Lycopene inhibits Helicobacter pylori-induced ATM/ATR-dependent DNA damage response in gastric epithelial AGS cells

• Published in: Free radical biology & medicine 2012-02, Vol.52 (3), p.607-615
• Main Authors: Jang, Sung Hee, Lim, Joo Weon, Morio, Tomohiro, Kim, Hyeyoung
• Format: Article
• Language: English
• Subjects: antioxidant activity; antioxidants; Apoptosis; Apoptosis Regulatory Proteins - metabolism; Ataxia Telangiectasia Mutated Proteins; Carotenoids - pharmacology; Cell Cycle; Cell Cycle Proteins - metabolism; Cell Line; Cell Proliferation; Cell Survival; cell viability; cultured cells; DNA damage; DNA Fragmentation; DNA repair; DNA-Binding Proteins - metabolism; Epithelial Cells - metabolism; Epithelial Cells - microbiology; Free Radical Scavengers - pharmacology; Gastric Mucosa - pathology; Helicobacter; Helicobacter Infections - metabolism; Helicobacter Infections - microbiology; Helicobacter pylori; histones; Humans; interphase; lycopene; oxidative stress; Oxidative Stress - drug effects; pathogenesis; Phosphorylation; Protein-Serine-Threonine Kinases - metabolism; reactive oxygen species; Reactive Oxygen Species - metabolism; Tumor Suppressor Proteins - metabolism
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2011.11.010

Oxidative stress linked to DNA damage is involved in the pathogenesis of Helicobacter pylori-associated gastric diseases. The DNA damage response (DDR) coordinates cell-cycle transitions, DNA repair, and apoptosis through the activation of ataxia–telangiectasia-mutated (ATM) and ATM and Rad3-related (ATR) and their target proteins. However, neither H. pylori-induced DDR nor the effects of antioxidants on the DNA damage have been established. This study aimed to investigate the detailed process of H. pylori-induced DNA damage and to examine whether lycopene, a natural antioxidant, inhibits DNA damage and cellular response of gastric epithelial AGS cells infected with H. pylori. AGS cells were cultured with H. pylori in Korean isolates and treated with or without lycopene. Cell viability, DNA damage indices, levels of 8-OH-dG, and reactive oxygen species (ROS) as well as cell-cycle distributions were determined. The activation of ATM, ATR, Chk1, and Chk2; histone H2AX focus formation; activation and induction of p53; and levels of Bax and Bcl-2 and poly(ADP-ribose) polymerase-1 (PARP-1) were assessed. The results showed that H. pylori induced apoptosis in AGS cells with increased Bax and decreased Bcl-2 expression as well as PARP-1 cleavage. Culture with H. pylori led to increases in intracellular ROS, 8-OH-dG, double-strand DNA breaks (DSBs), and DNA fragmentation. H. pylori induced activation of the ATM/Chk2 and ATR/Chk1 pathways, phosphorylation of H2AX and p53, and a delay in the progression of the cells entering the S phase. Lycopene inhibited H. pylori-induced increases in ROS, apoptosis, alterations in cell-cycle distribution, DSBs, and ATM- and ATR-mediated DDR in AGS cells. In conclusion, lycopene may be beneficial for treatment of H. pylori-induced gastric diseases associated with oxidative DNA damage.