Kinases as upstream regulators of the HIF system: their emerging potential as anti-cancer drug targets

Curr Pharm Des. 2009;15(33):3867-77. doi: 10.2174/138161209789649358.

Abstract

The hypoxia-inducible factor-1 (HIF-1) is a key regulator in the mammalian response to oxygen deficiency under both physiological and pathological conditions such as cancer. A number of studies indicated an association between tumor hypoxia, increased hypoxia-inducible factor (HIF-1alpha) levels and a poor prognosis. The HIF-1alpha regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation. However, HIFalpha-subunits also respond to various growth factors, hormones, or cytokines under non-hypoxic conditions implicating the involvement of different kinase pathways in their regulation thereby increasing the interest in HIF-1alpha as a new drug target. Herein, we review current knowledge about phosphorylation-dependent HIF-1alpha regulation, HIF-1alpha protein-protein interactions and subcellular localization with emphasis on new therapeutic strategies targeting the HIF pathway.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Cell Hypoxia
  • Drug Delivery Systems
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Neoplasms / drug therapy*
  • Neoplasms / physiopathology
  • Phosphorylation / drug effects
  • Phosphotransferases / antagonists & inhibitors
  • Prognosis
  • Protein Processing, Post-Translational / physiology

Substances

  • Antineoplastic Agents
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Phosphotransferases