Signals from within: the DNA-damage-induced NF-kappaB response

Cell Death Differ. 2006 May;13(5):773-84. doi: 10.1038/sj.cdd.4401843.

Abstract

An appropriate response to genotoxic stress is essential for maintenance of genome stability and avoiding the passage to neoplasia. Nuclear factor kappaB (NF-kappaB) is activated as part of the DNA damage response and is thought to orchestrate a cell survival pathway, which, together with the activation of cell cycle checkpoints and DNA repair, allows the cell in cases of limited damage to restore a normal life cycle, unharmed. In this respect, NF-kappaB is one of the main factors accounting for chemotherapy resistance and as such impedes effective cancer treatment, representing an important drug target. Despite this high clinical relevance, signalling cascades leading to DNA damage-induced NF-kappaB activation are poorly understood and the use of highly divergent experimental set-ups in the past led to many controversies in the field. Therefore, in this review, we will try to summarize the current knowledge of distinct DNA damage-induced NF-kappaB signalling pathways.

Publication types

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

MeSH terms

  • Apoptosis
  • Ataxia Telangiectasia Mutated Proteins
  • Casein Kinase II / metabolism
  • Cell Cycle Proteins / metabolism
  • Cell Survival
  • DNA Damage*
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation*
  • Humans
  • I-kappa B Kinase / metabolism
  • Models, Biological
  • NF-kappa B / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositol 3-Kinases / physiology
  • Protein-Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins c-rel / metabolism
  • Signal Transduction*
  • Tumor Suppressor Proteins / metabolism

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • NF-kappa B
  • Proto-Oncogene Proteins c-rel
  • Tumor Suppressor Proteins
  • Phosphatidylinositol 3-Kinases
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • Casein Kinase II
  • Protein-Serine-Threonine Kinases
  • I-kappa B Kinase