Anthocyanin-rich haskap (Lonicera caerulea L.) berry extracts reduce nitrosamine-induced DNA damage in human normal lung epithelial cells in vitro

Food Chem Toxicol. 2020 Jul:141:111404. doi: 10.1016/j.fct.2020.111404. Epub 2020 May 13.

Abstract

Diets rich in polyphenols are known to reduce cancer among high-risk populations. Haskap (Lonicera caerulea L.) berry has abundant phenolic acids and flavonoids, especially anthocyanins. Tobacco-specific nitrosamine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) present in cigarette smoke, is a major lung carcinogenic factor. We analyzed the efficacy of anthocyanin-rich haskap berry extracts in preventing DNA damage induced by 4-[(acetoxymethyl) nitrosamino]-1-(3-pyridyl)-1-butanone (NNKOAc), a precursor of NKK, in human lung epithelial BEAS-2B cells in vitro. A cocktail of monomeric polyphenols from haskap berries was extracted separately in ethanol and water and profiled. Sub-lethal concentrations of NNKOAc were used to induce DNA damage in BEAS-2B cells, and a cell viability assay was performed to confirm that the tested concentrations of haskap extracts were not cytotoxic to BEAS-2B cells. Cells were pre-treated with the haskap extracts prior to NNKOAc exposure. Dose-dependent DNA damage was observed with carcinogenic NNKOAc, but did not occur in the presence of the haskap extracts. Pre-treatment of the cells with the haskap extracts significantly reduced NNKOAc-induced DNA damage, DNA fragmentation, and intracellular reactive oxygen species and upregulated the ATM-dependent DNA damage repair cascade compared to non-treated BEAS-2B cells. The protective effect of haskap extracts could be related to their polyphenol content and high antioxidant capacity.

Keywords: Blue honeysuckle; Cancer; Cyanidin-3-O-Glucoside; DNA damage; Genoprotectant; Nitrosamine; Tobacco.

MeSH terms

  • Antioxidants / pharmacology
  • Carcinogens / toxicity*
  • Cell Line
  • DNA Damage / drug effects*
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Histones / metabolism
  • Humans
  • In Vitro Techniques
  • Lonicera / metabolism*
  • Lung / drug effects*
  • Lung / metabolism
  • Nitrosamines / toxicity*
  • Plant Extracts / pharmacology*

Substances

  • Antioxidants
  • Carcinogens
  • H2AX protein, human
  • Histones
  • Nitrosamines
  • Plant Extracts