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Updated: Jan 19, 2026

Gastric Mucosa Quantitative Polymerase Chain Reaction Analysis for Detecting Helicobacter pylori and Antibiotic Resistance
Published on: March 7, 2025
Helicobacter pylori-miRNA interaction in gastric cancer tissues: First prospective study from Turkey
Suleyman Demiryas1, Bekir Kocazeybek2, Mehmet Demirci3
1Department of General Surgery, Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Abstract:
Helicobacter pylori (H. pylori) is involved in the etiology of gastric cancer (GC). miRNAs are short RNAs that regulate gene expression by marking mRNAs for degradation. miRNAs are involved in tumorigenesis, metastasis, and cell proliferation. We aimed to investigate the miRNA expression profiles of tissues from H. pylori (+) and (-) GC patients. Forty GC patients, 20 H. pylori (+) and 20 H. pylori (-), and a healthy control group were included. The miRNA expression levels were investigated by microarrays and quantitative RT-PCR. We detected 9 upregulated and 4 downregulated miRNAs by microarray. We selected 5 upregulated and 5 downregulated miRNAs for the quantitative RT-PCR assay. The relative fold changes of miRNAs in the cancerous tissue and non-tumor mucosa specimens of H. pylori (+) GC patients for hsa-miR-194 were 4.24- and 3.83-fold higher, respectively, whereas the hsa-miR-145 expression levels were downregulated 0.33-fold and 0.43-fold, respectively, in the same group. The presence of H. pylori significantly upregulated hsa-miR-194 and downregulated hsa-miR-145 expression levels in H. pylori (+) GC cases, compared to H. pylori (-) GC cases. Regional differences in the virulence of H. pylori strains may also be involved in the up- or downregulation of miRNA expression levels.
Insights
Helicobacter pylori infection alters microRNA (miRNA) expression in gastric cancer (GC) patients. H. pylori significantly upregulates hsa-miR-194 and downregulates hsa-miR-145 in GC tissues.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Helicobacter pylori (H. pylori) infection is a known risk factor in the development of gastric cancer (GC).
- MicroRNAs (miRNAs) are crucial regulators of gene expression, implicated in various stages of tumorigenesis, including cancer progression and metastasis.
- Understanding miRNA expression patterns in GC associated with H. pylori infection is vital for elucidating disease mechanisms.
Purpose of the Study:
- To investigate and compare miRNA expression profiles in gastric cancer tissues from patients with and without H. pylori infection.
- To identify specific miRNAs whose expression is significantly altered by H. pylori in the context of GC.
Main Methods:
- Microarray analysis was employed to screen miRNA expression profiles in 40 GC patients (20 H. pylori (+) and 20 H. pylori (-)) and a healthy control group.
- Quantitative RT-PCR was utilized to validate the expression levels of selected differentially expressed miRNAs.
Main Results:
- Microarray analysis identified 9 upregulated and 4 downregulated miRNAs.
- Quantitative RT-PCR confirmed significant upregulation of hsa-miR-194 (4.24-fold in tumor, 3.83-fold in non-tumor mucosa) and downregulation of hsa-miR-145 (0.33-fold in tumor, 0.43-fold in non-tumor mucosa) in H. pylori (+) GC patients compared to H. pylori (-) GC patients.
- H. pylori infection status was found to significantly influence the expression levels of hsa-miR-194 and hsa-miR-145.
Conclusions:
- H. pylori infection significantly modulates specific miRNA expression, including hsa-miR-194 and hsa-miR-145, in gastric cancer patients.
- These altered miRNA profiles may play a role in the pathogenesis of H. pylori-associated GC.
- Variations in H. pylori strain virulence could potentially contribute to observed differences in miRNA expression levels.
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