Functional gene polymorphisms and expression alteration of selected microRNAs and the risk of various gastric lesions in Helicobacter pylori-related gastric diseases
0301 basic medicine
single nucleotide polymorphisms
03 medical and health sciences
microRNA
Helicobacter pylori
Genetics
interaction
gastric disease
QH426-470
3. Good health
DOI:
10.3389/fgene.2022.1097543
Publication Date:
2023-01-12T07:01:18Z
AUTHORS (12)
ABSTRACT
Background:Helicobacter pylori (Hp) persistent infection is an important pathogenic factor for a series of chronic gastric diseases from gastritis to cancer. Genetic and epigenetic abnormalities microRNAs may play vital role in the pathological evolution mucosa Helicobacter pylori-related (HPGD). This study aimed investigate relationship between miR-146a, miR-196a2, miR-149, miR-499 miR-27a gene single nucleotide polymorphisms (SNPs) their expressions with changes mucosa, further analyze interactions SNPs Hp. Methods: Subjects this included patients diagnosed HPGD healthy controls. MiR-146a rs2910164, miR-196a2 rs11614913, miR-149 rs2292832, rs3746444 rs895819 were genotyped by direct sequencing. Fluorescence quantitative PCR was used detect microRNA expressions. Gene-gene gene-environment evaluated multifactor dimensionality reduction (MDR) method. Results: we found that frequency distribution rs11614913 CT genotype precancerous lesion (GPL) group cancer (GC) significantly higher than normal control (NOR) [adjusted OR = 6.16, 95%CI (1.46-26.03); adjusted 11.83, (1.65-84.72), respectively]. C allele associated increased risk GC 10.14, (2.25-45.77); 3.71, 95%CI(1.46-9.44), The MDR analysis results showed interaction Hp GPL (p 0.004). Meanwhile, expression level NOR, inflammation (CI) early (EPL) groups among Hp-positive subjects. And both EPL group. Also, CI atrophy (GA) groups. Conclusion: affect genetic susceptibility or GC. MiR-196a2 have synergistic effect occurrence development GPL. up-regulation miR-499, caused be mechanism carcinogenesis.
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