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dc.contributor.authorOrenay-Boyacioglu S,Kasap E,Yuceyar H,Korkmaz M
dc.date.accessioned2023-03-02T11:25:25Z
dc.date.available2023-03-02T11:25:25Z
dc.date.issued2020
dc.identifier.urihttp://hdl.handle.net/20.500.12481/16235
dc.description.abstractInterleukin 12 (IL-12) has a key function in promoting Th1 immune response in the gastrointestinal mucosa. Although cytokine gene polymorphisms are associated with increased risk of gastric cancer (GC), studies on different geographic regions and ethnic groups are not able to draw a consistent result. The current case-control study aims to find out an association between a functional IL-12B rs3212227 polymorphism and the susceptibility and clinical features of the study groups, which are GC, Helicobacter pylori-infected and H. pylori-uninfected intestinal metaplasia (IM). In this study, IL-12B rs3212227 polymorphism was genotyped in 35 GC cases, 25 H. pylori-infected IM patients, 25 H. pylori-uninfected IM patients, and 25 control subjects. PCR-RFLP analysis was performed to find out and compare the polymorphism profiles of case biopsies. There was statistical significance in genotype distributions and allelic frequencies in GC patients with proximal arrest in stomach (p=0.042). The rs3212227 genotypes and allelic frequencies were not correlated with any of the study groups (p>0.05). Other clinical features examined in the GC patients were also not correlated with the rs3212227 genotypes and allelic frequencies (p>0.05). Current findings suggest that IL-12B rs3212227 polymorphism may play a role in GC development. © Serbian Genetics Society.
dc.titleAssociation of interleukin 12B RS3212227 polymorphism with gastric cancer, intestinal metaplasia, and helicobacter pylori infection
dc.identifier.DOI-ID10.2298/GENSR2001115O
dc.identifier.volume52
dc.identifier.issue1
dc.identifier.startpage115
dc.identifier.endpage126
dc.identifier.issn/e-issn0534-0012


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