Vitamin C downregulates interleukin-18 production by increasing reactive oxygen intermediate and mitogen-activated protein kinase signalling in B16F10 murine melanoma cells

Melanoma Res. 2003 Dec;13(6):549-54. doi: 10.1097/00008390-200312000-00002.

Abstract

We recently reported that interleukin-18 (IL-18) is highly expressed in malignant skin tumours such as melanomas, and may play a key role in the malignancy of such tumours. This study was designed to investigate the mechanisms of IL-18 regulation by vitamin C in B16F10 murine melanoma cells. Cells were treated with vitamin C, and the expression of IL-18 was measured by reverse transcription-polymerase chain reaction and intracellular flow cytometry analysis. Decreased IL-18 production and a significant reduction in IL-18 mRNA transcript were detected in cells treated with vitamin C. The effect of vitamin C treatment was blocked by the antioxidant N-acetyl-L-cysteine, suggesting that vitamin C affects IL-18 expression by up-regulating intracellular reactive oxygen intermediate (ROI) levels. To investigate whether the mitogen-activated protein kinase (MAPK) signalling pathway is involved in the downregulation of IL-18 production, cells were pretreated with SB203580, an inhibitor of p38 MAPK, prior to the addition of vitamin C. This pretreatment blocked the decrease in IL-18 production. However, vitamin C treatment enhanced the expression of phosphorylated p38 MAPK. Taken together, we conclude that vitamin C increases intracellular ROI levels, and regulates IL-18 production through the MAPK signalling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / pharmacology
  • Animals
  • Antioxidants / pharmacology
  • Ascorbic Acid / metabolism*
  • Ascorbic Acid / pharmacology
  • Blotting, Western
  • Cell Line, Tumor
  • Densitometry
  • Down-Regulation*
  • Enzyme Inhibitors / pharmacology
  • Flow Cytometry
  • Imidazoles / pharmacology
  • Immunoprecipitation
  • Interleukin-18 / biosynthesis*
  • Interleukin-18 / metabolism
  • MAP Kinase Signaling System*
  • Melanoma / metabolism
  • Mice
  • Pyridines / pharmacology
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Skin Neoplasms / metabolism
  • Time Factors
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Antioxidants
  • Enzyme Inhibitors
  • Imidazoles
  • Interleukin-18
  • Pyridines
  • RNA, Messenger
  • Reactive Oxygen Species
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580
  • Ascorbic Acid
  • Acetylcysteine