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pmid:32099601
Predication of hub target genes of differentially expressed microRNAs contributing to Helicobacter pylori infection in gastric non-cancerous tissue.
Mohsen Norouzinia · Mona Zamanian Azodi · Diba Najafgholizadeh Seyfi · Ali Kardan · Ali Naseh · Zahra Akbari
Gastroenterology and hepatology from bed to bench · 2019
Paper
partial
Experiment
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Data
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Analysis
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Execution
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Complete file
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Expression modification of non-coding (NC) RNAs in H.pylori infections requires further investigations to provide better understanding of their roles in the body.\nMETHODS: GSE54397, the microRNA microarray dataset, was analyzed by GEO2R, the online GEO database for detection of differentially expressed microRNAs and lastly the potential target genes as well as their associated pathways.\nRESULTS: A total of 244 miRNAs were detected as differentially expressed (p<0.05 and FC>2) in non-cancerous tissue of gastric with H.pylori infection in comparison with tissues without H.pylori infection. The findings indicated that hub microRNAs and target genes of up-regulated network are KIF9, DCTN3, and CA5BP1 along with hsa-miR-519d, hsa-miR-573, hsa-miR-646, hsa-miR-92a-1, hsa-miR-186, and hsa-miR-892a, respectively. For the down-regulated network, genes of RABGAP1, HSPB11 and microRNAs of hsa-miR-620, hsa-miR-19b-2, hsa-miR-555, and hsa-let-7f-2 were hubs. Most of the up-regulated microRNAs are involved in gastric cancer development while there is no evidence for the down-regulated ones. Yet, all of the hub down-regulated miRNAs are reported to have associations with different kinds of cancer.\nCONCLUSION: The introduced hub miRNAs and genes may serve as feasible markers in the mechanisms of H.pylori infection for different kinds of gastric diseases, in particular gastric cancer. However, their role requires further investigations.", "claims": [{"id": "claim-method", "statement": "GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r/), R-based which is a GEO online tool analyzed the differentially expressed microRNAs of the mentioned dataset. Specifically, two groups of samples from four groups were selected for this investigation. The first two groups were cancerous tissue HP+ and HP- while the other two groups were noncancerous regions HP+ and HP-, 32 samples altogether. 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