The nitroxide tempol induces oxidative stress, p21(WAF1/CIP1), and cell death in HL60 cells

Free Radic Biol Med. 2000 Oct 1;29(7):633-41. doi: 10.1016/s0891-5849(00)00347-6.

Abstract

The antiproliferative effect of Tempol, a stable nitroxide free radical, was investigated on the p53-negative human leukemia cell line HL60. A concentration- and time-dependent inhibition of cell growth was observed that appears to be due to induction of apoptosis. Involvement of oxidative stress is indicated by a concentration-dependent increase in intracellular peroxides and a parallel decrease in total cellular glutathione; in addition, increased survival rates were observed in cells simultaneously treated with Tempol and the antioxidant N-acetylcysteine. Tempol did not affect the relative levels of Bax and Bcl2, whereas p21(WAF1/CIP1) was enhanced in a concentration- and time-dependent fashion; this effect was partially inhibited by N-acetylcysteine, was maintained for up to 8 h after Tempol removal, and seemed to depend on continuing protein synthesis. The increase in p21(WAF1/CIP1) was accompanied by a parallel accumulation of cells in the G(1) phase of the cycle and by a decrease in the 110 kDa form of pRb. Our results suggest that p53-independent induction of p21(WAF1/CIP1) mediates the antiproliferative effect of Tempol; on the basis of this observation, the nitroxide could be proposed as an useful adjunct to the treatment of p53-deficient tumors, which are often refractory to standard chemotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / pharmacology
  • Antioxidants / pharmacology
  • Apoptosis / drug effects*
  • Cell Cycle / drug effects*
  • Cell Division / drug effects
  • Cell Survival / drug effects
  • Cyclic N-Oxides / toxicity*
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / metabolism*
  • Glutathione / metabolism
  • HL-60 Cells
  • Humans
  • Oxidative Stress / drug effects*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Spin Labels
  • bcl-2-Associated X Protein

Substances

  • Antioxidants
  • BAX protein, human
  • CDKN1A protein, human
  • Cyclic N-Oxides
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Spin Labels
  • bcl-2-Associated X Protein
  • Glutathione
  • tempol
  • Acetylcysteine