cellular and tissue level. Here we focus on the contribution of individual HIF transcription factors to the development of VHL phenotypes and discuss how the pVHL/HIF axis could be exploited pharmacologically.
AuthorsVolker H Haase
JournalCurrent pharmaceutical design (Curr Pharm Des) Vol. 15 Issue 33 Pg. 3895-903 ( 2009) ISSN: 1873-4286 [Electronic] United Arab Emirates
PMID19671042 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Von Hippel-Lindau Tumor Suppressor Protein
Topics
  • Animals
  • Drug Delivery Systems
  • Gene Targeting
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit (metabolism)
  • Mice
  • Mutation
  • Phenotype
  • Ubiquitination (physiology)
  • Von Hippel-Lindau Tumor Suppressor Protein (genetics, metabolism)

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