| Literature DB >> 32199199 |
Mahsa Tahmasebivand1, Seyyed Reza Mousavi1, Mehdi Khorrami2, Hormoz Ayromlou3, Reza Rikhtegar4, Leila Saberi2, Bahareh Khademi1, Zahra Bahmanpour1, Babak Emamalizadeh5.
Abstract
Multiple sclerosis is immune-mediated disease of the central nervous system characterized by demyelination in axons. IFN-β is first-line treatment of MS. Biomarkers are needed for early prediction of responders and non-responders to therapy in the first month of treatment to avoid further disabilities. In this study, we analyzed the expression level of miR-504 and miR-711 in 52 IFN-β responder patients in comparison to 53 non-responders. In the next step, the in-silico analysis was used to enrich related signaling pathways. The expression level of miR-504 was significantly higher in patients who respond to IFN-β therapy, compared with non-responders and we obtain related statistically significant KEGG molecular signaling pathways. Our findings suggest that miR-504 can be considered as a novel biomarker for response to IFN-b therapy.Entities:
Keywords: Biomarker; Interferon-beta; Multiple sclerosis; miRNA
Year: 2020 PMID: 32199199 DOI: 10.1016/j.jneuroim.2020.577212
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478