Hypoxia modulates the antioxidant effect of hydroxytyrosol in MCF-7 breast cancer cells

PLoS One. 2018 Sep 20;13(9):e0203892. doi: 10.1371/journal.pone.0203892. eCollection 2018.

Abstract

Although cancer is multifactorial, a strong correlation between this pathology and increased oxidative stress has long been stablished. Hypoxia, inherent to solid tumors, increases reactive oxygen species and should be taken into account when analyzing the response of tumor cells to antioxidants. The Mediterranean diet has been related to a lower incidence of cancer, and particularly of breast cancer. Given that hydroxytyrosol (HT) is largely responsible for the antioxidant properties of olive oil, we have performed a comprehensive and comparative study of its effect on the oxidative stress response of the human breast cancer cell line MCF-7 in hypoxia and normoxia. Our results demonstrate that the antioxidant action of HT is particularly effective in a hypoxic environment. Moreover, we have observed that this polyphenol modulates the transcription and translation of members of the PGC-1α/ERRα and PGC-1α/Nrf2 pathways. However, while the transcriptional effects of HT are similar in normoxic and hypoxic conditions, its translational action is less prominent and partially attenuated in hypoxia, and therefore cannot completely explain the antioxidant effect of HT. Consequently, our results underscore that the hypoxic environment of tumor cells should be considered when analyzing the effect of bioactive compounds. Besides, this study also points to the importance of assessing the regulatory role of HT at both mRNA and protein level to get a complete picture of its effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants
  • Breast Neoplasms / genetics
  • Cell Line, Tumor
  • ERRalpha Estrogen-Related Receptor
  • Humans
  • Hypoxia / metabolism
  • Hypoxia / physiopathology*
  • MCF-7 Cells / physiology
  • NF-E2-Related Factor 2 / drug effects
  • Olive Oil / pharmacology
  • Oxidative Stress / drug effects
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / drug effects
  • Phenylethyl Alcohol / analogs & derivatives*
  • Phenylethyl Alcohol / metabolism
  • Phenylethyl Alcohol / pharmacology
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Receptors, Estrogen / drug effects
  • Signal Transduction / drug effects

Substances

  • Antioxidants
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Olive Oil
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA, Messenger
  • Reactive Oxygen Species
  • Receptors, Estrogen
  • 3,4-dihydroxyphenylethanol
  • Phenylethyl Alcohol

Grants and funding

The author(s) received no specific funding for this work.