Literature DB >> 31399867

MicroRNA expression profiling provides novel insights into immune-related pathways involved in gastric cancer.

Mário Rino Martins1, Renata Santos Almeida2, Norma Lucena-Silva2, Cláudia Malheiros Coutinho-Camilo3, Israel Torjal3, Rogério Luiz Dos Santos4, Cristiana Libardi Miranda-Furtado5, Álvaro Fabrício Lopes Rios6, Leuridan Cavalcante Torres7, Maria Dirlei F S Begnami8.   

Abstract

Gastric cancer is one of the most common cancers, and an increasing number of studies have found that microRNAs (miRNAs) play essential roles in gastric cancer progression; however, the roles of specific miRNAs involved in the immune response to this disease remain unclear. We compared the miRNA expression in tissues from primary gastric cancer patients and healthy controls to find miRNAs dysregulated in gastric cancer and used bioinformatics tools to determine potential roles of these miRNAs in the immune system. We evaluated 25 primary gastric cancer tissues and five healthy gastric tissues. Quantitative real-time polymerase chain reaction was performed for a set of miRNAs, followed by the prediction of their target genes and functional enrichment analysis of these targets. Analysis of a microarray dataset showed that the miRNA miR-196a-5p was significantly upregulated, while miR-374a-5p and miR-375 were downregulated in gastric cancer patients. In addition, miR-374-5p was significantly downregulated in patients with metastasis compared with its expression levels in non-metastatic patients (p = 0.03). Bioinformatics analysis suggested that the pathways regulated by these differentially expressed miRNAs were related to the immune response, cell adhesion, and cell migration. Most importantly, this study provides a new insight into the potential use of multiple miRNAs to find distinct pathways of immune regulation in gastric cancer.

Entities:  

Keywords:  Bioinformatics; Gastric cancer; Immune system; MicroRNA; Microarray analysis

Mesh:

Substances:

Year:  2019        PMID: 31399867     DOI: 10.1007/s12032-019-1305-x

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  45 in total

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2.  MicroRNA-4290 suppresses PDK1-mediated glycolysis to enhance the sensitivity of gastric cancer cell to cisplatin.

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