Abstract
Infection with Helicobacter pylori has been associated with the development of gastric adenocarcinoma in humans. Several routes have been implicated, the main one being oxidative DNA damage resulting from chronic inflammation, which accompanies infection. However, DNA has been demonstrated in human cells after in vitro incubation with H. pylori sonicates. Using the fragment length analysis using restriction enzymes (FLARE) assay, this study investigates the DNA damaging potential of three clinical isolates of H. pylori on cultured HT29 cells. Significant amounts of oxidative DNA damage were detected in HT29 cells following a 72-hour incubation with each H. pylori isolate. As tumour induction is a known consequence of oxidative DNA damage, chronic infection with the organism may lead to the development of adenocarcinoma of the stomach.
| Original language | English |
|---|---|
| Pages (from-to) | 149-152 |
| Journal | British Journal of Biomedical Science |
| Volume | 64 |
| Issue number | 4 |
| Publication status | Published - 2007 |
Keywords
- DNA damage
- flare assay
- helicobacter pylori
- oxidative stress
- gastric epithelial-cells
- mammalian-cells
- infection
- stress
- mucosa
- repair
- carcinogenesis
- proliferation
- association
- glutathione
- Other laboratory based clinical subjects