Comprehensive analysis of microRNAs and their target genes in oral submucous fibrosis

被引:6
|
作者
Jishnu, Padacherri Vethil [1 ]
Shenoy, Sangeetha U. [1 ]
Sharma, Mohit [2 ]
Chopra, Aditi [3 ]
Radhakrishnan, Raghu [4 ]
机构
[1] Manipal Acad Higher Educ, Manipal Sch Life Sci, Dept Cell & Mol Biol, Manipal, India
[2] SGT Dent Coll Hosp & Res Inst, Dept Oral Pathol, Gurugram, India
[3] Manipal Acad Higher Educ, Manipal Coll Dent Sci, Dept Periodontol, Manipal, India
[4] Manipal Acad Higher Educ, Manipal Coll Dent Sci, Dept Oral Pathol, Manipal 576104, India
关键词
biomarkers; fibrosis; in silico; miRNA; oral cancer; oral submucous fibrosis; BUCCAL MUCOSAL FIBROBLASTS; PATHOGENESIS; MECHANISMS; ARECOLINE; MYOFIBROBLASTS; EXPRESSION; CANCER; CELLS; RISK; BETA;
D O I
10.1111/odi.14219
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The objective of the study is to understand the role of experimentally validated microRNAs (miRNAs) contributing to the acquisition of oncogenic phenotype in oral submucous fibrosis (OSF) by computational analysis. A comprehensive review was carried out to corroborate and summarize altered miRNA expression in OSF by retrieving relevant publications querying MEDLINE, Web of Science, Embase, and Scopus. The association between the miRNA-mRNA was performed using miRTarBase 8.0. The visualization of the miRNA-mRNA interaction was plotted using Cytoscape. MIENTURNET was used for the pathway analysis. Enrichment analysis was carried out for elucidating the hierarchical functions of miRNAs related to the acquisition of biological processes involved in the development of cancer. Thirteen miRNAs (hsa-miR-499a, hsa-miR-200b, hsa-miR-200c, hsa-miR-1246, hsa-miR-31, hsa-miR-10b, hsa-miR-21, hsa-miR-203, hsa-miR-455, hsa-miR-760, hsa-miR-623, hsa-miR-610, and hsa-miR-509-3-5p) were found to be deregulated in OSF. A total of 371 experimentally validated genes were shown to be interacting with the OSF-associated miRNAs. The targets of antifibrotic and profibrotic miRNAs were enriched in the cancer-related pathways. Dysregulated miRNA and its target genes illustrate the physiological role of miRNAs in fibrosis. Understanding the miRNA-mediated fibrotic signaling and targetting the specific miRNA-target gene interaction might provide relevant cues to ameliorate the fibrotic disease.
引用
收藏
页码:1894 / 1904
页数:11
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