Title of article :
The Highlighted Roles of Metabolic and Cellular Response to Stress Pathways Engaged in Circulating hsa-miR-494-3p and hsa-miR-661 in Alzheimer’s Disease
Author/Authors :
Hojati ، Zohreh Department of Cell and Molecular Biology and Microbiology, Division of Genetics - Faculty of Biological Science and Technology - University of Isfahan , Omidi ، Farzaneh Department of Genetics - Faculty of Biological Sciences - Tarbiat Modares University , Dehbashi ، Moein Department of Cell and Molecular Biology and Microbiology, Division of Genetics - Faculty of Biological Science and Technology - University of Isfahan , Mohammad Soltani ، Bahram Department of Genetics - Faculty of Biological Sciences - Tarbiat Modares University
From page :
62
To page :
67
Abstract :
Background: Among different roles of miRNAs in AD pathogenesis, hsa-miR-494-3p and hsa-miR-661 functions are poorly understood. Methods: To obtain the gene targets, gene networks, gene ontology, and enrichment analysis of the two miRNAs, some web servers were utilized. Furthermore, the expressions of these miRNAs were analyzed by qRT-PCR in 36 blood sera, including 18 Alzheimer’s patients and 18 healthy individuals. Results: The in silico analysis demonstrated the highlighted roles of metabolic and cellular response to stress pathways engaged in circulating hsa-miR-494-3p and hsa-miR-661 in AD. The qRT-PCR analysis showed that the downregulated expression level of hsa-miR-661 was statistically significant (p 0.05). Also, the ROC curve of hsa-miR-661 displayed the significant AUC (p = 0.01). Conclusion: Based on our findings, the metabolic and cellular responses to stress pathways are closely connected to these two miRNAs functions. Besides, the qRT-PCR and Roc curve determined hsa-miR-661 could be as a biomarker for diagnosis or prognosis of AD patients.
Keywords :
Alzheimer’s disease , Serum , Circulating microRNAs
Journal title :
Iranian Biomedical Journal(IBJ)
Journal title :
Iranian Biomedical Journal(IBJ)
Record number :
2725047
Link To Document :
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