Noxa: at the tip of the balance between life and death

Oncogene. 2008 Dec;27 Suppl 1(Suppl 1):S84-92. doi: 10.1038/onc.2009.46.

Abstract

Among all Bcl2 homology domain 3 (BH3)-only proteins known to date, APR/PMAIP1/Noxa, albeit showing weak proapoptotic potential on its own, appears to be crucial in fine-tuning cell death decisions by targeting the prosurvival molecule Mcl1 for proteasomal degradation. This event appears critical for cell death induction along the mitochondrial Bcl2-regulated apoptosis pathway in response to factor deprivation or DNA damage, presumably by sensitizing the cell toward the action of additional BH3-only protein family members. This review aims to summarize the function of Noxa in normal physiology, stress-induced cell death and tumorigenesis.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis / physiology*
  • Child
  • DNA Damage*
  • Gene Expression Regulation
  • Humans
  • Invertebrates / metabolism
  • Mice
  • Mice, Knockout
  • Molecular Sequence Data
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins / physiology
  • Neoplasms / etiology
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Neoplasms / therapy
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins c-bcl-2 / chemistry
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tumor Suppressor Protein p53 / physiology
  • Vertebrates / metabolism

Substances

  • Mcl1 protein, mouse
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins
  • PMAIP1 protein, human
  • Pmaip1 protein, mouse
  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Suppressor Protein p53
  • Tetradecanoylphorbol Acetate