MAPK inhibitors augment gallic acid-induced A549 lung cancer cell death through the enhancement of glutathione depletion

  • Woo Hyun Park*
  • , Suhn Hee Kim
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Gallic acid (GA) is involved in various biological processes such as cell growth inhibition and apoptosis through changes in reactive oxygen species (ROS). In the present study, we investigated the effects of MAPK (MEK, JNK or p38) inhibitors on cell death in GA-induced A549 lung cancer cells in relation to ROS and glutathione (GSH). Treatment with 100 μM GA inhibited the growth of A549 cells and induced apoptosis and/or necrosis, which was accompanied by the loss of mitochondrial membrane potential (MMP; ΔΨm). GA increased ROS levels as well as GSH depletion in A549 cells at 24 h. MEK inhibitor seemed to enhance cell growth inhibition by GA. This inhibitor also increased cell death, MMP (ΔΨm) loss and GSH depletion in GA-treated A549 cells. Both JNK and p38 inhibitors intensified growth inhibition, cell death, MMP (ΔΨm) loss and GSH depletion by GA. However, none of the MAPK inhibitors significantly altered ROS levels in GA-treated A549 cells. In conclusion, MAPK inhibitors enhanced growth inhibition and death in GA-treated A549 cells, which were correlated with GSH depletion rather than ROS levels.

Original languageEnglish
Pages (from-to)513-519
Number of pages7
JournalOncology Reports
Volume30
Issue number1
DOIs
StatePublished - 2013.07

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • A549
  • Cell death
  • Gallic acid
  • Glutathione
  • Mitogen-activated protein kinase
  • Reactive oxygen species

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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