Quercetin induces necrosis and apoptosis in SCC-9 oral cancer cells

Nutr Cancer. 2005;53(2):220-31. doi: 10.1207/s15327914nc5302_11.

Abstract

Evidence has accumulated that dietary polyphenols, in particular, flavonoids, have protective effects against oral cancer. In this study, we have examined the effects of quercetin, a major dietary flavonoid, on cell growth and necrosis/apoptosis and cell cycle regulation in human oral squamous carcinoma SCC-9 cells. Quercetin induced dose- and time-dependent, irreversible inhibition of cell growth and cellular DNA synthesis. Light microscopy and lactate dehydrogenase measurements showed modifications in the morphology and membrane integrity of these cells after quercetin treatment. Propidium iodide/annexin V staining showed that quercetin induced necrosis at 24 h and 48 h, whereas at 72 h cells underwent apoptosis, correlating with caspase-3 activation. Flow cytometry studies of the cell cycle distribution showed that quercetin induced mainly S-phase arrest. Thymidylate synthase (TS), a key S-phase enzyme, was inhibited in a time- and dose-dependent fashion by quercetin at the protein level. A lack of effect on TS mRNA suggested that TS down-regulation occurred at the translational level. In conclusion, our data support a view that quercetin initially induces a stress response, resulting in necrosis of these oral epithelial cells. Prolonged exposure of the surviving cells to quercetin causes apoptosis, presumably mediated by inhibition of TS protein.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Apoptosis / drug effects*
  • Carcinoma, Squamous Cell / enzymology
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / pathology*
  • Caspase 3
  • Caspases / metabolism
  • Cell Cycle / drug effects*
  • Cell Line, Tumor
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Flow Cytometry
  • Humans
  • Mouth Neoplasms / enzymology
  • Mouth Neoplasms / metabolism
  • Mouth Neoplasms / pathology*
  • Quercetin / pharmacology*
  • Thymidylate Synthase / antagonists & inhibitors*
  • Thymidylate Synthase / drug effects
  • Time Factors
  • Tumor Necrosis Factors / metabolism

Substances

  • Tumor Necrosis Factors
  • DNA
  • Quercetin
  • Thymidylate Synthase
  • CASP3 protein, human
  • Caspase 3
  • Caspases