BACKGROUND/AIMS: This study was aimed to investigate the polymorphism of interleukin-1beta(IL-1B) and IL-1 receptor antagonist (IL-1RN) gene and the relationship between genotypes and development of gastric adenocarcinoma in Korean, and to investigate the role of Helicobactor pylori (H. pylori) infection. METHODS: The study population comprised of 258 patients with gastric adenocarcinoma. They were classified according to Lauren's classification and the status of H. pylori infection. Genomic DNA was extracted from the gastric tissue. As a control, genomic DNA from peripheral lymphocyte of 100 healthy individuals was used. The amplified products of -511 bp and -31 bp fragments in the IL-1B by PCR were digested by restriction enzyme and separated for RFLP. Variable number tandem repeats were amplified and subjected to RFLP of IL-1RN. RESULTS: There was no significant difference in the genotype of IL-1B-511T and IL-1B-31C between the adenocarcinoma group and the control group. IL-1RN allele 1 homozygote in the intestinal type showed high frequency of 91.7% (p=0.007). In the H. pylori-positive group of the adenocarcinoma, the frequency of IL-1B-31C was significantly higher than that of H. pylori-negative group (p=0.045). CONCLUSIONS: The single nucleotide polymorphism of IL-1B-31C may contribute to the development of the gastric adenocarcinoma in the H. pylori-positive population.
Adenocarcinoma/*genetics/microbiology ; Aged ; English Abstract ; Female ; Helicobacter Infections/complications ; Helicobacter pylori ; Humans ; Interleukin-1/*genetics ; Male ; Middle Aged ; *Polymorphism, Single Nucleotide ; Stomach Neoplasms/*genetics/microbiology

OBJECTIVETo investigate the effect of Helicobacter pylori-encoded CagA on biological behavior of gastric adenocarcinoma AGS cells.

METHODSWith experiment-control system of the wild-type CagA positive strain and isogenic CagA negative mutant strain of Helicobacter pyroli (Hp) were used as control and experimental groups, respectively. The cell contact, migration and invasion were examined by light and electron microscopy and invasion assay.

RESULTSThe AGS cells infected by Hp strain with positive wild-type CagA showed more severely changed tight junction, wider intercellular space, loss of cell contacts, and higher migrating and invasive ability.

CONCLUSIONHp CagA may lead to loss of cell contacting and higher migrating and invading ability of gastic cells, and accelerates the malignant progress of tumor.

Adenocarcinoma ; microbiology ; pathology ; ultrastructure ; Antigens, Bacterial ; genetics ; Bacterial Proteins ; genetics ; Cell Line, Tumor ; Cell Movement ; Extracellular Space ; Helicobacter pylori ; genetics ; pathogenicity ; Humans ; Intercellular Junctions ; ultrastructure ; Mutation ; Stomach Neoplasms ; microbiology ; pathology ; ultrastructure

Several species of Helicobacter colonize the hepatobiliary tract of animals and cause hepatobiliary diseases. The aim of this study is to investigate Helicobacter found in the biliary tract diseases of humans. Thirty-two bile samples (15 from bile duct cancer, 6 from pancreatic head cancer, and 11 from intrahepatic duct stone) were obtained by percutaneous transhepatic biliary drainage. Polymerase chain reaction analysis using Helicobacter specific urease A gene and 16S rRNA primers, bile pH measurement, and Helicobacter culture were performed. Helicobacter DNA was detected in 37.5%, and 31.3% by PCR with ureA gene, and 16S rRNA, respectively. The bile pH was not related to the presence of Helicobacter. The cultures were not successful. In conclusion, Helicobacter can be detected in the bile of patients with bile duct diseases. The possibility of pathogenesis of biliary tract diseases in humans by these organisms will be further investigated.
Adenocarcinoma/microbiology ; Adult ; Aged ; Aged, 80 and over ; Bile/microbiology* ; Bile Duct Diseases/microbiology* ; Bile Duct Neoplasms/microbiology ; Cholelithiasis/microbiology ; DNA Primers ; DNA, Bacterial* ; Helicobacter/isolation & purification* ; Helicobacter/growth & development ; Helicobacter/genetics ; Human ; Hydrogen-Ion Concentration ; Middle Age ; Pancreatic Neoplasms/microbiology ; Polymerase Chain Reaction