| Literature DB >> 27284322 |
Henrique Sulzbach Sulzbach DE Oliveira1, Vanderlei Biolchi2, Helouise Richardt Richardt Medeiros1, Daiane Bizerra Gandor Bizerra Gandor Jantsch1, Luciana Knabben Knabben DE Oliveira Becker Delving2, Roberto Reckziegel3, Márcia Inês Goettert4, Ilma Simoni Brum5, Adriane Pozzobon2.
Abstract
Helicobacter pylori infects ~50% of the world population, causing chronic gastritis and other forms of cellular damage. The present study assessed the influence of H. pylori on the mRNA expression levels of nuclear factor-κB1 (NFKB1), p38α and tumor necrosis factor-α (TNF-α) in human gastric mucosa in a southern Brazilian population. Human gastric tissue was collected by upper endoscopy and H. pylori diagnosis was performed using a rapid urease test and histological analysis. Total RNA was extracted and purified for subsequent cDNA synthesis and analysis by quantitative polymerase chain reaction (qPCR). The gastric tissue samples were divided into four groups as follows: Normal, inactive chronic gastritis, active chronic gastritis and intestinal metaplasia. The SDHA gene was classified as the most stable when compared with ACTB, GAPDH, B2M and HPRT1 genes, and was therefore selected as the reference gene for qPCR data normalization. TNF-α mRNA expression was significantly higher in samples that were positive for H. pylori and with active chronic gastritis. However, no difference was detected in the mRNA expression levels of NFKB1 and p38α between the groups. The present study concluded that the presence of H. pylori is associated with TNF-α upregulation in human gastric mucosa, but had no effect on NFKB1 and p38α mRNA expression levels.Entities:
Keywords: Helicobacter pylori; gastritis; gene expression; inflammation; quantitative polymerase chain reaction
Year: 2016 PMID: 27284322 PMCID: PMC4887776 DOI: 10.3892/etm.2016.3213
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447