Gallic acid induces HeLa cell death via increasing GSH depletion rather than ROS levels

  • Woo Hyun Park*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Gallic acid (GA; 3,4,5-triphydroxyl-benzoic acid) is widely dispersed in various plants, fruits and foods and it shows various biological properties including anticancer effects. This study investigated the effects of GA on HeLa cervical cancer cells in relation to cell death, reactive oxygen species (ROS) and glutathione (GSH). GA dose-dependently inhibited the growth of HeLa cells and human umbilical vein endothelial cells (HUVEC) at 24 or 72 h. The susceptibility of HeLa cells to GA was higher than that of HUVEC. GA induced apoptosis in HeLa cells, which was accompanied by the loss of mitochondrial membrane potential (MMP; Δm). GA increased ROS levels including O2 .- in HeLa cells at 24 h and it also induced GSH depletion. N-acetyl cysteine (NAC) increased the growth inhibition of GA-treated HeLa cells and enhanced the death of these cells. NAC differently influenced ROS levels in GA-treated HeLa cells and significantly increased GSH depletion in these cells. L-buthionine sulfoximine (BSO) increased MMP (Δm) loss, ROS levels and GSH depletion in GA-treated HeLa cells. In conclusion, GA significantly inhibited the growth of HeLa cells. GA-induced HeLa cell death was tightly related to GSH depletion rather than ROS level changes.

Original languageEnglish
Pages (from-to)1277-1283
Number of pages7
JournalOncology Reports
Volume37
Issue number2
DOIs
StatePublished - 2017.02

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

  • Cell death
  • Gallic acid
  • Glutathione
  • HeLa
  • Reactive oxygen species

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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