<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jin W</submitter><funding>Science Research Foundation of Inner Mongolia People's Hospital</funding><funding>Science and Technology Planning Project for Health of Inner Mongolia</funding><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Inner Mongolia Autonomous Region</funding><pagination>e70014</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11972004</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>MicroRNAs (miRNAs) are crucial factors in gene regulation, and their dysregulation plays important roles in the immunity of gastric cancer (GC). However, finding specific and effective miRNA markers is still a great challenge for GC immunotherapy. In this study, we computed and analysed miRNA-seq, RNA-seq and clinical data of GC patients from the TCGA database. With the comparison of tumour and normal tissues in GC, we identified 2056 upregulated and 2311 downregulated protein-coding genes. Based on the miRNet database, more than 2600 miRNAs interact with these genes. Several key miRNAs, including hsa-mir-34a, hsa-mir-182 and hsa-mir-23b, were identified to potentially play important regulatory roles in the expression of most upregulated and downregulated genes in GC. Based on bioinformation approaches, the expressions of hsa-mir-34a and hsa-mir-182 were closely linked to the tumour stage, and high expression of hsa-mir-23b was correlated with poor survival in GC. Moreover, these three miRNAs are involved in immune cell infiltration (such as activated memory CD4 T cells and resting mast cells), particularly hsa-mir-182 and hsa-mir-23b. GSEA suggested that the changes in their expression may possibly activate/inhibit immune-related signal pathways, such as chemokine signalling pathway and CXCR4 pathway. These results will provide possible miRNA markers or targets for combined immunotherapy of GC.</pubmed_abstract><journal>IET systems biology</journal><pubmed_title>Transcriptome Analyses Reveal the Important miRNAs Involved in Immune Response of Gastric Cancer.</pubmed_title><pmcid>PMC11972004</pmcid><funding_grant_id>62171241</funding_grant_id><funding_grant_id>81960449</funding_grant_id><funding_grant_id>202202024</funding_grant_id><funding_grant_id>62262049</funding_grant_id><funding_grant_id>2021YN18</funding_grant_id><funding_grant_id>2022QN06007</funding_grant_id><pubmed_authors>Cao L</pubmed_authors><pubmed_authors>Jin W</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Yu L</pubmed_authors><pubmed_authors>Feng Z</pubmed_authors><pubmed_authors>Zuo Y</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Yang T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome Analyses Reveal the Important miRNAs Involved in Immune Response of Gastric Cancer.</name><description>MicroRNAs (miRNAs) are crucial factors in gene regulation, and their dysregulation plays important roles in the immunity of gastric cancer (GC). However, finding specific and effective miRNA markers is still a great challenge for GC immunotherapy. In this study, we computed and analysed miRNA-seq, RNA-seq and clinical data of GC patients from the TCGA database. With the comparison of tumour and normal tissues in GC, we identified 2056 upregulated and 2311 downregulated protein-coding genes. Based on the miRNet database, more than 2600 miRNAs interact with these genes. Several key miRNAs, including hsa-mir-34a, hsa-mir-182 and hsa-mir-23b, were identified to potentially play important regulatory roles in the expression of most upregulated and downregulated genes in GC. Based on bioinformation approaches, the expressions of hsa-mir-34a and hsa-mir-182 were closely linked to the tumour stage, and high expression of hsa-mir-23b was correlated with poor survival in GC. Moreover, these three miRNAs are involved in immune cell infiltration (such as activated memory CD4 T cells and resting mast cells), particularly hsa-mir-182 and hsa-mir-23b. GSEA suggested that the changes in their expression may possibly activate/inhibit immune-related signal pathways, such as chemokine signalling pathway and CXCR4 pathway. These results will provide possible miRNA markers or targets for combined immunotherapy of GC.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan-Dec</publication><modification>2025-07-08T03:13:52.739Z</modification><creation>2025-07-08T03:13:52.739Z</creation></dates><accession>S-EPMC11972004</accession><cross_references><pubmed>40186852</pubmed><doi>10.1049/syb2.70014</doi></cross_references></HashMap>